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          "en" => "<p id="spar0065" class="elsevierStyleSimplePara elsevierViewall">High doses of uremic toxins induce the expression of the profibrotic cytokine TGF-&#946;1 and extracellular matrix proteins in vascular smooth muscle cells&#46; Human aortic smooth muscle cells were incubated with medium supplemented with 2&#46;5&#37; human serum for 24<span class="elsevierStyleHsp" style=""></span>h&#46; Subsequently they were treated for 2&#44; 4&#44; 6 or 24<span class="elsevierStyleHsp" style=""></span>h &#40;A&#44; C and D&#41; or 24<span class="elsevierStyleHsp" style=""></span>h &#40;B&#41; with uremic toxins&#58; indoxil-sulfate &#40;IS 100<span class="elsevierStyleHsp" style=""></span>&#956;g&#47;ml&#41;&#44; para-cresol &#40;pc 100<span class="elsevierStyleHsp" style=""></span>&#956;g&#47;ml&#41; or a mixture of both &#40;IS<span class="elsevierStyleHsp" style=""></span>&#43;<span class="elsevierStyleHsp" style=""></span>1pc 100<span class="elsevierStyleHsp" style=""></span>&#956;g&#47;ml&#41;&#46; Representative Western blots of TGF-&#946;1 &#40;A&#41;&#44; collagen I &#40;COL I&#44; C&#41; and fibronectin &#40;D&#41; are shwon&#46; The levels of GAPDH were determined as their respective endogenous controls&#46; The bars represent the values of the densitometric analysis of the normalized blots against the endogenous control&#46; The expression of TGF-&#946;1 was analyzed by immunofluorescence &#40;B&#41;&#46; Representative images of the photographs obtained by confocal microscopy &#40;100&#215;&#41; are shown&#46; The values are represented as the mean<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>SEM&#46; &#42; <span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>0&#46;05 vs&#46; Control &#40;CT&#44; untreated cells&#41;&#46;</p>"
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    "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0075">Introduction</span><p id="par0005" class="elsevierStylePara elsevierViewall">Chronic kidney disease &#40;CKD&#41; is a major health problem&#46; In Spain&#44; it affects approximately to 14&#37; of the population<a class="elsevierStyleCrossRef" href="#bib0145"><span class="elsevierStyleSup">1</span></a> and&#44; in cases of advanced disease&#44; the health cost is disproportionate to its prevalence&#46; It is Important to note that as compared with the general population&#44; patients with CKD have a much higher risk of cardiovascular disease&#46; This can not be explained solely by the high prevalence of classic cardiovascular risk factors such as hypertension&#44; hyperlipidemia&#44; diabetes&#44; smoking or left ventricular hypertrophy&#46;<a class="elsevierStyleCrossRefs" href="#bib0150"><span class="elsevierStyleSup">2&#44;3</span></a> It has been proposed that in CKD&#44; cardiovascular disease is influenced by many other factors such as oxidative stress&#44; which is induced by the uremia itself&#44; alterations of phosphate and calcium metabolism or the accumulation of toxic metabolites capable of producing vascular damage&#46;<a class="elsevierStyleCrossRefs" href="#bib0160"><span class="elsevierStyleSup">4&#44;5</span></a> All these factors produce structural and functional alterations of the cardiovascular system such as endothelium dysfunction&#44;<a class="elsevierStyleCrossRef" href="#bib0170"><span class="elsevierStyleSup">6</span></a> arterial rigidity&#44; the development of arteriosclerotic lesions or vascular calcifications&#44;<a class="elsevierStyleCrossRef" href="#bib0175"><span class="elsevierStyleSup">7</span></a> conditioning tissue ischemia&#44; tissue damage and death&#46; In addition&#44; a common phenomenon&#44; which contributes to progressive renal dysfunction and the vascular damage of arteriosclerosis&#44; is the abnormal accumulation of extracellular matrix &#40;ECM&#41; proteins in large quantities in the renal or vascular structures&#44; which itself causes important alterations in the structure of the kidney and vessels&#46;<a class="elsevierStyleCrossRef" href="#bib0180"><span class="elsevierStyleSup">8</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">A characteristic of CKD is the progressive deterioration of renal function&#44; which often leads to end stage renal disease&#46; In the final stages of CKD&#44; uremia occurs&#44; a situation in which the internal environment is totally altered&#46; Recently identified uremic toxins bound to proteins such as indoxyl sulfate &#40;IS&#41; and para-cresyl sulfate &#40;p-CS&#41; can not be removed by conventional dialysis methods and these are pathogenic agents associated with the cardiovascular mortality in CKD patients and those with more advanced kidney diseases requiring dialysis&#46;<a class="elsevierStyleCrossRef" href="#bib0185"><span class="elsevierStyleSup">9</span></a> Among the undesirable effects of uremic toxins&#44; that are accumulated in the plasma of these patients&#44; are vascular inflammation&#44; endothelial dysfunction and vascular calcifications&#44; which could explain the poor prognosis of dialysis and predialysis patients&#46;<a class="elsevierStyleCrossRef" href="#bib0190"><span class="elsevierStyleSup">10</span></a> Through in vitro studies&#44; it has been observed that IS promotes the proliferation of vascular smooth muscle cells &#40;VSMC&#41;&#44;<a class="elsevierStyleCrossRef" href="#bib0195"><span class="elsevierStyleSup">11</span></a> that together migration and high production of ECM proteins&#44; produces hyperplasia of the neointima&#44; abnormalities in vascular repair and marked reduction of vascular lummen&#46;<a class="elsevierStyleCrossRef" href="#bib0180"><span class="elsevierStyleSup">8</span></a> In addition&#44; the migration and proliferation of VSMC can be stimulated by local inflammation&#44; which can be triggered by IS and other uremic toxins&#44; such as advanced glycation products&#46;<a class="elsevierStyleCrossRef" href="#bib0200"><span class="elsevierStyleSup">12</span></a></p><p id="par0015" class="elsevierStylePara elsevierViewall">The aim of this work was a comprehensive study of the contribution of toxins accumulated in the serum of uremic patients to the vascular damage and&#44; in particular&#44; to the abnormal deposition of ECM in vascular tissue&#46; For this purpose&#44; we have used an animal model of progressive CKD&#44; by feeding the animals an adenine rich diet&#44; or by incubating human aortic smooth muscle cells &#40;HAOSMC&#41; with uremic toxins&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0080">Methods</span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0085">Animal model and determinations</span><p id="par0020" class="elsevierStylePara elsevierViewall">We used 3&#8211;4 month old male mice strain C57BL&#47;6J &#40;Jackson Laboratory&#44; Bar Harbor&#44; Maine&#44; United States&#41;&#46; The control group were mice fed a standard diet during the entire experimental period&#46; In the CKD group&#44; mice were bred as their littermates and were fed a diet containing 0&#46;2&#37; adenine &#40;Sigma&#44; St Louis&#44; MO&#44; United States&#41;&#44; for a period of 2&#44; 4 or 6 weeks&#46;<a class="elsevierStyleCrossRef" href="#bib0205"><span class="elsevierStyleSup">13</span></a> Basal &#40;week 0&#41; or 2 and 4 week blood samples were collected by incision of a lower palpebral vein&#46; All other parameters were analyzed at weeks 0&#44; 2&#44; 4 and 6 of the experimental period&#44; when the mice were euthanized&#46; One day before sacrifice&#44; the animals were housed in metabolic cages to collect 24<span class="elsevierStyleHsp" style=""></span>h urine&#46; Then&#44; the mice were anesthetized with ketamine&#8211;xylazine &#40;100&#47;20<span class="elsevierStyleHsp" style=""></span>mg&#47;kg&#44; i&#46;p&#46;&#41;&#44; underwent a thoracotomy and were exsanguinated through a cut in the right atrium&#46; The aorta was removed and fixed in a buffered solution of 10&#37; formaldehyde&#44; dehydrated and included in paraffin according to the conventional histological technique&#44;<a class="elsevierStyleCrossRef" href="#bib0210"><span class="elsevierStyleSup">14</span></a> or it was stored at &#8722;80<span class="elsevierStyleHsp" style=""></span>&#176;C for the RT-qPCR assays&#46; For the latter&#44; the total RNA of each sample was extracted with TRIzol&#44; transcribed into cDNA&#44; and 10<span class="elsevierStyleHsp" style=""></span>ng were amplified with TaqMan probes for &#946;-actin or by SYBR Green Master Mix &#40;Life Technologies&#44; Waltham&#44; MA&#44; United States&#41; with designed primers using the PubMed database&#58; TGF-&#946;1&#44; 5&#8242;-TTGCTTCAGCTCCACAGAGA-3&#8242; &#40;forward&#41; and 5&#8242;-TGGTTGTAGAGGGCAAGGAC-3&#8242; &#40;reverse&#41;&#59; fibronectin&#44; 5&#8242;-TGAGCGCCCTAAAGATTCCA-3&#8242; &#40;forward&#41; and 5&#8242;-TAGCCACCAGTCTCATGTGC-3&#8242; &#40;reverse&#41;&#59; collagen type I&#44; 5&#8242;-TCCTGGCAACAAAGGAGACA-3&#8242; &#40;forward&#41; and 5&#8242;-GGGCTCCTGGTTTTCCTTCT-3&#8242; &#40;reverse&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0210"><span class="elsevierStyleSup">14</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">The plasma and urinary chemistries&#44; creatinine and the plasma urea nitrogen&#44; were measured using commercial kits&#44; according to the manufacturer&#39;s instructions &#40;Arbor Assays LLC&#44; Ann Arbor&#44; MI&#44; United States&#41;&#46; The values of plasma and urinary concentration of the sodium ion &#40;Sodium Assay Kit&#44; Abcam&#44; Cambridge&#44; United Kingdom&#41; were used to calculate the fractional excretion of sodium&#46; The spectrophotometric determinations were carried out with the Victor Multimode Plate Reader Victor X4 &#40;PerkinElmer&#44; Waltham&#44; MA&#44; United States&#41;&#46;</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0090">Incubation with uremic toxins&#46; Parameters measured</span><p id="par0030" class="elsevierStylePara elsevierViewall">The HAOSMC were obtained by enzymatic dissociation of the aorta from 5 organ donors&#44; in accordance with the Spanish legal provisions&#44; with the approval of the Ethical Committee of the University Hospital of Getafe as previously described&#46;<a class="elsevierStyleCrossRef" href="#bib0215"><span