Pretreatment of sildenafil attenuates ischemia-reperfusion renal injury in rats

被引:99
作者
Choi, Dae Eun [1 ]
Jeong, Jin Young [1 ]
Lim, Beom Jin [2 ]
Chung, Sarah [1 ]
Chang, Yoon Kyung [3 ]
Lee, Sang Ju [3 ]
Na, Ki Ryang [1 ]
Kim, Seok Young [3 ]
Shin, Young Tai [1 ]
Lee, Kang Wook [1 ]
机构
[1] Chungnam Natl Univ Hosp, Taejon, South Korea
[2] Gangnam Severance Hosp, Seoul, South Korea
[3] Daejeon St Mary Hosp, Taejon, South Korea
关键词
apoptosis; ERK; NITRIC-OXIDE SYNTHASE; PHOSPHODIESTERASE-5; INHIBITION; ISCHEMIA/REPERFUSION INJURY; HYPOXIA/REOXYGENATION INJURY; HEART-FAILURE; KIDNEY; APOPTOSIS; CARDIOPROTECTION; TRANSPLANTATION; ACTIVATION;
D O I
10.1152/ajprenal.90609.2008
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Choi DE, Jeong JY, Lim BJ, Chung S, Chang YK, Lee SJ, Na KR, Kim SY, Shin YT, Lee KW. Pretreatment of sildenafil attenuates ischemia-reperfusion renal injury in rats. Am J Physiol Renal Physiol 297: F362-F370, 2009. First published May 27, 2009; doi:10.1152/ajprenal.90609.2008.-Sildenafil was the first selective inhibitor of phosphodiesterase-5 (PDE5) to be widely used for treating erectile dysfunction. Many recent studies have investigated the cardioprotective role of sildenafil in animal models. We evaluated the protective effects of sildenafil in experimental renal ischemia-reperfusion (IR) injury in two studies. In study 1, male Sprague-Dawley rats were divided into four groups: sham, sildenafil-treated sham, vehicle-treated IR, and sildenafil-treated IR groups. In study 2, we divided the rats into two groups: sildenafil-treated IR rats and PD98059 (ERK inhibitor) + sildenafil-treated IR rats. Functional parameters of the kidney were evaluated at the molecular and structural levels. Blood urea nitrogen (BUN) and serum creatinine levels were lower in sildenafil-treated IR rats than in vehicle-treated IR rats. The expression of inducible (iNOS) and endothelial nitric oxide synthase (eNOS) proteins in sildenafil-treated IR rats was significantly higher than in vehicle-treated IR rats. Pretreatment with sildenafil in IR rats increased ERK phosphorylation and reduced the renal Bax/Bcl-2 ratio, renal caspase-3 activity, and terminal dUTP nick end-labeling-positive apoptotic cells. In contrast, PD98059 treatment increased BUN and serum creatinine levels and attenuated the sildenafil-induced expression of pERK, iNOS, eNOS, and Bcl-2. PD98059 also increased caspase-3 activity but did not decrease the sildenafil-induced accumulation of cGMP. In conclusion, this study suggests that sildenafil has antiapoptotic effects in experimental IR renal injury via ERK phosphorylation, induction of iNOS and eNOS production, and a decrease in the Bax/Bcl-2 ratio.
引用
收藏
页码:F362 / F370
页数:9
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