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https://hdl.handle.net/11499/6429
Title: | Antiapoptotic effect of angiotensin-II type-1 receptor blockade in renal tubular cells of hyperoxaluric rats | Authors: | Tunçdemir, M. Demirkesen, O. Öztürk, M. Atukeren, P. Koray Gümüstas, M. Turan, Tahir |
Keywords: | Apoptosis AT1 receptor blocker Hyperoxaluria Kidney Rat angiotensin 1 receptor caspase 3 ethylene glycol losartan protein Bax protein bcl 2 transforming growth factor beta1 animal experiment animal model animal tissue apoptosis article blood analysis controlled study drug mechanism histopathology hyperoxaluria immunohistochemistry immunoreactivity kidney tubule cell kidney tubule damage male nonhuman priority journal rat urine level Angiotensin II Type 1 Receptor Blockers Animals Kidney Tubules Losartan Male Rats Rats, Wistar |
Abstract: | In this study, we investigated the protective effect of losartan as an AT1 receptor antagonist by evaluating the expression of apoptosis-regulatory genes that contribute to the progressive damage in the renal tubules of hyperoxaluric rats. Rats were divided into 4 groups of 10 each; control (C), ethylene glycol (EG), ethylene glycol + losartan (EG + L) and Losartan (L). For 4 weeks 0.8% EG, as a precursor for oxalate, was administered to EG and EG + L and losartan (300 mg/l) was administered to groups EG + L and L. Urine and blood samples were collected for biochemical determination. Bcl-2, bax, caspase-3 and TGF-beta 1 antibodies were used for immunohisto-chemistry. Apoptosis was determined by TUNEL method. A marked increase in urinary oxalate levels of the rats in EG and EG + L groups was found. In the EG group a diffuse amount of oxalate crystals into the tubular lumina and interstitium in the cortex was observed. In the EG group GBM thickening, interstitial fibrosis and tubular atrophy with infiltration of mononuclear cell findings reduced in the EG + L group were presented as well. In the EG group, immunoreactivity of TGF-beta 1 was increased in glomeruli and tubuli. In the EG + L group, immunoreactivity of TGF-beta 1 was decreased compared to the EG group. Bax expression increased in the renal tubules of EG group and reduced in the EG + L group comparing to the control. In the EG + L group, the immunoreactivity of bcl-2 was increased in glomeruli. In EG + L treated group, number of caspase-3 immunopositive cells were decreased compared to all groups (P < 0.01). Apoptotic cells were increased in the EG-treated group compared to the other groups. Decreased apoptotic cell number was observed in the EG + L compared to the EG group (P < 0.01). Our findings suggest that losartan may provide a beneficial effect against tubulointerstitial damage and decrease renal tubular apoptosis caused by hyperoxaluria. © Springer-Verlag 2010. | URI: | https://hdl.handle.net/11499/6429 https://doi.org/10.1007/s00240-010-0255-8 |
ISSN: | 0300-5623 |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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