class="elsevierStyleSup">15</span></a> These were generously donated by Dr&#46; S&#225;nchez-Ferrer&#46; The cells were maintained in DMEM culture medium supplemented with 10&#37; calf serum&#44; <span class="elsevierStyleSmallCaps">l</span>-glutamine&#44; amphotericin&#44; penicillin and streptomycin&#46; For the experiments&#44; the HAOSMC&#44; passages 3&#8211;10&#44; were cultured with 2&#46;5&#37; human serum &#40;AB serum&#59; BioWhittaker&#44; Walkersville&#44; MD&#44; United States&#41; for 24<span class="elsevierStyleHsp" style=""></span>h and incubated with the uremic solutes p-cresol &#40;pc&#41; and IS &#40;Sigma&#41;&#44; at concentrations of the uremic range &#40;IS&#58; 25 and 100<span class="elsevierStyleHsp" style=""></span>&#956;g&#47;ml and pc 10 and 100<span class="elsevierStyleHsp" style=""></span>&#956;g&#47;ml&#41;&#44; alone or combined together at low or high concentrations during a variable period of time&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">Once the treatments were finished&#44; the cell protein content was quantified by conventional Western blot<a class="elsevierStyleCrossRef" href="#bib0220"><span class="elsevierStyleSup">16</span></a> using primary antibodies against TGF-&#946;1&#44; collagen I or fibronectin &#40;Cell Signaling Technology&#44; Danvers&#44; MA&#44; United States&#41;&#46; The TGF-&#946;1 was also evaluated by immunofluorescence using confocal microscopy &#40;Leica17&#41;&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0095">Statistic analysis</span><p id="par0040" class="elsevierStylePara elsevierViewall">All the data was analyzed with the GraphPad Prism software&#46; The results are expressed as the mean<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>SEM&#46; As the number of animals or experiments was never greater than 10&#44; the comparisons were made for nonparametric data&#44; applying the Kruskal&#8211;Wallis test with Mann&#8211;Whitney post-test &#40;unpaired data&#41; or the Friedman test with Wilcoxon post test &#40;paired data&#41;&#46; A <span class="elsevierStyleItalic">p</span> value &#60;0&#46;05 was considered significant&#46;</p></span></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0100">Results</span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0105">Mice feed an adenine rich diet simultaneously develop chronic kidney disease and vascular damage&#46;</span><p id="par0045" class="elsevierStylePara elsevierViewall">In the mice experiments&#44; progressive CKD was generated by feeding the animals an adenine rich diet and the measurements were obtained at 2&#44; 4 or 6 weeks&#46; First&#44; the generation of CKD was illustrated by the change in parameters that are presented in <a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>&#46; Animals fed adenine rich diet exhibited a progressive increase in plasma creatinine and urea nitrogen concentrations&#44; as well as alterations in the handling of sodium and water&#44; manifested by the increase in diuresis and in the fractional excretion of sodium&#46; These changes were significant at 2 weeks and progressively worsens with the prolongation of the adenine administration &#40;<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>&#41;&#46; Next&#44; the possible vascular abnormalities were evaluated&#46; The changes in the vascular structure of the aortas that could be produced by progressive CKD were investigated by microscopic examination&#46; Mice with CKD induced by 6 weeks of adenine rich diet presented a thickening of the media layer and a moderate decrease of the radius of lummen &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 1</a>&#41;&#46; The morphometric analysis indicated that the thickness of the media is significantly higher in animals on Adenine than Controls&#46; In these two groups&#44; the radius of the lumen was not significantly different although it tends to be reduced in animals on adenine rich diet&#46; Therefore&#44; in these mice there was significant increase in the ratio media&#47;radius of lummen&#46; In addition&#44; uremic animals showed a progressive increase in the expression of the profibrotic cytokine TGF-&#946;1&#44; as well as the ECM proteins collagen type I and fibronectin&#44; tissue fibrosis markers as determined by RT-qPCR of the mice aortas &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 2</a>A and C&#41;&#44; which was significant for the 3 time periods in the case of TGF-&#946;1 and from week 4 for the ECM proteins&#46;</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0110">In cultured human aortic smooth muscle cells &#40;HAOSMC&#41; uremic toxins induce the expression of the profibrotic cytokine TGF-&#946;1 and extracellular matrix protein</span><p id="par0050" class="elsevierStylePara elsevierViewall">In vitro tests were performed using HAOSMC cells aiming to identify the mechanisms whereby uremic rats developed thickening of the aorta&#39;s wall&#46; We use a model developed in our laboratory that simulate in part the environment of uremia in moderate or advanced CKD by adding low&#44; high doses or mixtures of 2 uremic toxins &#40;IS and pc&#41; to the culture medium&#46; First&#44; cell viability assessed by MTT assays&#44; was demonstrated while on treatment with uremic toxins&#44; at the doses and times used&#44; by means of &#40;data not shown&#41;&#46; Second&#44; it was observed that uremic toxins induce a time and dose-dependent increase in TGF-&#946;1 expression&#44; after incubation with high doses&#44; of one or the two uremic toxins combined&#44; as determined by Western blot and immunofluorescence &#40;<a class="elsevierStyleCrossRef" href="#fig0020">Fig&#46; 3</a>A&#44; B&#41;&#46; The increase in TGF-&#946;1 expression was significant at 4<span class="elsevierStyleHsp" style=""></span>h of treatment&#46; The effect of both uremic toxins on TGF-&#946;1 expression is additive&#44; since the incubation with high doses of the two compounds simultaneously produces a significantly further increase in TGF-&#946;1 expression as compared with the separate treatment with each of the toxins &#40;Supplementary Fig&#46; 1A&#41;&#46; On the other hand&#44; the incubation with the toxins at low doses&#44; whether used separately or simultaneously&#44; does not induce changes in the expression of this cytokine &#40;data not shown&#41;&#46; In parallel&#44; the incubation with the high concentration of uremic toxins produced an increase in the expression of the ECN proteins&#44; collagen I and fibronectin&#44; that is significant at 2 and 4<span class="elsevierStyleHsp" style=""></span>h of treatment&#44; respectively &#40;<a class="elsevierStyleCrossRef" href="#fig0020">Fig&#46; 3</a>C and D&#41;&#46; Once again&#44; the effect is greater if the toxins are used in combination &#40;Supplementary Fig&#46; 1B and C&#41;&#46;</p><elsevierMultimedia ident="fig0020"></elsevierMultimedia></span></span><span id="sec0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0115">Discussion</span><p id="par0055" class="elsevierStylePara elsevierViewall">The main findings of this study are that uremia induces the expression of the profibrotic cytokine TGF-&#946;1 with the accumulation of ECM proteins in the aortas of mice with progressive uremia induced by adenine rich diet&#46; Also&#44; we show that uremic toxins induce the expression of these proteins in cultured HAOSMC cells&#46;</p><p id="par0060" class="elsevierStylePara elsevierViewall">Although there have been numerous studies aiming to identify CKD factors that could produce cardiovascular diseases&#44; there are few studies analyzing pathophysiological mechanisms whereby uremia induces accumulation of ECM proteins in the wall of large vessels leading cardiovascular damage in CKD patients&#46; Several studies have demonstrated the contribution of uremic toxins to vascular dysfunction&#44; but often the mechanisms involved are not clear&#46; It has been shown that IS stimulates the proliferation of VSMC through the production of reactive oxygen species&#44;<a class="elsevierStyleCrossRefs" href="#bib0195"><span class="elsevierStyleSup">11&#44;18</span></a> and it has been observed that the administration of this toxin promotes calcification and thickening of the aortic wall in hypertensive rats&#46;<a class="elsevierStyleCrossRef" href="#bib0235"><span class="elsevierStyleSup">19</span></a> In CKD patients&#44; vascular calcifications are observed particularly in the media&#44; also in the elastic fibers and surrounding the VSMC&#46;<a class="elsevierStyleCrossRef" href="#bib0240"><span class="elsevierStyleSup">20</span></a> It has been observed that the deposition of matrix in the artery wall my result from an active cellular process that involves the transdifferentiation of the VSMC into a cell type similar to the osteoblasts&#44; which leads to the deposit of ECM of osteogenic type&#44; a process that also it is induced by IS in vitro&#46;<a class="elsevierStyleCrossRef" href="#bib0245"><span class="elsevierStyleSup">21</span></a> Additionally&#44; both IS and p-CS induce cell dedifferentiation and renal fibrosis&#44; via epithelial&#8211;mesenchymal transition&#44; both in vitro and in vivo&#46;<a class="elsevierStyleCrossRefs" href="#bib0250"><span class="elsevierStyleSup">22&#44;23</span></a> However&#44; as far as we know&#44; the present work is the first that directly relates these uremic toxins with the increased production of profibrotic cytokines and fibrillar type ECM by HAOSMC&#46;</p><p id="par0065" class="elsevierStylePara elsevierViewall">Multiple studies have shown the importance of TGF-&#946;1 in the progression of CKD&#46;<a class="elsevierStyleCrossRef" href="#bib0260"><span class="elsevierStyleSup">24</span></a> Our research group has been interested for years in the study of the mechanisms responsible for the development and progression of tissue damage in cardiovascular and renal diseases&#46; The conceptual approach to the study of these mechanisms has been carried out from different perspectives&#44; but one of the possibilities is that the accumulation of ECM proteins&#44; at renal or vascular level&#44; may condition a positive feedback&#44; which leads to a worsening of the situation or a greater tissue damage&#46; We have reported that the contact of renal mesangial cells with abnormal collagens induces the synthesis