Olmesartan Attenuates Tacrolimus-Induced Biochemical and Ultrastructural Changes in Rat Kidney Tissue

被引:12
作者
Al-Harbi, Naif O. [1 ]
Imam, Faisal [1 ]
Al-Harbi, MohammedM. [1 ]
Iqbal, Muzaffar [2 ]
Nadeem, Ahmed [1 ]
Sayed-Ahmed, MohammedM. [1 ]
Alabidy, Ali D. [3 ]
Almukhallafi, Ali F. [4 ]
机构
[1] King Saud Univ, Coll Pharm, Dept Pharmacol & Toxicol, Riyadh 11451, Saudi Arabia
[2] King Saud Univ, Coll Pharm, Dept Pharmaceut Chem, Riyadh 11451, Saudi Arabia
[3] El Ghad Int Coll Hlth Sci, Riyadh 11451, Saudi Arabia
[4] Al Haya Med Co, Riyadh 11411, Saudi Arabia
关键词
DOXORUBICIN-INDUCED NEPHROTOXICITY; ADRIAMYCIN-INDUCED CARDIOTOXICITY; FK506; NEPHROTOXICITY; HEART-FAILURE; RENAL-DISEASE; ANGIOTENSIN; CYCLOSPORINE; INHIBITION; EXPRESSION; ALISKIREN;
D O I
10.1155/2014/607246
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Tacrolimus, a calcineurin inhibitor, is clinically used as an immunosuppressive agent in organ transplantation, but its use is limited due to its marked nephrotoxicity. The present study investigated the effect of olmesartan (angiotensin receptor blocker) on tacrolimus-induced nephrotoxicity in rats. A total of 24 rats were divided into four groups, which included control, tacrolimus, tacrolimus + olmesartan, and olmesartan groups. Tacrolimus-induced nephrotoxicity was assessed biochemically and histopathologically. Tacrolimus significantly increased BUN and creatinine level. Treatment with olmesartan reversed tacrolimus-induced changes in the biochemical markers (BUN and creatinine) of nephrotoxicity. Tacrolimus significantly decreased GSH level and catalase activity while increasing MDA level. Olmesartan also attenuated the effects of tacrolimus on MDA, GSH, and catalase. In tacrolimus group histological examination showed marked changes in renal tubule, mitochondria, and podocyte processes. Histopathological and ultrastructural studies showed that treatment with olmesartan prevented tacrolimus-induced renal damage. These results suggest that olmesartan has protective effects on tacrolimus-induced nephrotoxicity, implying that RAS might be playing role in tacrolimus-induced nephrotoxicity.
引用
收藏
页数:7
相关论文
共 46 条
[1]   THERAPEUTIC ADVANTAGE OF CONVERTING ENZYME-INHIBITORS IN ARRESTING PROGRESSIVE RENAL-DISEASE ASSOCIATED WITH SYSTEMIC HYPERTENSION IN THE RAT [J].
ANDERSON, S ;
RENNKE, HG ;
BRENNER, BM .
JOURNAL OF CLINICAL INVESTIGATION, 1986, 77 (06) :1993-2000
[2]   RENAL RENIN-ANGIOTENSIN SYSTEM IN DIABETES - FUNCTIONAL, IMMUNOHISTOCHEMICAL, AND MOLECULAR BIOLOGICAL CORRELATIONS [J].
ANDERSON, S ;
JUNG, FF ;
INGELFINGER, JR .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 265 (04) :F477-F486
[3]  
Bae E.H., 2013, J RENIN ANGIOTENSIN
[4]  
Claiborne A., 1985, CRC handbook of methods for oxygen radical research, V1, P283, DOI DOI 10.1016/0531-5565(85)90021-X
[5]   Tacrolimus reduces nitric oxide synthase function by binding to FKBP rather than by its calcineurin effect [J].
Cook, Leslie G. ;
Chiasson, Valorie L. ;
Long, Cheng ;
Wu, Gang-Yi ;
Mitchell, Brett M. .
KIDNEY INTERNATIONAL, 2009, 75 (07) :719-726
[6]   Silymarin prevents adriamycin-induced cardiotoxicity and nephrotoxicity in rats [J].
El-Shitany, Nagla A. ;
El-Haggar, Sahar ;
El-Desoky, Karema .
FOOD AND CHEMICAL TOXICOLOGY, 2008, 46 (07) :2422-2428
[7]   Long-term ACE-inhibitor therapy in patients with heart failure or left-ventricular dysfunction:: a systematic overview of data from individual patients [J].
Flather, MD ;
Yusuf, S ;
Kober, L ;
Pfeffer, M ;
Hall, A ;
Murray, G ;
Torp-Pedersen, C ;
Ball, S ;
Pogue, J ;
Moyé, L ;
Braunwald, E .
LANCET, 2000, 355 (9215) :1575-1581
[8]   Protective effect of telmisartan against cadmium-induced nephrotoxicity in mice [J].
Fouad, Amr A. ;
Jresat, Iyad .
LIFE SCIENCES, 2011, 89 (1-2) :29-35
[9]   Aliskiren, a novel orally effective renin inhibitor, provides dose-dependent antihypertensive efficacy and placebo-like tolerability in hypertensive patients [J].
Gradman, AH ;
Schmieder, RE ;
Lins, RL ;
Nussberger, J ;
Chiang, YT ;
Bedigian, MP .
CIRCULATION, 2005, 111 (08) :1012-1018
[10]   The Role of Angiotensin II Receptor 1 (AT1) Blockade in Cisplatin-Induced Nephrotoxicity in Rats: Gender-Related Differences [J].
Haghighi, Maryam ;
Nematbakhsh, Mehdi ;
Talebi, Ardeshir ;
Nasri, Hamid ;
Ashrafi, Farzaneh ;
Roshanaei, Kambiz ;
Eshraghi-Jazi, Fatemeh ;
Pezeshki, Zahra ;
Safari, Tahereh .
RENAL FAILURE, 2012, 34 (08) :1046-1051