1. The protective effects of tadalafil on renal damage following ischemia reperfusion injury in rats.
- Author
-
Erol B, Turker T, Tok A, Bektas S, Mungan G, Ozkanli S, Karakas B, Tokgoz H, Akduman B, and Mungan A
- Subjects
- Animals, Antioxidants metabolism, Apoptotic Protease-Activating Factor 1 metabolism, Immunohistochemistry, Kidney drug effects, Kidney Tubules drug effects, Kidney Tubules enzymology, Kidney Tubules pathology, Malondialdehyde blood, Nitric Oxide Synthase Type II metabolism, Nitric Oxide Synthase Type III metabolism, Protective Agents pharmacology, Rats, Wistar, Reperfusion Injury blood, Reperfusion Injury pathology, Tadalafil, Kidney pathology, Protective Agents therapeutic use, Reperfusion Injury drug therapy
- Abstract
Ischemia-reperfusion injury can cause renal damage, and phosphodiesterase inhibitors are reported to regulate antioxidant activity. We investigated the prevention of renal damage using tadalafil after renal ischemia reperfusion (I/R) injury in rats. A total of 21 adult male Wistar albino rats were randomly divided into three groups of seven, including Group 1-control, Group 2-I/R, and Group 3-tadalafil + I/R group (I/R-T group) received tadalafil intraperitoneally at 30 minutes before ischemia. Inducible nitric oxide synthase, endothelial nitric oxide synthase, malondialdehyde, and total antioxidant capacity levels were evaluated, and histopathological changes and apoptosis in the groups were examined. Tadalafil decreased malondialdehyde levels in the I/R group and increased the total antioxidant capacity level. Histopathological and immunohistochemical findings revealed that tadalafil decreased renal injury scores and the ratios of injured cells, as measured through apoptotic protease activating factor 1, inducible nitric oxide synthase, and endothelial nitric oxide synthase levels. We suggest that tadalafil has protective effects against I/R-related renal tissue injury., (Copyright © 2015. Published by Elsevier Taiwan.)
- Published
- 2015
- Full Text
- View/download PDF