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地奥司明改善大鼠肝缺血再灌注诱导的肠道损伤。

Diosmin ameliorates intestinal injury induced by hepatic ischemia reperfusion in rats.

作者信息

Tanrikulu Y, Kismet K, Serin Kilicoglu S, Devrim E, Erel S, Sen Tanrikulu C, Dinc S, Edebal O H, Erdemli E, Akkus M A

机构信息

Ankara Training and Research Hospital Department of 4th General Surgery, Ankara, Turkey.

出版信息

Bratisl Lek Listy. 2011;112(10):545-51.

Abstract

BACKGROUND

Hepatic ischemia-reperfusion causes histologic injury to the intestinal mucosa. We investigated the effects of diosmin, a phelobotrophic drug with antioxidant and antiinflammatory effects, on intestinal injury in the experimental liver ischemia-reperfusion model.

MATERIALS AND METHODS

Fourty rats were divided into four groups: sham group (Group 1), control group (Group 2), perop diosmin group (50 mg/kg) treatment group (Group 3) and preop 10-day diosmin (50 mg/kg) treatment group (Group 4). Ischemia-reperfusion model was carried out by clamping the hepatic pedicle for 60 min and then reperfusing the liver for 90 min. At the end of procedures, blood and ileum tissue samples were obtained for biochemical and histopathological assessments.

RESULTS

According to the results of liver function tests (AST, ALT and LDH) there was a significant difference between the control and other groups (p < 0.001 for all). According to the plasma and ileum oxidative stress parameters (MDA, GSH-Px and XO), there was a significant difference between the control and other groups (p < 0.05 for all). Histopathologically; the specimens in Group 2 showed specific morphological abnormalities (the epithelial lining of the apical surface of villi was degenerated and desquamated to the lumen). Group 3 and 4 showed ileal histomorphology similar to the sham group. Pathological scores were significantly different between Group 2 and other groups.

CONCLUSIONS

Diosmin can be administered for protection from destructive effects of hepatic ischemia-reperfusion injury on intestine in both emergent and elective hepatic surgical operations in which the possible ischemic periods are expected (Tab. 4, Fig. 1, Ref. 39).

摘要

背景

肝脏缺血再灌注会导致肠黏膜组织学损伤。我们研究了地奥司明(一种具有抗氧化和抗炎作用的血管保护药物)对实验性肝脏缺血再灌注模型中肠损伤的影响。

材料与方法

40只大鼠分为四组:假手术组(第1组)、对照组(第2组)、术中给予地奥司明组(50mg/kg)治疗组(第3组)和术前10天给予地奥司明(50mg/kg)治疗组(第4组)。通过夹闭肝蒂60分钟,然后再灌注肝脏90分钟建立缺血再灌注模型。在操作结束时,获取血液和回肠组织样本进行生化和组织病理学评估。

结果

根据肝功能测试结果(AST、ALT和LDH),对照组与其他组之间存在显著差异(所有p<0.001)。根据血浆和回肠氧化应激参数(MDA、GSH-Px和XO),对照组与其他组之间存在显著差异(所有p<0.05)。组织病理学上,第2组标本显示出特定的形态学异常(绒毛顶端表面的上皮衬里退化并脱落到管腔中)。第3组和第4组显示回肠组织形态与假手术组相似。第2组与其他组之间的病理评分有显著差异。

结论

在预期可能出现缺血期的急诊和择期肝脏手术中,地奥司明可用于保护肠道免受肝脏缺血再灌注损伤的破坏作用(表4,图1,参考文献39)。

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