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Protective effect of lisinopril on hepatic ischemia/reperfusion injury in rats.

机译:赖诺普利对大鼠肝缺血/再灌注损伤的保护作用。

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OBJECTIVE: Ischemia/reperfusion (I/R) injury plays a key role in the pathogenesis of hepatic failure in several clinical settings such as liver resection or transplantation. Lisinopril, a widely prescribed drug for various cardiovascular conditions, has been reported to have diverse pharmacological properties. The aim of this study, therefore, was to evaluate a potential protective effect of lisinopril on hepatic I/R injury in rats. MATERIALS AND METHODS: In anesthetized rats, partial hepatic ischemia was applied for one hour followed by two hours reperfusion. Biochemical analysis of serum and hepatic tissue was done. Hepatic tissue was also subjected to electron microscopy. RESULTS: Pre-ischemic treatment with lisinopril (10 mg/kg) exerted protection against I/R-induced hepatocellular injury as evident by significant decrease in serum alanine aminotransferase (ALT), aspartate aminotransferase (AST), and total bilirubin levels, along with hepatic lipid peroxidation, expressed as malondialdehyde content, with a concurrent increase in hepatic nitric oxide content as compared to I/R group. The electron microscopic examination indicated that lisinopril can effectively protect against hepatic I/R injury. CONCLUSION: Lisinopril provides a protection against hepatic I/R injury in rats. The protective effect is associated with reduction of oxidative stress-induced lipid peroxidation level and enhancement of nitric oxide availability.
机译:目的:缺血/再灌注(I / R)损伤在肝切除或移植等几种临床环境中在肝衰竭的发病机理中起着关键作用。据报道,利诺普利是一种用于各种心血管疾病的广泛处方药,具有多种药理特性。因此,本研究的目的是评估赖诺普利对大鼠肝I / R损伤的潜在保护作用。材料与方法:在麻醉的大鼠中,局部肝缺血1小时,然后再灌注2小时。对血清和肝组织进行了生化分析。肝组织也接受电子显微镜检查。结果:赖诺普利(10 mg / kg)缺血前治疗对I / R诱导的肝细胞损伤具有保护作用,血清丙氨酸氨基转移酶(ALT),天冬氨酸氨基转移酶(AST)和总胆红素水平显着降低,以及肝脂质过氧化,以丙二醛含量表示,与I / R组相比,肝一氧化氮含量同时增加。电子显微镜检查表明赖诺普利可有效预防肝I / R损伤。结论:利诺普利可预防大鼠肝I / R损伤。该保护作用与氧化应激诱导的脂质过氧化水平的降低和一氧化氮利用率的提高有关。

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