Beyond proteinuria: VDR activation reduces renal inflammation in experimental diabetic nephropathy

被引:141
作者
Sanchez-Nino, Maria-Dolores [4 ,5 ]
Bozic, Milica [2 ]
Cordoba-Lanus, Elizabeth [6 ,7 ]
Valcheva, Petya [2 ]
Gracia, Olga [2 ]
Ibarz, Merce [3 ]
Fernandez, Elvira [2 ]
Navarro-Gonzalez, Juan F. [6 ,7 ]
Ortiz, Alberto [4 ,5 ]
Manuel Valdivielso, Jose [1 ,2 ]
机构
[1] Hosp Arnau Vilanova, Lab Invest, IRBLLEIDA, Dept Nephrol, Lleida 25198, Spain
[2] Hosp Arnau Vilanova, IRBLLEIDA, Res Lab, Lleida 25198, Spain
[3] Hosp Arnau Vilanova, IRBLLEIDA, Dept Biochem, Lleida 25198, Spain
[4] Univ Autonoma Madrid, IIS Fdn Jimenez Diaz, Madrid, Spain
[5] Inst Reina Sofia Invest Nefrol IRSIN, Madrid, Spain
[6] Hosp Univ Nuestra Senora Candelaria, Serv Nefrol, Santa Cruz De Tenerife, Spain
[7] Hosp Univ Nuestra Senora Candelaria, Unidad Invest, Santa Cruz De Tenerife, Spain
关键词
glomerular disease; interleukins; microalbuminuria; NF-KAPPA-B; VITAMIN-D-RECEPTOR; RENIN-ANGIOTENSIN SYSTEM; 1,25-DIHYDROXYVITAMIN D-3; D ANALOG; COMBINATION THERAPY; KIDNEY-DISEASE; SUPPRESSES; EXPRESSION; CELLS;
D O I
10.1152/ajprenal.00090.2011
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Sanchez-Nino M, Bozic M, Cordoba-Lanus E, Valcheva P, Gracia O, Ibarz M, Fernandez E, Navarro-Gonzalez JF, Ortiz A, Valdivielso JM. Beyond proteinuria: VDR activation reduces renal inflammation in experimental diabetic nephropathy. Am J Physiol Renal Physiol 302: F647-F657, 2012. First published December 14, 2011; doi:10.1152/ajprenal.00090.2011.-Local inflammation is thought to contribute to the progression of diabetic nephropathy. The vitamin D receptor (VDR) activator paricalcitol has an antiproteinuric effect in human diabetic nephropathy at high doses. We have explored potential anti-inflammatory effects of VDR activator doses that do not modulate proteinuria in an experimental model of diabetic nephropathy to gain insights into potential benefits of VDR activators in those patients whose proteinuria is not decreased by this therapy. The effect of calcitriol and paricalcitol on renal function, albuminuria, and renal inflammation was explored in a rat experimental model of diabetes induced by streptozotocin. Modulation of the expression of mediators of inflammation by these drugs was explored in cultured podocytes. At the doses used, neither calcitriol nor paricalcitol significantly modified renal function or reduced albuminuria in experimental diabetes. However, both drugs reduced the total kidney mRNA expression of IL-6, monocyte chemoattractant protein (MCP)-1, and IL-18. Immunohistochemistry showed that calcitriol and paricalcitol reduced MCP-1 and IL-6 in podocytes and tubular cells as well as glomerular infiltration by macrophages, glomerular cell NF-kappa B activation, apoptosis, and extracellular matrix deposition. In cultured podocytes, paricalcitol and calcitriol at concentrations in the physiological and clinically significant range prevented the increase in MCP-1, IL-6, renin, and fibronectin mRNA expression and the secretion of MCP-1 to the culture media induced by high glucose. In conclusion, in experimental diabetic nephropathy VDR activation has local renal anti-inflammatory effects that can be observed even when proteinuria is not decreased. This may be ascribed to decreased inflammatory responses of intrinsic renal cells, including podocytes, to high glucose.
引用
收藏
页码:F647 / F657
页数:11
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