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Study of the protective effect of ischemic and pharmacological preconditioning on hepatic ischemic reperfusion injury induced in rats

机译:缺血和药物预处理对大鼠肝缺血再灌注损伤的保护作用研究

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Background and Aim Hepatic ischemia reperfusion injury is the main cause of liver failure following liver surgery, so an effective method is needed to prevent or reduce this hepatic injury. The aim of the present study is to investigate the potential effect of ischemic preconditioning versus pharmacological preconditioning with lisinopril or verapamil for protection against hepatic ischemia reperfusion injury induced in rats. Methods Rats were divided into six groups. Group I served as control untreated. Rats of group II were subjected to laparotomy without induction of ischemia reperfusion. Ischemia reperfusion by ligation of the portal trait for 30?min, followed by reperfusion for 2?h, was performed in rats of groups III–VI. Ischemic preconditioning was performed for rats of group IV before induction of ischemia reperfusion. Lisinopril and verapamil was given daily for 3?days before induction of ischemia reperfusion in groups V and VI, respectively. Serum level of liver transaminases and liver malondialdehyde content were measured, and hepatic histopathological examination was assessed. Results Induction of ischemia reperfusion resulted in significant elevation of liver transaminases and liver malondialdehyde content associated with significant hepatic histopathological injury that were significantly improved by ischemic preconditioning, lisinopril, or verapamil treatment. Verapamil showed the most significant improvement compared with ischemic preconditioning or lisinopril treatment. Conclusion Ischemic preconditioning and pharmacological preconditioning by lisinopril or verapamil can protect against hepatic ischemia reperfusion probably through inhibition of oxidative stress and neutrophil infiltration. The most potent protection is demonstrated by verapamil treatment.
机译:背景与目的肝缺血再灌注损伤是肝手术后肝衰竭的主要原因,因此需要一种有效的方法来预防或减轻这种肝损伤。本研究的目的是研究缺血预处理与赖氨普利或维拉帕米药理预处理对大鼠肝缺血再灌注损伤的潜在保护作用。方法将大鼠分为六组。第一组作为未经处理的对照。对第II组的大鼠进行剖腹手术而不诱导缺血再灌注。在III-VI组大鼠中,通过结扎门静脉性状30分钟,再灌注2小时,进行缺血再灌注。在诱导缺血再灌注之前,对IV组的大鼠进行缺血预处理。 V组和VI组分别在诱导局部缺血再灌注前3天,每天给予Lisinopril和维拉帕米。测量血清肝转氨酶水平和肝丙二醛含量,并评估肝组织病理学检查。结果诱导缺血再灌注导致肝脏转氨酶和肝脏丙二醛含量显着升高,并伴有严重的肝脏组织病理学损伤,缺血预处理,赖诺普利或维拉帕米治疗可显着改善。与缺血预处理或赖诺普利治疗相比,维拉帕米显示出最显着的改善。结论赖诺普利或维拉帕米进行的缺血预处理和药理预处理可能通过抑制氧化应激和中性粒细胞浸润来预防肝缺血再灌注。维拉帕米治疗显示出最有效的保护作用。

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