Contribution of uraemic toxins to the vascular fibrosis associated with chronic kidney disease

被引:5
作者
Hatem-Vaquero, Marco [1 ,2 ,3 ,4 ]
de Frutos, Sergio [1 ,2 ,3 ,4 ]
Luengo, Alicia [1 ,2 ,3 ]
Abajo, Alba Gonzalez [2 ,3 ,4 ,5 ,6 ]
Griera, Mercedes [1 ,2 ,3 ,4 ]
Rodriguez-Puyol, Manuel [1 ,2 ,3 ]
Rodriguez-Puyol, Diego [2 ,3 ,4 ,5 ,6 ,7 ]
Calleros, Laura [1 ,2 ,3 ,4 ]
机构
[1] Univ Alcala, Dept Biol Sistemas, Madrid, Spain
[2] FRIAT, Madrid, Spain
[3] Inst Ramon y Cajal Invest Sanitaria IRYCIS, Madrid, Spain
[4] Inst Salud Carlos III, Red Invest Renal REDinREN, Madrid, Spain
[5] Hosp Univ Principe Asturias, Secc Nefrol, Madrid, Spain
[6] Hosp Univ Principe Asturias, Fdn Invest, Madrid, Spain
[7] Univ Alcala, Dept Med & Especialidades Med, Madrid, Spain
来源
NEFROLOGIA | 2018年 / 38卷 / 06期
关键词
Chronic kidney disease; Vascular damage; Uraemic toxins; Adenine Fibrosis; Transforming Growth factor; beta-1; OSTEOBLAST-SPECIFIC PROTEINS; CARDIOVASCULAR EVENTS; SULFATE; EXPRESSION; BETA; PROLIFERATION;
D O I
10.1016/j.nefro.2018.07.008
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: Patients with chronic kidney disease present with an accumulation of uraemic toxins, which have been identified as pathogenic agents associated with cardiovascular mortality, which is very high is this patient group. A phenomenon common to the progressive renal dysfunction and associated vascular damage, is the abnormal accumulation of extracellular matrix (ECM) proteins in the renal or vascular structures. Objective: To determine the contribution of uraemia or the uraemic toxins to the production of cytokinins and ECM in aortas of uraemic animals or human aortic smooth muscle cells (HASMCs). Materials and methods: Mice were used with uraemia induced by a diet rich in adenine (0.2%) for 2, 4 or 6 weeks. Kidney function was evaluated by means of urine volume, plasma levels of creatinine, urea, fractional excretion of sodium, and vascular damage using histology, as well as protein expression using RT-qPCR. The HASMCs were incubated in vitro with uraemic toxins: p-cresol 10-100 (mu g/ml) and indoxyl-sulphate25-100 (mu g/ml) alone or simultaneously. The protein expression was evaluated using Western blot and confocal microscopy. Results: The administration of adenine produced progressive kidney damage in the mice, thickening of the aortic wall, and increasing the expression of TGF-beta 1 and ECM proteins. The toxins at high doses and combined also induced the expression of TGF-beta 1 and ECM proteins by the HASMCs. Conclusions: The uraemia produced by an adenine rich diet or high doses of uraemic toxins induced the abnormal deposit of ECM proteins in the vascular wall or its production by HASMCs. 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, a disease, at the moment that is irreversible and occasional silent until its diagnosis in advanced stages. (C) 2018 Sociedad Espanola de Nefrologia. Published by Elsevier Espana, S.L.U. This is an open access article under the CC BY-NC-ND license
引用
收藏
页码:639 / 646
页数:8
相关论文
共 28 条
[1]   Indoxyl sulphate promotes aortic calcification with expression of osteoblast-specific proteins in hypertensive rats [J].
Adijiang, Ayinuer ;
Goto, Sumie ;
Uramoto, Satsuki ;
Nishijima, Fuyuhiko ;
Niwa, Toshimitsu .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2008, 23 (06) :1892-1901
[2]   Free serum concentrations of the protein-bound retention solute p-cresol predict mortality in hemodialysis patients [J].
Bammens, B ;
Evenepoel, P ;
Keuleers, H ;
Verbeke, K ;
Vanrenterghem, Y .
KIDNEY INTERNATIONAL, 2006, 69 (06) :1081-1087
[3]   Serum Indoxyl Sulfate Is Associated with Vascular Disease and Mortality in Chronic Kidney Disease Patients [J].
Barreto, Fellype C. ;
Barreto, Daniela V. ;
Liabeuf, Sophie ;
Meert, Natalie ;
Glorieux, Griet ;
Temmar, Mohammed ;
Choukroun, Gabriel ;
Vanholder, Raymond ;
Massy, Ziad A. .
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2009, 4 (10) :1551-1558
[4]   Prevalence of subclinical atheromatosis and associated risk factors in chronic kidney disease: the NEFRONA study [J].
Betriu, Angels ;
Martinez-Alonso, Montserrat ;
Vittoria Arcidiacono, Maria ;
Cannata-Andia, Jorge ;
Pascual, Julio ;
Manuel Valdivielso, Jose ;
Fernandez, Elvira .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2014, 29 (07) :1415-1422
[5]   Indoxyl Sulfate Induces Epithelial-to-Mesenchymal Transition in Rat Kidneys and Human Proximal Tubular Cells [J].
Bolati, Dilinaer ;
Shimizu, Hidehisa ;
Higashiyama, Yukihiro ;
Nishijima, Fuyuhiko ;
Niwa, Toshimitsu .
AMERICAN JOURNAL OF NEPHROLOGY, 2011, 34 (04) :318-323
[6]   Does Uremia Cause Vascular Dysfunction? [J].
Brunet, Philippe ;
Gondouin, Bertrand ;
Duval-Sabatier, Ariane ;
Dou, Laetitia ;
Cerini, Claire ;
Dignat-George, Francoise ;
Jourde-Chiche, Noemie ;
Argiles, Angel ;
Burtey, Stephane .
KIDNEY & BLOOD PRESSURE RESEARCH, 2011, 34 (04) :284-290
[7]   The apolipoprotein E knockout mouse:: A model documenting accelerated atherogenesis in uremia [J].
Buzello, M ;
Törnig, J ;
Faulhaber, J ;
Ehmke, H ;
Ritz, E ;
Amann, K .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2003, 14 (02) :311-316
[8]   Urea-induced ROS generation causes insulin resistance in mice with chronic renal failure [J].
D'Apolito, Maria ;
Du, Xueliang ;
Zong, Haihong ;
Catucci, Alessandra ;
Maiuri, Luigi ;
Trivisano, Tiziana ;
Pettoello-Mantovani, Massimo ;
Campanozzi, Angelo ;
Raia, Valeria ;
Pessin, Jeffrey E. ;
Brownlee, Michael ;
Giardino, Ida .
JOURNAL OF CLINICAL INVESTIGATION, 2010, 120 (01) :203-213
[9]   Normal and Pathologic Concentrations of Uremic Toxins [J].
Duranton, Flore ;
Cohen, Gerald ;
De Smet, Rita ;
Rodriguez, Mariano ;
Jankowski, Joachim ;
Vanholder, Raymond ;
Argiles, Angel .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2012, 23 (07) :1258-1270
[10]  
Foley RN, 1998, J AM SOC NEPHROL, V9, P267