of TGF-&#946;1<a class="elsevierStyleCrossRef" href="#bib0265"><span class="elsevierStyleSup">25</span></a> and the production of TGF-&#946;1 is also stimulated by free radicals&#44;<a class="elsevierStyleCrossRef" href="#bib0225"><span class="elsevierStyleSup">17</span></a> and that in both cases&#44; the fibrotic process self-perpetuates&#44; increasing the expression of ECM proteins&#44; such as collagen I and IV and fibronectin&#44;<a class="elsevierStyleCrossRefs" href="#bib0225"><span class="elsevierStyleSup">17&#44;25</span></a> which favor the progression of CKD&#46; In the resent study we have shown a direct relationship between solutes that accumulate in the serum of uremic patients such as protein bound uremic toxins&#44; IS and pc&#44; and the production of TGF-&#946;1 and MEC by HAOSMC&#46; It is possible that the origin of this phenomenon is the increase of reactive oxygen species induced by uremic toxins&#44; a phenomenon described in vascular endothelial cells by others and ourselves&#44;<a class="elsevierStyleCrossRefs" href="#bib0180"><span class="elsevierStyleSup">8&#44;16</span></a> in monocytes and macrophages&#44;<a class="elsevierStyleCrossRef" href="#bib0180"><span class="elsevierStyleSup">8</span></a> in renal tubule cells<a class="elsevierStyleCrossRef" href="#bib0240"><span class="elsevierStyleSup">20</span></a> and in rat VSMC&#44;<a class="elsevierStyleCrossRef" href="#bib0230"><span class="elsevierStyleSup">18</span></a> and that we have verified in the in vitro uremia model used in this work &#40;data not shown&#41;&#46;</p><p id="par0070" class="elsevierStylePara elsevierViewall">In addition&#44; we have explored the additive effect of the two toxins&#44; IS and pc&#44; as previously observed when p-CS is combined with para-cresyl glucuronide&#46;<a class="elsevierStyleCrossRef" href="#bib0270"><span class="elsevierStyleSup">26</span></a> A possible limitation in the clinical translation of any of our results is the use of the PC acting as a substitute for p-CS&#44; a PC derivative by sulfation which is its main circulating metabolite&#46; PC was for a long time considered one of the main uremic toxins&#44; but it is currently known to circulate freely in plasma in very low amounts&#44; and that the main cresols that are actually retained in uremia are p-CS and para-cresil glucuronide&#44; the other conjugate of pc&#46;<a class="elsevierStyleCrossRef" href="#bib0275"><span class="elsevierStyleSup">27</span></a> We have used a rat model of uremia in which animals are maintained on a diet containing high amounts of Adenine which causes nephrotoxicity when metabolized to 2&#44;8-dihydroxyadenine&#44; an insoluble compound that precipitates in the renal tubules as crystals&#44; producing tubule occlusion&#44; inflammation and tubuloinsterstitial fibrosis&#46;<a class="elsevierStyleCrossRef" href="#bib0205"><span class="elsevierStyleSup">13</span></a> Since functional and structural alterations are similar to those observed in CKD and occur gradually and progressively&#44; this model has been very useful to examine the pathophysiological mechanisms that cause cardiovascular disease in CKD&#46; In fact&#44; in the aortas of these animals we have observed a thickening of the media&#44; which is also observed in coronary arteries of uremic patients&#44; as well as the thickening of the intima-media of carotid arteries&#46;<a class="elsevierStyleCrossRef" href="#bib0180"><span class="elsevierStyleSup">8</span></a> In addition&#44; we found a progressive accumulation of ECM proteins in the aortic wall&#44; a process that has been related&#44; together with the decrease in elastin levels&#44; with the arterial remodeling characterized by stiffness of the aorta and the major arteries&#44; whose main pathophysiological consequence is the loss of arterial distensibility&#46;<a class="elsevierStyleCrossRef" href="#bib0180"><span class="elsevierStyleSup">8</span></a></p><p id="par0075" class="elsevierStylePara elsevierViewall">Finally&#44; the concentrations of toxins that we use in this study are within the range reported in uremic patients &#40;1&#8211;100<span class="elsevierStyleHsp" style=""></span>&#956;g&#47;ml&#41;&#44;<a class="elsevierStyleCrossRef" href="#bib0280"><span class="elsevierStyleSup">28</span></a> but in uremic patients the values of these uremic toxins could be has high as 236 and 105<span class="elsevierStyleHsp" style=""></span>&#956;g&#47;ml for the IS and p-CS respectively&#44; in hemodialysis patients&#44;<a class="elsevierStyleCrossRef" href="#bib0280"><span class="elsevierStyleSup">28</span></a> and less than 4&#46;9 and 46<span class="elsevierStyleHsp" style=""></span>&#956;g&#47;ml for IS and p-CS respectively&#44; in patients with CKD not on dialysis&#44; for whom there is very scarce information&#46;<a class="elsevierStyleCrossRef" href="#bib0220"><span class="elsevierStyleSup">16</span></a> In addition&#44; higher levels of both toxins have been observed in patients with CKD stages 1&#8211;5 that are progressor vs&#46; the non progressors&#46;<a class="elsevierStyleCrossRef" href="#bib0220"><span class="elsevierStyleSup">16</span></a> Results from in vitro and in vivo experiments&#44; indicate that there is a significant increase in the production and&#47;or accumulation of ECM proteins when exposed to high concentration the uremic toxins&#44; or after 4 weeks of high adenine diet&#46;</p></span><span id="sec0050" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0120">Conclusion</span><p id="par0080" class="elsevierStylePara elsevierViewall">The present work demonstrates for the first time that uremic toxins that accumulate in patients with end stage kidney diseases induce the expression of the cytokine TGF-&#946;1 and proteins of ECM by the HAOSMC&#46; This could explain the mechanism of vascular damage and ECM accumulation observed in vivo in the model of progressive CKD induced by adenine rich diet&#46;</p></span><span id="sec0055" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0125">Financing</span><p id="par0085" class="elsevierStylePara elsevierViewall">This work has been financed by the <span class="elsevierStyleGrantSponsor" id="gs1">Carlos III Health Institute &#40;ISCIII&#41;</span> and <span class="elsevierStyleGrantSponsor" id="gs2">FEDER</span> funds &#40;<span class="elsevierStyleGrantNumber" refid="gs2">PI14&#47;02075</span>&#44; <span class="elsevierStyleGrantNumber" refid="gs2">PI17&#47;00625</span>&#44; <span class="elsevierStyleGrantNumber" refid="gs2">PI17&#47;01513</span>&#41;&#44; <span class="elsevierStyleGrantSponsor" id="gs3">FEDER funds and ISCIII RETIC REDinREN</span> programs &#40;<span class="elsevierStyleGrantNumber" refid="gs3">RD12&#47;0021&#47;0006</span> and <span class="elsevierStyleGrantNumber" refid="gs3">RD16&#47;0009&#47;0018</span>&#41;&#44; <span class="elsevierStyleGrantSponsor" id="gs4">Autonomous Community of Madrid</span> &#40;NOVELREN-CM REF&#58; <span class="elsevierStyleGrantNumber" refid="gs4">B2017&#47;BMD-3751</span>&#41;&#44; <span class="elsevierStyleGrantSponsor" id="gs5">University of Alcal&#225;</span> &#40;<span class="elsevierStyleGrantNumber" refid="gs5">CCG2016&#47;BIO-043</span>&#41; and the <span class="elsevierStyleGrantSponsor" id="gs6">Senefro Foundation</span> &#40;Senefro-2016&#41; to LCB&#44; and <span class="elsevierStyleGrantSponsor" id="gs7">Renal Foundation I&#241;igo &#193;lvarez de Toledo &#40;FRIAT&#41;</span>&#46;</p></span><span id="sec0060" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0130">Authorship</span><p id="par0090" class="elsevierStylePara elsevierViewall">Diego Rodr&#237;guez-Puyol and Laura Calleros share the direction of this work&#46;</p></span><span id="sec0065" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0135">Conflicts of interest</span><p id="par0095" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest&#46;</p></span></span>"
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              "titulo" => "Mice feed an adenine rich diet simultaneously develop chronic kidney disease and vascular damage&#46;"
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              "titulo" => "In cultured human aortic smooth muscle cells &#40;HAOSMC&#41; uremic toxins induce the expression of the profibrotic cytokine TGF-&#946;1 and extracellular matrix protein"
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            1 => "Vascular damage"
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            0 => "Enfermedad renal cr&#243;nica"
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        "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Background</span><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Patients with chronic kidney disease present with an accumulation of uremic toxins&#44; which have been identified as pathogenic agents associated with cardiovascular mortality&#44; which is very high is this patient group&#46; A phenomenon common to the progressive renal dysfunction and associated vascular damage&#44; is the abnormal accumulation of extracellular matrix &#40;ECM&#41; proteins in the renal or vascular structures&#46;</p></span> <span id="abst0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Objective</span><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">To determine the contribution of uremia or the uremic toxins to the production of cytokinins and ECM in aortas of uremic animals or human aortic smooth muscle cells &#40;HASMCs&#41;&#46;</p></span> <span id="abst0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Materials and methods</span><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Mice were used with uremia induced by a diet rich in adenine &#40;0&#46;2&#37;&#41; for 2&#44; 4 or 6 weeks&#46; Kidney function was evaluated by means of urine volume&#44; plasma levels of creatinine&#44; urea&#44; fractional excretion of sodium&#44; and vascular damage using histology&#44; as well as protein expression using RT-qPCR&#46; The HASMCs were incubated in vitro with uremic toxins&#58; p-cresol 10&#8211;100 &#40;&#956;g&#47;ml&#41; and indoxyl-sulphate 25&#8211;100 &#40;&#956;g&#47;ml&#41; alone or simultaneously&#46; The protein expression was evaluated using Western blot and confocal microscopy&#46;</p></span> <span id="abst0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Results</span><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">The administration of adenine produced progressive kidney damage in the mice&#44; thickening of the aortic wall&#44; and increasing the expression of TGF-&#946;1 and ECM proteins&#46; The toxins at high doses and combined also induced the expression of TGF-&#946;1 and ECM proteins by the HASMCs&#46;</p></span> <span id="abst0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Conclusions</span><p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">The uremia produced by an adenine rich diet or high doses of uremic toxins induced the abnormal deposit of ECM proteins in the vascular wall or its production by HASMCs&#46; The understanding of the mechanisms that underlie this pathophysiological process may be useful in the prevention of cardiovascular damage associated with the progress of chronic kidney disease&#44; a disease&#44; at the moment that is irreversible and occasional silent until its diagnosis in advanced stages&#46;</p></span>"
