Department of Pharmacology, Smt. R. B. Patel Mahila Pharmacy College, S.N.D.T. Women's University, Atkot, Rajkot, Gujarat, India.
Ren Fail. 2010;32(9):1088-94. doi: 10.3109/0886022X.2010.504911.
It was demonstrated that fenofibrate and telmisartan exerted renoprotective effects in ischemia/reperfusion (I/R) injury. Because the combination of fenofibrate and telmisartan synergistically enhanced peroxisome proliferator-activated receptor (PPAR) activation, we hypothesized that the combination of both drugs may exert prolonged beneficial effects in renal I/R injury than fenofibrate alone. Forty-eight male Wistar albino rats were divided into eight groups. Hyperlipidemia was induced by cholesterol feeding for 4 weeks. At the end of the fourth week, renal I/R injury was performed by occlusion of both renal vascular pedicles for 60 minutes, followed by 24 hours of reperfusion. In the treatment group, fenofibrate alone and in combination with telmisartan was administered 2 weeks prior to renal ischemia. At the end of the experiment, blood and kidneys were isolated for biochemical and histological analysis. I/R in hyperlipidemic rat shows significantly increased lipid peroxidation, nitric oxide, and myeloperoxidase activity, and depletion of antioxidant enzyme compared with control rats, and that was significantly restored after fenofibrate and telmisartan treatment. Also, significant increases in serum homocysteine level were detected following I/R. Fenofibrate treatment further elevated homocysteine level, which was reduced by telmisartan in combination with fenofibrate. The most significant histological damage was found in the hyperlipidemic rat subjected to renal I/R, which was reduced significantly with combination therapy. The results of this study concluded that fenofibrate alone and in combination with telmisartan significantly ameliorated renal I/R injury. The additive beneficial effect of telmisartan is predicted to reduce homocysteine-induced oxidative stress through reduced nitric oxide production during I/R.
已经证实,非诺贝特和替米沙坦在缺血/再灌注(I/R)损伤中具有肾保护作用。由于非诺贝特和替米沙坦联合使用可协同增强过氧化物酶体增殖物激活受体(PPAR)的激活,我们假设这两种药物的联合使用可能比单独使用非诺贝特在肾 I/R 损伤中产生更持久的有益效果。48 只雄性 Wistar 白化大鼠被分为 8 组。通过给予胆固醇饮食 4 周来诱导高血脂症。在第 4 周结束时,通过夹闭双侧肾血管蒂 60 分钟来进行肾 I/R 损伤,然后再进行 24 小时的再灌注。在治疗组中,在肾缺血前 2 周单独给予非诺贝特和与替米沙坦联合使用。在实验结束时,分离血液和肾脏进行生化和组织学分析。与对照组大鼠相比,高脂血症大鼠的 I/R 显示脂质过氧化、一氧化氮和髓过氧化物酶活性显著增加,抗氧化酶耗竭,而非诺贝特和替米沙坦治疗后则显著恢复。此外,还检测到 I/R 后血清同型半胱氨酸水平显著升高。非诺贝特治疗进一步升高了同型半胱氨酸水平,而替米沙坦与非诺贝特联合使用则降低了该水平。在接受肾 I/R 的高脂血症大鼠中发现最显著的组织学损伤,联合治疗可显著减轻该损伤。这项研究的结果表明,非诺贝特单独和联合替米沙坦可显著改善肾 I/R 损伤。替米沙坦的附加有益作用预计通过减少 I/R 期间的一氧化氮产生来减少同型半胱氨酸诱导的氧化应激。