Protective Effect of Dexpanthenol on Ischemia-Reperfusion-Induced Renal Injury in Rats

被引:45
作者
Altintas, Ramazan [1 ]
Parlakpinar, Hakan [2 ]
Beytur, Ali [1 ]
Vardi, Nigar [3 ]
Polat, Alaadin [4 ]
Sagir, Mustafa [2 ]
Odabas, Gul Pelin [5 ]
机构
[1] Inonu Univ, Fac Med, Dept Urol, TR-44280 Malatya, Turkey
[2] Inonu Univ, Fac Med, Dept Pharmacol, TR-44280 Malatya, Turkey
[3] Inonu Univ, Fac Med, Dept Histol & Embryol, TR-44280 Malatya, Turkey
[4] Inonu Univ, Fac Med, Dept Physiol, TR-44280 Malatya, Turkey
[5] Inonu Univ, Fac Med, TR-44280 Malatya, Turkey
关键词
Dexpanthenol; Ischemia-reperfusion; Kidney; Oxidative stress; Rat; OXYGEN-FREE-RADICALS; ASCITES TUMOR-CELLS; PANTOTHENIC-ACID; ISCHEMIA/REPERFUSION INJURY; LIPID-PEROXIDATION; GLUTATHIONE; KIDNEY; PATHOPHYSIOLOGY; DYSFUNCTION; MECHANISMS;
D O I
10.1159/000343411
中图分类号
Q4 [生理学];
学科分类号
071003 [生理学];
摘要
Background/Aims: This experimental study was designed to investigate protective and therapeutic effects of Dexpanthenol (Dxp), an alcoholic analogue of pantothenic acid, on kidney damage induced by ischemia-reperfusion (I/R) in rats. Methods: Forty rats were randomly divided into a control group and 4 I/R groups (1 h ischemia followed by 23 h reperfusion). Three I/R groups were treated by Dxp (500 mg/kg, i.p.) at 3 different time points (before ischemia, during ischemia and late reperfusion). The histopathological findings including apoptotic changes, and also tissue malondialdehyde (MDA), superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPX), blood urea nitrogen (BUN), serum creatinine (Cr) and albumin (Alb) levels were determined. Results: Kidney tissue MDA levels were found to be significantly higher in the I/R group, whereas the values of GPX were lower when compared to the control group. The levels of SOD and CAT did not reach to statistical meaning level in I/R group. Dxp given during ischemia reduced the elevated MDA levels to the nearly control levels and this ameliorating effect was found as parallel to the result of GPX. Serum levels of BUN and Cr were significantly higher in I/R group. Dxp given during ischemia significantly reduced the elevated BUN and Cr levels when compared to I/R group. Renal I/R injury also induced extensive tubular necrosis, glomerular damage and apoptosis in the histological evaluation. Dxp ameliorated these histological damages in different amounts in all treatment groups. Conclusion: In this study the protective effects of Dxp against renal I/R injury has been evaluated for the first time. Copyright (c) 2012 S. Karger AG, Basel
引用
收藏
页码:220 / 230
页数:11
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