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        "resumen" => "<span id="abst0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">Antecedentes</span><p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">Los pacientes con enfermedad renal cr&#243;nica presentan una acumulaci&#243;n de toxinas ur&#233;micas&#44; las cuales han sido identificadas como agentes patog&#233;nicos asociados con la mortalidad cardiovascular&#44; muy elevada en este grupo de enfermos&#46; Un fen&#243;meno com&#250;n a la disfunci&#243;n renal progresiva y al da&#241;o vascular asociado es la acumulaci&#243;n anormal de prote&#237;nas de la matriz extracelular &#40;MEC&#41; en las estructuras renales o vasculares&#46;</p></span> <span id="abst0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">Objetivo</span><p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">Estudiar la contribuci&#243;n de la uremia o las toxinas ur&#233;micas a la producci&#243;n de citocinas y MEC en aortas de animales ur&#233;micos o c&#233;lulas de m&#250;sculo liso de aorta humana &#40;HAOSMC&#41;&#46;</p></span> <span id="abst0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0050">Materiales y m&#233;todos</span><p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">Se utilizaron ratones con uremia inducida por una dieta rica en adenina &#40;0&#44;2&#37;&#41; durante 2&#44; 4 o 6 semanas&#46; Se evalu&#243; la funci&#243;n renal mediante la diuresis&#44; los niveles plasm&#225;ticos de creatinina y nitr&#243;geno ureico plasm&#225;tico&#44; y la excreci&#243;n fraccional de sodio y el da&#241;o vascular mediante histolog&#237;a y expresi&#243;n proteica por RT-qPCR&#46; <span class="elsevierStyleItalic">In vitro</span>&#44; las HAOSMC se incubaron con toxinas ur&#233;micas&#58; p-cresol 10-100 &#40;&#956;g&#47;ml&#41; e indoxil-sulfato 25-100 &#40;&#956;g&#47;ml&#41;&#44; solas o simult&#225;neamente&#46; La expresi&#243;n proteica se evalu&#243; por Western blot y microscopia confocal&#46;</p></span> <span id="abst0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0055">Resultados</span><p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">La administraci&#243;n de adenina produjo un progresivo da&#241;o renal en los ratones&#44; un engrosamiento de la pared a&#243;rtica y un incremento de la expresi&#243;n de TGF-&#946;1 y prote&#237;nas de MEC&#46; Las toxinas a dosis altas y combinadas tambi&#233;n indujeron expresi&#243;n de TGF-&#946;1 y prote&#237;nas de MEC por las c&#233;lulas HAOSMC&#46;</p></span> <span id="abst0050" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0060">Conclusiones</span><p id="spar0050" class="elsevierStyleSimplePara elsevierViewall">La uremia producida por una dieta rica en adenina o las dosis altas de toxinas ur&#233;micas indujeron el dep&#243;sito anormal de prote&#237;nas de MEC en las paredes vasculares o su producci&#243;n por HAOSMC&#46; La comprensi&#243;n de los mecanismos que subyacen a este proceso fisiopatol&#243;gico puede resultar de utilidad en la prevenci&#243;n del da&#241;o cardiovascular asociado a la progresi&#243;n de la enfermedad renal cr&#243;nica&#44; una dolencia&#44; de momento&#44; irreversible y&#44; en ocasiones&#44; silenciosa hasta su diagn&#243;stico en etapas avanzadas&#46;</p></span>"
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        "nota" => "<p class="elsevierStyleNotepara" id="npar0015">Please cite this article as&#58; Hatem-Vaquero M&#44; de Frutos S&#44; Luengo A&#44; Gonz&#225;lez Abajo A&#44; Griera M&#44; Rodr&#237;guez-Puyol M&#44; et al&#46; Contribuci&#243;n de las toxinas ur&#233;micas a la fibrosis vascular asociada a la enfermedad renal cr&#243;nica&#46; Nefrologia&#46; 2018&#59;38&#58;639&#8211;646&#46;</p>"
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            "etiqueta" => "Appendix A"
            "titulo" => "Supplementary data"
            "identificador" => "sec0075"
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          "en" => "<p id="spar0055" class="elsevierStyleSimplePara elsevierViewall">Mice with CKD induced by adenine-rich diet develop vascular structural damage&#46; Mice were fed standard diet &#40;Control&#41; or rich in adenine &#40;adenine&#41; during 6 weeks&#46; &#40;A&#41; The aortas were stained with hematoxylin-eosin&#46; Representative changes are shown&#46; In Control mice&#44; no lesions are seen&#46; Note the thickening of the media &#40;asterisk&#41; of the aortas of the mice fed with Adenine&#46; Scale bar&#58; 100<span class="elsevierStyleHsp" style=""></span>&#956;m&#46; Magnification 20&#215;&#46; &#40;B&#41; Morphometric analysis of the thickness of the media and the radius of the lumen&#44; made by the ImageJ software and calculation of its ratio&#46; The mean of 5 independent measurements in different directions is considered mean radius&#46; The values are presented as the mean<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>SEM&#46; <span class="elsevierStyleSup">1</span><span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>0&#46;05 vs&#46; Control&#46; <span class="elsevierStyleItalic">n</span><span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>5 animals&#47;group&#46;</p>"
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          "en" => "<p id="spar0065" class="elsevierStyleSimplePara elsevierViewall">High doses of uremic toxins induce the expression of the profibrotic cytokine TGF-&#946;1 and extracellular matrix proteins in vascular smooth muscle cells&#46; Human aortic smooth muscle cells were incubated with medium supplemented with 2&#46;5&#37; human serum for 24<span class="elsevierStyleHsp" style=""></span>h&#46; Subsequently they were treated for 2&#44; 4&#44; 6 or 24<span class="elsevierStyleHsp" style=""></span>h &#40;A&#44; C and D&#41; or 24<span class="elsevierStyleHsp" style=""></span>h &#40;B&#41; with uremic toxins&#58; indoxil-sulfate &#40;IS 100<span class="elsevierStyleHsp" style=""></span>&#956;g&#47;ml&#41;&#44; para-cresol &#40;pc 100<span class="elsevierStyleHsp" style=""></span>&#956;g&#47;ml&#41; or a mixture of both &#40;IS<span class="elsevierStyleHsp" style=""></span>&#43;<span class="elsevierStyleHsp" style=""></span>1pc 100<span class="elsevierStyleHsp" style=""></span>&#956;g&#47;ml&#41;&#46; Representative Western blots of TGF-&#946;1 &#40;A&#41;&#44; collagen I &#40;COL I&#44; C&#41; and fibronectin &#40;D&#41; are shwon&#46; The levels of GAPDH were determined as their respective endogenous controls&#46; The bars represent the values of the densitometric analysis of the normalized blots against the endogenous control&#46; The expression of TGF-&#946;1 was analyzed by immunofluorescence &#40;B&#41;&#46; Representative images of the photographs obtained by confocal microscopy &#40;100&#215;&#41; are shown&#46; The values are represented as the mean<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>SEM&#46; &#42; <span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>0&#46;05 vs&#46; Control &#40;CT&#44; untreated cells&#41;&#46;</p>"
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                      "titulo" => "Epidemiology of chronic renal disease in the Galicia population&#58; results of the pilot Spanish EPIRCE study"
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                          "colaboracion" => "on behalf of the EPIRCE study group"
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                        "fecha" => "2005"
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                            2 => "D&#46; Fan"
                            3 => "C&#46;E&#46; McCulloch"
                            4 => "C&#46;Y&#46; Hsu"
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                        "paginaInicial" => "1296"
                        "paginaFinal" => "1305"
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                          "autores" => array:3 [
                            0 => "R&#46;N&#46; Foley"
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                            2 => "M&#46;J&#46; Sarnak"
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                        "tituloSerie" => "J Am Soc Nephrol"
                        "fecha" => "1998"
                        "volumen" => "9"
                        "paginaInicial" => "S16"
                        "paginaFinal" => "S23"
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                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/11443763"
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                      "titulo" => "Urea-induced ROS generation causes insulin resistance in mice with chronic renal failure"
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                          "autores" => array:6 [
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Short Original
Contribution of uremic toxins to the vascular fibrosis associated with chronic kidney disease
Contribución de las toxinas urémicas a la fibrosis vascular asociada a la enfermedad renal crónica
Marco Hatem-Vaqueroa,b,c,d, Sergio de Frutosa,b,c,d, Alicia Luengoa,b,c, Alba González Abajob,c,d,e, Mercedes Grieraa,b,c,d, Manuel Rodríguez-Puyola,b,c, Diego Rodríguez-Puyolb,c,d,e,f, Laura Callerosa,b,c,d,
Corresponding author
laura.calleros@uah.es

Corresponding author.
