依诺肝素对大鼠子宫缺血再灌注损伤的保护作用。

IF 1.3
Acta cirurgica brasileira Pub Date : 2025-09-29 eCollection Date: 2025-01-01 DOI:10.1590/acb407225
Duygu Lafci, Mustafa Hilmi Yaranoglu, Eren Altun, Eray Metin Guler, Ceyda Sancakli Usta
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摘要

目的:研究依诺肝素对实验性缺血再灌注损伤大鼠子宫的保护作用。方法:将30只雌性大鼠按体重和周期均质,分为对照组、缺血再灌注(I/R)组和缺血再灌注+依诺肝素(I/R+E)组。ⅰ/R组和ⅰ/R+E组分别建立实验性子宫I/R模型。与I/R组不同,I/R+E组大鼠在缺血前2小时皮下注射依诺肝素0.5 mg/kg。在组织病理学分析中,根据组织病理学评分系统对子宫内膜腺和内膜/子宫内膜间质改变进行评分。生物化学方面,测定子宫组织过氧化氢酶(CAT)、超氧化物歧化酶(SOD)活性和丙二醛(MDA)水平。结果:在组织病理学分析中,除坏死外,对照组的评分均低于其他组(p < 0.05)。I/R和I/R+E两组患者的腺体和间质变化无明显改善(p < 0.05)。但与I/R组相比,I/R+E组SOD和CAT活性显著升高,MDA水平显著降低(p = 0.000)。结论:依诺肝素虽对子宫I/R损伤无明显改善作用,但其抗氧化作用提示其对子宫I/R损伤的氧化应激具有保护作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Protective effects of enoxaparin treatment against uterus ischemia/reperfusion injury in rats.

Purpose: This study analyzed the protective effects of enoxaparin in rat uteruses by exposing the uterus to experimental ischemia-reperfusion injury.

Methods: Thirty female rats were homogenized by weight and cycle and divided into three groups: a control group, an ischemia-reperfusion (I/R) group, and an ischemia-reperfusion plus enoxaparin (I/R+E) group. An experimental uterine I/R model was established in the I/R and I/R+E groups. Unlike I/R group, all rats in the I/R+E group received subcutaneous enoxaparin at 0.5 mg/kg 2 hours before ischemia. In histopathological analysis, endometrial glandular and endo/myometrial stromal changes were scored according to the histopathological scoring system. Biochemically, catalase (CAT), superoxide dismutase (SOD) enzyme activities, and malondialdehyde (MDA) levels were measured in uterine tissues.

Results: In histopathological analysis, all of the control group's scores were lower than those of the other groups, except for necrosis (p 0.05). There was no significant improvement in the glandular and stromal changes between I/R and I/R+E (p 0.05). However, the I/R+E group showed significantly increased SOD and CAT activities and decreased MDA levels compared to the I/R group (p = 0.000).

Conclusion: Although enoxaparin did not significantly improve histopathological injury, its potent antioxidant effects suggest a protective role against oxidative stress in uterine I/R injury.

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