依托咪酯减轻大鼠卵巢缺血再灌注损伤

Vildan Kölükçü, Mehtap Gürler Balta, Hakan Tapar, Tuğba Karaman, Serkan Karaman, Velid Unsal, Fikret Gevrek, Muzaffer Katar
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摘要

背景:本研究探讨依托咪酯在卵巢缺血再灌注损伤实验模型中对氧化损伤的保护作用:本研究探讨依托咪酯在卵巢缺血再灌注损伤实验模型中对氧化损伤的保护作用:方法:将 24 只雌性大鼠随机分为三组。第一组为对照组。第 2 组接受卵巢扭转/剥离术。第 3 组接受与第 2 组类似的手术;此外,在卵巢剥离前 30 分钟腹腔注射 4 毫克/千克依托咪酯。对血液样本进行脂质过氧化、促炎细胞因子水平和抗氧化酶活性分析 结果:血液样本的生化分析表明,与第二组相比,第三组的促炎细胞因子,包括白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)和肿瘤坏死因子-α(TNF-α)均有所下降(p=0.005、p=0.016 和 pConclusion):依托咪酯能减轻大鼠卵巢扭转-扭转模型的缺血再灌注损伤,改善组织病理学和生化结果。
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Etomidate alleviates ovarian ischemia-reperfusion injury in rats.

Background: This study investigates the protective effects of etomidate against oxidative damage in an experimental model of ovarian ischemia-reperfusion injury.

Methods: A total of 24 female rats were randomized into three groups. Group 1 served as the control. Group 2 underwent an ovarian torsion/detorsion procedure. Group 3 underwent similar procedures as Group 2; additionally, 4 mg/kg of etomidate was administered intraperitoneally 30 minutes before ovarian detorsion. Blood samples were analyzed for lipid peroxidation, pro-inflammatory cytokine levels, and antioxidant enzyme activity RESULTS: Biochemical analysis of blood samples revealed reductions in pro-inflammatory cytokines, including interleukin-1 Beta (IL-1β), interleukin-6 (IL-6), and tumor necrosis factor-alpha (TNF-α), in Group 3 compared to Group 2 (p=0.005, p=0.016, and p<0.001, respectively). Additionally, a decrease in malondialdehyde (MDA) levels was observed in Group 3 compared to Group 2 (p<0.001). In contrast, activities of antioxidant enzymes, including superoxide dismutase (SOD) and glutathione peroxidase (GSH-PX), were significantly increased in Group 3 compared to Group 2 (p=0.031 and p=0.001, respectively). Furthermore, Group 3 demonstrated notable reductions in histopathological scores for follicular degeneration, vascular occlusion, bleeding, and inflammation compared to Group 2 (p<0.001, p<0.001, p<0.001, and p=0.001, respectively).

Conclusion: Etomidate alleviates ischemia-reperfusion injury in a rat ovarian torsion-detorsion model by improving both histopathological and biochemical outcomes.

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