a Departamento de Biología de Sistemas, Universidad de Alcalá, Alcalá de Henares, Madrid, Spain
b Fundación Renal Íñigo Álvarez de Toledo (FRIAT), Madrid, Spain
c Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), Madrid, Spain
d Red de Investigación Renal (REDinREN), Instituto de Salud Carlos III, Madrid, Spain
e Sección de Nefrología y Fundación para la Investigación, Hospital Universitario Príncipe de Asturias, Alcalá de Henares, Madrid, Spain
f Departamento de Medicina y Especialidades Médicas, Universidad de Alcalá, Alcalá de Henares, Madrid, Spain
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cardiovascular disease is influenced by many other factors such as oxidative stress&#44; which is induced by the uremia itself&#44; alterations of phosphate and calcium metabolism or the accumulation of toxic metabolites capable of producing vascular damage&#46;<a class="elsevierStyleCrossRefs" href="#bib0160"><span class="elsevierStyleSup">4&#44;5</span></a> All these factors produce structural and functional alterations of the cardiovascular system such as endothelium dysfunction&#44;<a class="elsevierStyleCrossRef" href="#bib0170"><span class="elsevierStyleSup">6</span></a> arterial rigidity&#44; the development of arteriosclerotic lesions or vascular calcifications&#44;<a class="elsevierStyleCrossRef" href="#bib0175"><span class="elsevierStyleSup">7</span></a> conditioning tissue ischemia&#44; tissue damage and death&#46; In addition&#44; a common phenomenon&#44; which contributes to progressive renal dysfunction and the vascular damage of arteriosclerosis&#44; is the abnormal accumulation of extracellular matrix &#40;ECM&#41; proteins in large quantities in the renal or vascular structures&#44; which itself causes important alterations in the structure of the kidney and vessels&#46;<a class="elsevierStyleCrossRef" href="#bib0180"><span class="elsevierStyleSup">8</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">A characteristic of CKD is the progressive deterioration of renal function&#44; which often leads to end stage renal disease&#46; In the final stages of CKD&#44; uremia occurs&#44; a situation in which the internal environment is totally altered&#46; Recently identified uremic toxins bound to proteins such as indoxyl sulfate &#40;IS&#41; and para-cresyl sulfate &#40;p-CS&#41; can not be removed by conventional dialysis methods and these are pathogenic agents associated with the cardiovascular mortality in CKD patients and those with more advanced kidney diseases requiring dialysis&#46;<a class="elsevierStyleCrossRef" href="#bib0185"><span class="elsevierStyleSup">9</span></a> Among the undesirable effects of uremic toxins&#44; that are accumulated in the plasma of these patients&#44; are vascular inflammation&#44; endothelial dysfunction and vascular calcifications&#44; which could explain the poor prognosis of dialysis and predialysis patients&#46;<a class="elsevierStyleCrossRef" href="#bib0190"><span class="elsevierStyleSup">10</span></a> Through in vitro studies&#44; it has been observed that IS promotes the proliferation of vascular smooth muscle cells &#40;VSMC&#41;&#44;<a class="elsevierStyleCrossRef" href="#bib0195"><span class="elsevierStyleSup">11</span></a> that together migration and high production of ECM proteins&#44; produces hyperplasia of the neointima&#44; abnormalities in vascular repair and marked reduction of vascular lummen&#46;<a class="elsevierStyleCrossRef" href="#bib0180"><span class="elsevierStyleSup">8</span></a> In addition&#44; the migration and proliferation of VSMC can be stimulated by local inflammation&#44; which can be triggered by IS and other uremic toxins&#44; such as advanced glycation products&#46;<a class="elsevierStyleCrossRef" href="#bib0200"><span class="elsevierStyleSup">12</span></a></p><p id="par0015" class="elsevierStylePara elsevierViewall">The aim of this work was a comprehensive study of the contribution of toxins accumulated in the serum of uremic patients to the vascular damage and&#44; 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St Louis&#44; MO&#44; United States&#41;&#44; for a period of 2&#44; 4 or 6 weeks&#46;<a class="elsevierStyleCrossRef" href="#bib0205"><span class="elsevierStyleSup">13</span></a> Basal &#40;week 0&#41; or 2 and 4 week blood samples were collected by incision of a lower palpebral vein&#46; All other parameters were analyzed at weeks 0&#44; 2&#44; 4 and 6 of the experimental period&#44; when the mice were euthanized&#46; One day before sacrifice&#44; the animals were housed in metabolic cages to collect 24<span class="elsevierStyleHsp" style=""></span>h urine&#46; Then&#44; the mice were anesthetized with ketamine&#8211;xylazine &#40;100&#47;20<span class="elsevierStyleHsp" style=""></span>mg&#47;kg&#44; i&#46;p&#46;&#41;&#44; underwent a thoracotomy and were exsanguinated through a cut in the right atrium&#46; The aorta was removed and fixed in a buffered solution of 10&#37; formaldehyde&#44; dehydrated and included in paraffin according to the conventional histological technique&#44;<a class="elsevierStyleCrossRef" href="#bib0210"><span class="elsevierStyleSup">14</span></a> or it was stored at &#8722;80<span class="elsevierStyleHsp" style=""></span>&#176;C for the RT-qPCR assays&#46; For the latter&#44; the total RNA of each sample was extracted with TRIzol&#44; transcribed into cDNA&#44; and 10<span class="elsevierStyleHsp" style=""></span>ng were amplified with TaqMan probes for &#946;-actin or by SYBR Green Master Mix &#40;Life Technologies&#44; Waltham&#44; MA&#44; United States&#41; with designed primers using the PubMed database&#58; TGF-&#946;1&#44; 5&#8242;-TTGCTTCAGCTCCACAGAGA-3&#8242; &#40;forward&#41; and 5&#8242;-TGGTTGTAGAGGGCAAGGAC-3&#8242; &#40;reverse&#41;&#59; fibronectin&#44; 5&#8242;-TGAGCGCCCTAAAGATTCCA-3&#8242; &#40;forward&#41; and 5&#8242;-TAGCCACCAGTCTCATGTGC-3&#8242; &#40;reverse&#41;&#59; collagen type I&#44; 5&#8242;-TCCTGGCAACAAAGGAGACA-3&#8242; &#40;forward&#41; and 5&#8242;-GGGCTCCTGGTTTTCCTTCT-3&#8242; &#40;reverse&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0210"><span class="elsevierStyleSup">14</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">The plasma and urinary chemistries&#44; creatinine and the plasma urea nitrogen&#44; were measured using commercial kits&#44; according to the manufacturer&#39;s instructions &#40;Arbor Assays LLC&#44; Ann Arbor&#44; MI&#44; United States&#41;&#46; The values of plasma and urinary concentration of the sodium ion &#40;Sodium Assay Kit&#44; Abcam&#44; Cambridge&#44; United Kingdom&#41; were used to calculate the fractional excretion of sodium&#46; The spectrophotometric determinations were carried out with the Victor Multimode Plate Reader Victor X4 &#40;PerkinElmer&#44; Waltham&#44; MA&#44; United States&#41;&#46;</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0090">Incubation with uremic toxins&#46; Parameters measured</span><p id="par0030" class="elsevierStylePara elsevierViewall">The HAOSMC were obtained by enzymatic dissociation of the aorta from 5 organ donors&#44; in accordance with the Spanish legal provisions&#44; with the approval of the Ethical Committee of the University Hospital of Getafe as previously described&#46;<a class="elsevierStyleCrossRef" href="#bib0215"><span class="elsevierStyleSup">15</span></a> These were generously donated by Dr&#46; S&#225;nchez-Ferrer&#46; The cells were maintained in DMEM culture medium supplemented with 10&#37; calf serum&#44; <span class="elsevierStyleSmallCaps">l</span>-glutamine&#44; amphotericin&#44; penicillin and streptomycin&#46; For the experiments&#44; the HAOSMC&#44; passages 3&#8211;10&#44; were cultured with 2&#46;5&#37; human serum &#40;AB serum&#59; BioWhittaker&#44; Walkersville&#44; MD&#44; United States&#41; for 24<span class="elsevierStyleHsp" style=""></span>h and incubated with the uremic solutes p-cresol &#40;pc&#41; and IS &#40;Sigma&#41;&#44; at concentrations of the uremic range &#40;IS&#58; 25 and 100<span class="elsevierStyleHsp" style=""></span>&#956;g&#47;ml and pc 10 and 100<span class="elsevierStyleHsp" style=""></span>&#956;g&#47;ml&#41;&#44; alone or combined together at low or high concentrations during a variable period of time&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">Once the treatments were finished&#44; the cell protein content was quantified by conventional Western blot<a class="elsevierStyleCrossRef" href="#bib0220"><span class="elsevierStyleSup">16</span></a> using primary antibodies against TGF-&#946;1&#44; collagen I or fibronectin &#40;Cell Signaling Technology&#44; Danvers&#44; MA&#44; United States&#41;&#46; The TGF-&#946;1 was also evaluated by immunofluorescence using confocal microscopy &#40;Leica17&#41;&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0095">Statistic analysis</span><p id="par0040" class="elsevierStylePara elsevierViewall">All the data was analyzed with the GraphPad Prism software&#46; The results are expressed as the mean<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>SEM&#46; As the number of animals or experiments was never greater than 10&#44; the comparisons were made for nonparametric data&#44; applying the Kruskal&#8211;Wallis test with Mann&#8211;Whitney post-test &#40;unpaired data&#41; or the Friedman test with Wilcoxon post test &#40;paired data&#41;&#46; A <span class="elsevierStyleItalic">p</span> value &#60;0&#46;05 was considered significant&#46;</p></span></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0100">Results</span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0105">Mice feed an adenine rich diet simultaneously develop chronic kidney disease and vascular damage&#46;</span><p id="par0045" class="elsevierStylePara elsevierViewall">In the mice experiments&#44; progressive CKD was generated by feeding the animals an adenine rich diet and the measurements were obtained at 2&#44; 4 or 6 weeks&#46; First&#44; the generation of CKD was illustrated by the change in parameters that are presented in <a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>&#46; Animals fed adenine rich diet exhibited a progressive increase in plasma creatinine and urea nitrogen concentrations&#44; as well as alterations in the handling of sodium and water&#44; manifested by the increase in diuresis and in the fractional excretion of sodium&#46; These changes were significant at 2 weeks and progressively worsens with the prolongation of the adenine administration &#40;<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>&#41;&#46; Next&#44; the possible vascular abnormalities were evaluated&#46; The changes in the vascular structure of the aortas that could be produced by progressive CKD were investigated by microscopic examination&#46; Mice with CKD induced by 6 weeks of adenine rich diet presented a thickening of the media layer and a moderate decrease of the radius of lummen &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 1</a>&#41;&#46; The morphometric analysis indicated that the thickness of the media is significantly higher in animals on Adenine than Controls&#46; In these two groups&#44; the radius of the lumen was not significantly different although it tends to be reduced in animals on adenine rich diet&#46; Therefore&#44; in these mice there was significant increase in the ratio media&#47;radius of lummen&#46; In addition&#44; uremic animals showed a progressive increase in the expression of the profibrotic cytokine TGF-&#946;1&#44; as well as the ECM proteins collagen type I and fibronectin&#44; tissue fibrosis markers as determined by RT-qPCR of the mice aortas &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 2</a>A and C&#41;&#44; which was significant for the 3 time periods in the case of TGF-&#946;1 and from week 4 for the ECM proteins&#46;</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0110">In cultured human aortic smooth muscle cells &#40;HAOSMC&#41; uremic toxins induce the expression of the profibrotic cytokine TGF-&#946;1 and extracellular matrix protein</span><p id="par0050" class="elsevierStylePara elsevierViewall">In vitro tests were performed using HAOSMC cells aiming to identify the mechanisms whereby uremic rats developed thickening of the aorta&#39;s wall&#46; We use a model developed in our laboratory that simulate in part the environment of uremia in moderate or advanced CKD by adding low&#44; high doses or mixtures of 2 uremic toxins &#40;IS and pc&#41; to the culture medium&#46; First&#44; cell viability assessed by MTT assays&#44; was demonstrated while on treatment with uremic toxins&#44; at the doses and times used&#44; by means of &#40;data not shown&#41;&#46; Second&#44; it was observed that uremic toxins induce a time and dose-dependent increase in TGF-&#946;1 expression&#44; after incubation with high doses&#44; of one or the two uremic toxins combined&#44; as determined by Western blot and immunofluorescence &#40;<a class="elsevierStyleCrossRef" href="#fig0020">Fig&#46; 3</a>A&#44; B&#41;&#46; The increase in TGF-&#946;1 expression was significant at 4<span class="elsevierStyleHsp" style=""></span>h of treatment&#46; The effect of both uremic toxins on TGF-&#946;1 expression is additive&#44; since the incubation with high doses of the two compounds simultaneously produces a significantly further increase in TGF-&#946;1 expression as compared with the separate treatment with each of the toxins &#40;Supplementary Fig&#46; 1A&#41;&#46; On the other hand&#44; the incubation with the toxins at low doses&#44; whether used separately or simultaneously&#44; does not induce changes in the expression of this cytokine &#40;data not shown&#41;&#46; In parallel&#44; the incubation with the high concentration of uremic toxins produced an increase in the expression of the ECN proteins&#44; collagen I and fibronectin&#44; that is significant at 2 and 4<span class="elsevierStyleHsp" style=""></span>h of treatment&#44; respectively &#40;<a class="elsevierStyleCrossRef" href="#fig0020">Fig&#46; 3</a>C and D&#41;&#46; Once again&#44; the effect is greater if the toxins are used in combination &#40;Supplementary Fig&#46; 1B and C&#41;&#46;</p><elsevierMultimedia ident="fig0020"></elsevierMultimedia></span></span><span id="sec0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0115">Discussion</span><p id="par0055" class="elsevierStylePara elsevierViewall">The main findings of this study are that uremia induces the expression of the profibrotic cytokine TGF-&#946;1 with the accumulation of ECM proteins in the aortas of mice with progressive uremia induced by adenine rich diet&#46; Also&#44; we show that uremic toxins induce the expression of these proteins in cultured HAOSMC cells&#46;</p><p id="par0060" class="elsevierStylePara elsevierViewall">Although there have been numerous studies aiming to identify CKD factors that could produce cardiovascular diseases&#44; there are few studies analyzing pathophysiological mechanisms whereby uremia induces accumulation of ECM proteins in the wall of large vessels leading cardiovascular damage in CKD patients&#46; Several studies have demonstrated the contribution of uremic toxins to vascular dysfunction&#44; but often the mechanisms involved are not clear&#46; It has been shown that IS stimulates the proliferation of VSMC through the production of reactive oxygen species&#44;<a class="elsevierStyleCrossRefs" href="#bib0195"><span class="elsevierStyleSup">11&#44;18</span></a> and it has been observed that the administration of this toxin promotes calcification and thickening of the aortic wall in hypertensive rats&#46;<a class="elsevierStyleCrossRef" href="#bib0235"><span class="elsevierStyleSup">19</span></a> In CKD patients&#44; vascular calcifications are observed particularly in the media&#44; also in the elastic fibers and surrounding the VSMC&#46;<a class="elsevierStyleCrossRef" href="#bib0240"><span class="elsevierStyleSup">20</span></a> It has been observed that the deposition of matrix in the artery wall my result from an active cellular process that involves the transdifferentiation of the VSMC into a cell type similar to the osteoblasts&#44; which leads to the deposit of ECM of osteogenic type&#44; a process that also it is induced by IS in vitro&#46;<a class="elsevierStyleCrossRef" href="#bib0245"><span class="elsevierStyleSup">21</span></a> Additionally&#44; both IS and p-CS induce cell dedifferentiation and renal fibrosis&#44; via epithelial&#8211;mesenchymal transition&#44; both in vitro and in vivo&#46;<a class="elsevierStyleCrossRefs" href="#bib0250"><span class="elsevierStyleSup">22&#44;23</span></a> However&#44; as far as we know&#44; the present work is the first that directly relates these uremic toxins with the increased production of profibrotic cytokines and fibrillar type ECM by HAOSMC&#46;</p><p id="par0065" class="elsevierStylePara elsevierViewall">Multiple studies have shown the importance of TGF-&#946;1 in the progression of CKD&#46;<a class="elsevierStyleCrossRef" href="#bib0260"><span class="elsevierStyleSup">24</span></a> Our research group has been interested for years in the study of the mechanisms responsible for the development and progression of tissue damage in cardiovascular and renal diseases&#46; The conceptual approach to the study of these mechanisms has been carried out from different perspectives&#44; but one of the possibilities is that the accumulation of ECM proteins&#44; at renal or vascular level&#44; may condition a positive feedback&#44; which leads to a worsening of the situation or a greater tissue damage&#46; We have reported that the contact of renal mesangial cells with abnormal collagens induces the synthesis of TGF-&#946;1<a class="elsevierStyleCrossRef" href="#bib0265"><span class="elsevierStyleSup">25</span></a> and the production of TGF-&#946;1 is also stimulated by free radicals&#44;<a class="elsevierStyleCrossRef" href="#bib0225"><span class="elsevierStyleSup">17</span></a> and that in both cases&#44; the fibrotic process self-perpetuates&#44; increasing the expression of ECM proteins&#44; such as collagen I and IV and fibronectin&#44;<a class="elsevierStyleCrossRefs" href="#bib0225"><span class="elsevierStyleSup">17&#44;25</span></a> which favor the progression of CKD&#46; In the resent study we have shown a direct relationship between solutes that accumulate in the serum of uremic patients such as protein bound uremic toxins&#44; IS and pc&#44; and the production of TGF-&#946;1 and MEC by HAOSMC&#46; It is possible that the origin of this phenomenon is the increase of reactive oxygen species induced by uremic toxins&#44; a phenomenon described in vascular endothelial cells by others and ourselves&#44;<a class="elsevierStyleCrossRefs" href="#bib0180"><span class="elsevierStyleSup">8&#44;16</span></a> in monocytes and macrophages&#44;<a class="elsevierStyleCrossRef" href="#bib0180"><span class="elsevierStyleSup">8</span></a> in renal tubule cells<a class="elsevierStyleCrossRef" href="#bib0240"><span class="elsevierStyleSup">20</span></a> and in rat VSMC&#44;<a class="elsevierStyleCrossRef" href="#bib0230"><span class="elsevierStyleSup">18</span></a> and that we have verified in the in vitro uremia model used in this work &#40;data not shown&#41;&#46;</p><p id="par0070" class="elsevierStylePara elsevierViewall">In addition&#44; we have explored the additive effect of the two toxins&#44; IS and pc&#44; as previously observed when p-CS is combined with para-cresyl glucuronide&#46;<a class="elsevierStyleCrossRef" href="#bib0270"><span class="elsevierStyleSup">26</span></a> A possible limitation in the clinical translation of any of our results is the use of the PC acting as a substitute for p-CS&#44; a PC derivative by sulfation which is its main circulating metabolite&#46; PC was for a long time considered one of the main uremic toxins&#44; but it is currently known to circulate freely in plasma in very low amounts&#44; and that the main cresols that are actually retained in uremia are p-CS and para-cresil glucuronide&#44; the other conjugate of pc&#46;<a class="elsevierStyleCrossRef" href="#bib0275"><span class="elsevierStyleSup">27</span></a> We have used a rat model of uremia in which animals are maintained on a diet containing high amounts of Adenine which causes nephrotoxicity when metabolized to 2&#44;8-dihydroxyadenine&#44; an insoluble compound that precipitates in the renal tubules as crystals&#44; producing tubule occlusion&#44; inflammation and tubuloinsterstitial fibrosis&#46;<a class="elsevierStyleCrossRef" href="#bib0205"><span class="elsevierStyleSup">13</span></a> Since functional and structural alterations are similar to those observed in CKD and occur gradually and progressively&#44; this model has been very useful to examine the pathophysiological mechanisms that cause cardiovascular disease in CKD&#46; In fact&#44; in the aortas of these animals we have observed a thickening of the media&#44; which is also observed in coronary arteries of uremic patients&#44; as well as the thickening of the intima-media of carotid arteries&#46;<a class="elsevierStyleCrossRef" href="#bib0180"><span class="elsevierStyleSup">8</span></a> In addition&#44; we found a progressive accumulation of ECM proteins in the aortic wall&#44; a process that has been related&#44; together with the decrease in elastin levels&#44; with the arterial remodeling characterized by stiffness of the aorta and the major arteries&#44; whose main pathophysiological consequence is the loss of arterial distensibility&#46;<a class="elsevierStyleCrossRef" href="#bib0180"><span class="elsevierStyleSup">8</span></a></p><p id="par0075" class="elsevierStylePara elsevierViewall">Finally&#44; the concentrations of toxins that we use in this study are within the range reported in uremic patients &#40;1&#8211;100<span class="elsevierStyleHsp" style=""></span>&#956;g&#47;ml&#41;&#44;<a class="elsevierStyleCrossRef" href="#bib0280"><span class="elsevierStyleSup">28</span></a> but in uremic patients the values of these uremic toxins could be has high as 236 and 105<span class="elsevierStyleHsp" style=""></span>&#956;g&#47;ml for the IS and p-CS respectively&#44; in hemodialysis patients&#44;<a class="elsevierStyleCrossRef" href="#bib0280"><span class="elsevierStyleSup">28</span></a> and less than 4&#46;9 and 46<span class="elsevierStyleHsp" style=""></span>&#956;g&#47;ml for IS and p-CS respectively&#44; in patients with CKD not on dialysis&#44; for whom there is very scarce information&#46;<a class="elsevierStyleCrossRef" href="#bib0220"><span class="elsevierStyleSup">16</span></a> In addition&#44; higher levels of both toxins have been observed in patients with CKD stages 1&#8211;5 that are progressor vs&#46; the non progressors&#46;<a class="elsevierStyleCrossRef" href="#bib0220"><span class="elsevierStyleSup">16</span></a> Results from in vitro and in vivo experiments&#44; indicate that there is a significant increase in the production and&#47;or accumulation of ECM proteins when exposed to high concentration the uremic toxins&#44; or after 4 weeks of high adenine diet&#46;</p></span><span id="sec0050" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0120">Conclusion</span><p id="par0080" class="elsevierStylePara elsevierViewall">The present work