Celik Kavak Ebru, Gulcu Bulmus Funda, Bulmus Ozgur, Kavak Salih Burcin, Kocaman Nevin
Department of Obstetrics and Gynecology.
Vocational School of Health Services.
Drug Des Devel Ther. 2018 Feb 28;12:409-415. doi: 10.2147/DDDT.S157115. eCollection 2018.
The aim of the present study was to assess the protective effects of magnesium sulfate (MgSO) on ischemia/reperfusion (I/R) induced ovarian damage in a rat ovarian torsion model.
Forty-two female Sprague Dawley rats were included in the study. They were divided into six groups as Group 1, sham; Group 2, bilateral ovarian torsion; Group 3, bilateral ovarian torsion-detorsion; Group 4, MgSO-sham; Group 5, MgSO-bilateral ovarian torsion; Group 6, bilateral ovarian torsion-MgSO-detorsion. Both torsion and detorsion periods lasted 3 hours. In Groups 4, 5 and 6, MgSO (600 mg/kg) was administered by intraperitoneal route 30 minutes before sham operation, torsion and detorsion, respectively. At the end of the study period, both ovaries were removed. One of the ovaries was used for histopathological analyses and the other for biochemical analyses.
In the torsion-detorsion group, all the histopathological scores were higher compared to the sham and torsion only group (<0.05). Administration of MgSO only caused significant decrease in the inflammatory cell scores of the torsion-detorsion group (<0.05). MgSO, whether given before torsion or before detorsion, suppressed malondialdehyde levels when compared to the untreated groups (<0.01 and <0.001, respectively). Glutathione peroxidase activities were significantly higher in the MgSO applied torsion and detorsion groups than Groups 2 and 3 (<0.05, for both). Administration of MgSO also caused an increase in glutathione levels in the torsion and detorsion groups compared to the torsion only and detorsion only groups (<0.05, for both). Also, total oxidant status levels decreased in the MgSO applied torsion and detorsion groups compared to the untreated corresponding ones (<0.01 and <0.001, respectively). MgSO significantly decreased the Oxidative Stress Index levels in the torsion-detorsion group compared to Group 2 (<0.001).
Histopathological and biochemical analysis revealed that prophylactic treatment with MgSO reduces the changes observed in I/R injury in a rat model.
本研究旨在评估硫酸镁(MgSO)对大鼠卵巢扭转模型中缺血/再灌注(I/R)诱导的卵巢损伤的保护作用。
42只雌性斯普拉格-道利大鼠纳入本研究。它们被分为六组:第1组,假手术组;第2组,双侧卵巢扭转组;第3组,双侧卵巢扭转-复位组;第4组,MgSO-假手术组;第5组,MgSO-双侧卵巢扭转组;第6组,双侧卵巢扭转-MgSO-复位组。扭转和复位期均持续3小时。在第4、5和6组中,分别在假手术、扭转和复位前30分钟经腹腔途径给予MgSO(600mg/kg)。在研究期结束时,切除双侧卵巢。其中一个卵巢用于组织病理学分析,另一个用于生化分析。
在扭转-复位组中,与假手术组和仅扭转组相比,所有组织病理学评分均更高(<0.05)。仅给予MgSO可使扭转-复位组的炎症细胞评分显著降低(<0.05)。与未治疗组相比,无论在扭转前还是复位前给予MgSO,均可抑制丙二醛水平(分别为<0.01和<0.001)。MgSO应用于扭转和复位组的谷胱甘肽过氧化物酶活性显著高于第2组和第3组(两者均为<0.05)。与仅扭转组和仅复位组相比,给予MgSO还可使扭转和复位组的谷胱甘肽水平升高(两者均为<0.05)。此外,与未治疗的相应组相比,MgSO应用于扭转和复位组的总氧化剂状态水平降低(分别为<0.01和<0.001)。与第2组相比,MgSO可使扭转-复位组的氧化应激指数水平显著降低(<0.001)。
组织病理学和生化分析表明,MgSO预防性治疗可减轻大鼠模型中I/R损伤所观察到的变化。