demonstrates for the first time that uremic toxins that accumulate in patients with end stage kidney diseases induce the expression of the cytokine TGF-&#946;1 and proteins of ECM by the HAOSMC&#46; This could explain the mechanism of vascular damage and ECM accumulation observed in vivo in the model of progressive CKD induced by adenine rich diet&#46;</p></span><span id="sec0055" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0125">Financing</span><p id="par0085" class="elsevierStylePara elsevierViewall">This work has been financed by the <span class="elsevierStyleGrantSponsor" id="gs1">Carlos III Health Institute &#40;ISCIII&#41;</span> and <span class="elsevierStyleGrantSponsor" id="gs2">FEDER</span> funds &#40;<span class="elsevierStyleGrantNumber" refid="gs2">PI14&#47;02075</span>&#44; <span class="elsevierStyleGrantNumber" refid="gs2">PI17&#47;00625</span>&#44; <span class="elsevierStyleGrantNumber" refid="gs2">PI17&#47;01513</span>&#41;&#44; <span class="elsevierStyleGrantSponsor" id="gs3">FEDER funds and ISCIII RETIC REDinREN</span> programs &#40;<span class="elsevierStyleGrantNumber" refid="gs3">RD12&#47;0021&#47;0006</span> and <span class="elsevierStyleGrantNumber" refid="gs3">RD16&#47;0009&#47;0018</span>&#41;&#44; <span class="elsevierStyleGrantSponsor" id="gs4">Autonomous Community of Madrid</span> &#40;NOVELREN-CM REF&#58; <span class="elsevierStyleGrantNumber" refid="gs4">B2017&#47;BMD-3751</span>&#41;&#44; <span class="elsevierStyleGrantSponsor" id="gs5">University of Alcal&#225;</span> &#40;<span class="elsevierStyleGrantNumber" refid="gs5">CCG2016&#47;BIO-043</span>&#41; and the <span class="elsevierStyleGrantSponsor" id="gs6">Senefro Foundation</span> &#40;Senefro-2016&#41; to LCB&#44; and <span class="elsevierStyleGrantSponsor" id="gs7">Renal Foundation I&#241;igo &#193;lvarez de Toledo &#40;FRIAT&#41;</span>&#46;</p></span><span id="sec0060" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0130">Authorship</span><p id="par0090" class="elsevierStylePara elsevierViewall">Diego Rodr&#237;guez-Puyol and Laura Calleros share the direction of this work&#46;</p></span><span id="sec0065" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0135">Conflicts of interest</span><p id="par0095" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest&#46;</p></span></span>"
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      "en" => array:3 [
        "titulo" => "Abstract"
        "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Background</span><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Patients with chronic kidney disease present with an accumulation of uremic toxins&#44; which have been identified as pathogenic agents associated with cardiovascular mortality&#44; which is very high is this patient group&#46; A phenomenon common to the progressive renal dysfunction and associated vascular damage&#44; is the abnormal accumulation of extracellular matrix &#40;ECM&#41; proteins in the renal or vascular structures&#46;</p></span> <span id="abst0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Objective</span><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">To determine the contribution of uremia or the uremic toxins to the production of cytokinins and ECM in aortas of uremic animals or human aortic smooth muscle cells &#40;HASMCs&#41;&#46;</p></span> <span id="abst0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Materials and methods</span><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Mice were used with uremia induced by a diet rich in adenine &#40;0&#46;2&#37;&#41; for 2&#44; 4 or 6 weeks&#46; Kidney function was evaluated by means of urine volume&#44; plasma levels of creatinine&#44; urea&#44; fractional excretion of sodium&#44; and vascular damage using histology&#44; as well as protein expression using RT-qPCR&#46; The HASMCs were incubated in vitro with uremic toxins&#58; p-cresol 10&#8211;100 &#40;&#956;g&#47;ml&#41; and indoxyl-sulphate 25&#8211;100 &#40;&#956;g&#47;ml&#41; alone or simultaneously&#46; The protein expression was evaluated using Western blot and confocal microscopy&#46;</p></span> <span id="abst0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Results</span><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">The administration of adenine produced progressive kidney damage in the mice&#44; thickening of the aortic wall&#44; and increasing the expression of TGF-&#946;1 and ECM proteins&#46; The toxins at high doses and combined also induced the expression of TGF-&#946;1 and ECM proteins by the HASMCs&#46;</p></span> <span id="abst0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Conclusions</span><p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">The uremia produced by an adenine rich diet or high doses of uremic toxins induced the abnormal deposit of ECM proteins in the vascular wall or its production by HASMCs&#46; The understanding of the mechanisms that underlie this pathophysiological process may be useful in the prevention of cardiovascular damage associated with the progress of chronic kidney disease&#44; a disease&#44; at the moment that is irreversible and occasional silent until its diagnosis in advanced stages&#46;</p></span>"
        "secciones" => array:5 [
          0 => array:2 [
            "identificador" => "abst0005"
            "titulo" => "Background"
          ]
          1 => array:2 [
            "identificador" => "abst0010"
            "titulo" => "Objective"
          ]
          2 => array:2 [
            "identificador" => "abst0015"
            "titulo" => "Materials and methods"
          ]
          3 => array:2 [
            "identificador" => "abst0020"
            "titulo" => "Results"
          ]
          4 => array:2 [
            "identificador" => "abst0025"
            "titulo" => "Conclusions"
          ]
        ]
      ]
      "es" => array:3 [
        "titulo" => "Resumen"
        "resumen" => "<span id="abst0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">Antecedentes</span><p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">Los pacientes con enfermedad renal cr&#243;nica presentan una acumulaci&#243;n de toxinas ur&#233;micas&#44; las cuales han sido identificadas como agentes patog&#233;nicos asociados con la mortalidad cardiovascular&#44; muy elevada en este grupo de enfermos&#46; Un fen&#243;meno com&#250;n a la disfunci&#243;n renal progresiva y al da&#241;o vascular asociado es la acumulaci&#243;n anormal de prote&#237;nas de la matriz extracelular &#40;MEC&#41; en las estructuras renales o vasculares&#46;</p></span> <span id="abst0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">Objetivo</span><p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">Estudiar la contribuci&#243;n de la uremia o las toxinas ur&#233;micas a la producci&#243;n de citocinas y MEC en aortas de animales ur&#233;micos o c&#233;lulas de m&#250;sculo liso de aorta humana &#40;HAOSMC&#41;&#46;</p></span> <span id="abst0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0050">Materiales y m&#233;todos</span><p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">Se utilizaron ratones con uremia inducida por una dieta rica en adenina &#40;0&#44;2&#37;&#41; durante 2&#44; 4 o 6 semanas&#46; Se evalu&#243; la funci&#243;n renal mediante la diuresis&#44; los niveles plasm&#225;ticos de creatinina y nitr&#243;geno ureico plasm&#225;tico&#44; y la excreci&#243;n fraccional de sodio y el da&#241;o vascular mediante histolog&#237;a y expresi&#243;n proteica por RT-qPCR&#46; <span class="elsevierStyleItalic">In vitro</span>&#44; las HAOSMC se incubaron con toxinas ur&#233;micas&#58; p-cresol 10-100 &#40;&#956;g&#47;ml&#41; e indoxil-sulfato 25-100 &#40;&#956;g&#47;ml&#41;&#44; solas o simult&#225;neamente&#46; La expresi&#243;n proteica se evalu&#243; por Western blot y microscopia confocal&#46;</p></span> <span id="abst0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0055">Resultados</span><p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">La administraci&#243;n de adenina produjo un progresivo da&#241;o renal en los ratones&#44; un engrosamiento de la pared a&#243;rtica y un incremento de la expresi&#243;n de TGF-&#946;1 y prote&#237;nas de MEC&#46; Las toxinas a dosis altas y combinadas tambi&#233;n indujeron expresi&#243;n de TGF-&#946;1 y prote&#237;nas de MEC por las c&#233;lulas HAOSMC&#46;</p></span> <span id="abst0050" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0060">Conclusiones</span><p id="spar0050" class="elsevierStyleSimplePara elsevierViewall">La uremia producida por una dieta rica en adenina o las dosis altas de toxinas ur&#233;micas indujeron el dep&#243;sito anormal de prote&#237;nas de MEC en las paredes vasculares o su producci&#243;n por HAOSMC&#46; La comprensi&#243;n de los mecanismos que subyacen a este proceso fisiopatol&#243;gico puede resultar de utilidad en la prevenci&#243;n del da&#241;o cardiovascular asociado a la progresi&#243;n de la enfermedad renal cr&#243;nica&#44; una dolencia&#44; de momento&#44; irreversible y&#44; en ocasiones&#44; silenciosa hasta su diagn&#243;stico en etapas avanzadas&#46;</p></span>"
        "secciones" => array:5 [
          0 => array:2 [
            "identificador" => "abst0030"
            "titulo" => "Antecedentes"
          ]
          1 => array:2 [
            "identificador" => "abst0035"
            "titulo" => "Objetivo"
          ]
          2 => array:2 [
            "identificador" => "abst0040"
            "titulo" => "Materiales y m&#233;todos"
          ]
          3 => array:2 [
            "identificador" => "abst0045"
            "titulo" => "Resultados"
          ]
          4 => array:2 [
            "identificador" => "abst0050"
            "titulo" => "Conclusiones"
          ]
        ]
      ]
    ]
    "NotaPie" => array:1 [
      0 => array:2 [
        "etiqueta" => "&#9734;"
        "nota" => "<p class="elsevierStyleNotepara" id="npar0015">Please cite this article as&#58; Hatem-Vaquero M&#44; de Frutos S&#44; Luengo A&#44; Gonz&#225;lez Abajo A&#44; Griera M&#44; Rodr&#237;guez-Puyol M&#44; et al&#46; Contribuci&#243;n de las toxinas ur&#233;micas a la fibrosis vascular asociada a la enfermedad renal cr&#243;nica&#46; Nefrologia&#46; 2018&#59;38&#58;639&#8211;646&#46;</p>"
      ]
    ]
    "apendice" => array:1 [
      0 => array:1 [
        "seccion" => array:1 [
          0 => array:4 [
            "apendice" => "<p id="par0105" class="elsevierStylePara elsevierViewall">The following are the supplementary data to this article&#58;<elsevierMultimedia ident="fig0005"></elsevierMultimedia></p>"
            "etiqueta" => "Appendix A"
            "titulo" => "Supplementary data"
            "identificador" => "sec0075"
          ]
        ]
      ]
    ]
    "multimedia" => array:5 [
      0 => array:7 [
        "identificador" => "fig0010"
        "etiqueta" => "Fig&#46; 1"
        "tipo" => "MULTIMEDIAFIGURA"
        "mostrarFloat" => true
        "mostrarDisplay" => false
        "figura" => array:1 [
          0 => array:4 [
            "imagen" => "gr1.jpeg"
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        "descripcion" => array:1 [
          "en" => "<p id="spar0055" class="elsevierStyleSimplePara elsevierViewall">Mice with CKD induced by adenine-rich diet develop vascular structural damage&#46; Mice were fed standard diet &#40;Control&#41; or rich in adenine &#40;adenine&#41; during 6 weeks&#46; &#40;A&#41; The aortas were stained with hematoxylin-eosin&#46; Representative changes are shown&#46; In Control mice&#44; no lesions are seen&#46; Note the thickening of the media &#40;asterisk&#41; of the aortas of the mice fed with Adenine&#46; Scale bar&#58; 100<span class="elsevierStyleHsp" style=""></span>&#956;m&#46; Magnification 20&#215;&#46; &#40;B&#41; Morphometric analysis of the thickness of the media and the radius of the lumen&#44; made by the ImageJ software and calculation of its ratio&#46; The mean of 5 independent measurements in different directions is considered mean radius&#46; The values are presented as the mean<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>SEM&#46; <span class="elsevierStyleSup">1</span><span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>0&#46;05 vs&#46; Control&#46; <span class="elsevierStyleItalic">n</span><span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>5 animals&#47;group&#46;</p>"
        ]
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      1 => array:7 [
        "identificador" => "fig0015"
        "etiqueta" => "Fig&#46; 2"
        "tipo" => "MULTIMEDIAFIGURA"
        "mostrarFloat" => true
        "mostrarDisplay" => false
        "figura" => array:1 [
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            "imagen" => "gr2.jpeg"
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        "descripcion" => array:1 [
          "en" => "<p id="spar0060" class="elsevierStyleSimplePara elsevierViewall">Mice with CKD induced by a adenine rich diet show the aorta with increased expression of the profibrotic cytokine TGF-&#946;1 and in the extracellular matrix genes&#46; The mice were fed for 2&#44; 4 or 6 weeks with either the standard diet &#40;Control&#44; black circles&#41; or with a diet rich in adenine &#40;Adenine&#44; black triangles&#41;&#46; The mRNA levels of TGF-&#946;1 &#40;A&#41;&#44; collagen I &#40;COL I&#44; B&#41; or fibronectin &#40;C&#41; in the aorta were determined by RT-qPCR&#46; The total &#946;-actin levels were as their respective endogenous controls&#46; The values are presented as the mean<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>SEM vs&#46; Control&#46; &#42; <span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>0&#46;05 vs&#46; 2 weeks&#44; <span class="elsevierStyleSup">1</span><span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>0&#46;05 vs&#46; Control&#44; at the same time period&#46; <span class="elsevierStyleItalic">n</span><span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>5 animals&#47;group&#46;</p>"
        ]
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        "identificador" => "fig0020"
        "etiqueta" => "Fig&#46; 3"
        "tipo" => "MULTIMEDIAFIGURA"
        "mostrarFloat" => true
        "mostrarDisplay" => false
        "figura" => array:1 [
          0 => array:4 [
            "imagen" => "gr3.jpeg"
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        "descripcion" => array:1 [
          "en" => "<p id="spar0065" class="elsevierStyleSimplePara elsevierViewall">High doses of uremic toxins induce the expression of the profibrotic cytokine TGF-&#946;1 and extracellular matrix proteins in vascular smooth muscle cells&#46; Human aortic smooth muscle cells were incubated with medium supplemented with 2&#46;5&#37; human serum for 24<span class="elsevierStyleHsp" style=""></span>h&#46; Subsequently they were treated for 2&#44; 4&#44; 6 or 24<span class="elsevierStyleHsp" style=""></span>h &#40;A&#44; C and D&#41; or 24<span class="elsevierStyleHsp" style=""></span>h &#40;B&#41; with uremic toxins&#58; indoxil-sulfate &#40;IS 100<span class="elsevierStyleHsp" style=""></span>&#956;g&#47;ml&#41;&#44; para-cresol &#40;pc 100<span class="elsevierStyleHsp" style=""></span>&#956;g&#47;ml&#41; or a mixture of both &#40;IS<span class="elsevierStyleHsp" style=""></span>&#43;<span class="elsevierStyleHsp" style=""></span>1pc 100<span class="elsevierStyleHsp" style=""></span>&#956;g&#47;ml&#41;&#46; Representative Western blots of TGF-&#946;1 &#40;A&#41;&#44; collagen I &#40;COL I&#44; C&#41; and fibronectin &#40;D&#41; are shwon&#46; The levels of GAPDH were determined as their respective endogenous controls&#46; The bars represent the values of the densitometric analysis of the normalized blots against the endogenous control&#46; The expression of TGF-&#946;1 was analyzed by immunofluorescence &#40;B&#41;&#46; Representative images of the photographs obtained by confocal microscopy &#40;100&#215;&#41; are shown&#46; The values are represented as the mean<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>SEM&#46; &#42; <span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>0&#46;05 vs&#46; Control &#40;CT&#44; untreated cells&#41;&#46;</p>"
        ]
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        "identificador" => "tbl0005"
        "etiqueta" => "Table 1"
        "tipo" => "MULTIMEDIATABLA"
        "mostrarFloat" => true
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        "detalles" => array:1 [
          0 => array:3 [
            "identificador" => "at1"
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        "tabla" => array:3 [
          "leyenda" => "<p id="spar0075" class="elsevierStyleSimplePara elsevierViewall">The mice were fed a standard diet &#40;Control&#41; or a diet rich in adenine &#40;adenine&#41;&#44; for 2&#44; 4&#44; or 6 weeks&#46; Renal function was assessed by measuring diuresis&#44; plasma creatinine&#44; plasma urea nitrogen levels&#44; and fractional excretion sodium&#46; The values are represented as the mean<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>SEM&#46;</p>"
          "tablatextoimagen" => array:1 [
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              "tabla" => array:1 [
                0 => """
                  <table border="0" frame="\n
                  \t\t\t\t\tvoid\n
                  \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><th class="td" title="table-head  " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">Parameters&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</th><th class="td" title="table-head  " align="center" valign="top" scope="col" style="border-bottom: 2px solid black">0 weeks&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</th><th class="td" title="table-head  " align="center" valign="top" scope="col" style="border-bottom: 2px solid black">2 weeks&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</th><th class="td" title="table-head  " align="center" valign="top" scope="col" style="border-bottom: 2px solid black">4 weeks&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</th><th class="td" title="table-head  " align="center" valign="top" scope="col" style="border-bottom: 2px solid black">6 weeks&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</th></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td" title="table-entry  " colspan="5" align="left" valign="top"><span class="elsevierStyleItalic">Diuresis &#40;&#956;l&#47;24</span><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">h&#41;</span></td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>Control&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">432<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>49&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">421<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>52&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">445<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>48&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">439<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>48&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>Adenine&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">431<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>56&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">3&#46;968<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>524<a class="elsevierStyleCrossRef" href="#tblfn0005"><span class="elsevierStyleSup">&#42;</span></a><span class="elsevierStyleSup">&#44;</span><a class="elsevierStyleCrossRef" href="#tblfn0010"><span class="elsevierStyleSup">&#42;&#42;</span></a>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">6&#46;382<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>615<a class="elsevierStyleCrossRef" href="#tblfn0005"><span class="elsevierStyleSup">&#42;</span></a><span class="elsevierStyleSup">&#44;</span><a class="elsevierStyleCrossRef" href="#tblfn0010"><span class="elsevierStyleSup">&#42;&#42;</span></a>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">6&#46;115<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>627<a class="elsevierStyleCrossRef" href="#tblfn0005"><span class="elsevierStyleSup">&#42;</span></a><span class="elsevierStyleSup">&#44;</span><a class="elsevierStyleCrossRef" href="#tblfn0010"><span class="elsevierStyleSup">&#42;&#42;</span></a>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry  " colspan="5" align="left" valign="top"><span class="elsevierStyleVsp" style="height:0.5px"></span></td></tr><tr title="table-row"><td class="td" title="table-entry  " colspan="5" align="left" valign="top"><span class="elsevierStyleItalic">Plasma creatinine &#40;mg&#47;dl&#41;</span></td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>Control&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">0&#46;28<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;07&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">0&#46;26<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;1&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">0&#46;31<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;06&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">0&#46;25<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;02&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>Adenine&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">0&#46;29<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;06&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">0&#46;63<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;13&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">0&#46;70<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;12<a class="elsevierStyleCrossRef" href="#tblfn0005"><span class="elsevierStyleSup">&#42;</span></a><span class="elsevierStyleSup">&#44;</span><a class="elsevierStyleCrossRef" href="#tblfn0010"><span class="elsevierStyleSup">&#42;&#42;</span></a>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">0&#46;86<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;07<a class="elsevierStyleCrossRef" href="#tblfn0005"><span class="elsevierStyleSup">&#42;</span></a><span class="elsevierStyleSup">&#44;</span><a class="elsevierStyleCrossRef" href="#tblfn0010"><span class="elsevierStyleSup">&#42;&#42;</span></a>&nbsp;\t\t\t\t\t\t\n
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Article information
ISSN: 20132514
Original language: English
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2021 March 55 34 89
2021 February 63 34 97
2021 January 29 26 55
2020 December 44 23 67
2020 November 33 22 55
2020 October 49 30 79
2020 September 48 22 70
2020 August 32 25 57
2020 July 41 11 52
2020 June 46 35 81
2020 May 55 16 71
2020 April 57 17 74
2020 March 115 31 146
2020 February 63 14 77
2020 January 75 37 112
2019 December 71 30 101
2019 November 106 22 128
2019 October 115 13 128
2019 September 101 27 128
2019 August 56 18 74
2019 July 65 32 97
2019 June 42 35 77
2019 May 159 28 187
2019 April 89 54 143
2019 March 56 39 95
2019 February 31 25 56
2019 January 40 49 89
2018 December 70 58 128
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¿Es usted profesional sanitario apto para prescribir o dispensar medicamentos?

Are you a health professional able to prescribe or dispense drugs?