流产患者胎盘组织中自由基清除酶活性和脂质过氧化的研究。

Aydan Biri, Mustafa Kavutcu, Nuray Bozkurt, Erdinç Devrim, Nilhan Nurlu, Iker Durak
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引用次数: 35

摘要

背景:流产(早孕失败)是一种与妊娠相关的疾病,其病理生理机制尚未完全了解。脂质过氧化和抗氧化酶活性的改变可能在这种疾病的发病机制中起重要作用。本研究旨在探讨流产胎盘组织中自由基清除酶活性与脂质过氧化水平之间的可能关系。方法:取21例流产患者和25例正常妊娠择期流产患者的胎盘组织标本作为对照组。测定胎盘组织中总超氧化物歧化酶(T-SOD)、谷胱甘肽过氧化物酶(GSH-Px)、过氧化氢酶(CAT)活性、硫代巴比妥酸活性物质(TBARS)水平、抗氧化电位(AOP)和非酶超氧化物自由基清除剂活性(NSSA)。结果:与选择性流产组相比,早孕失败组GSH-Px、CAT活性、TBARS水平明显升高,T-SOD、NSSA水平明显降低。然而,两组之间在AOP水平上没有显著差异。结论:我们的研究结果反映了妊娠早期失败胎盘组织中的氧化应激,因为氧化过程似乎被抗氧化酶如CAT和GSH-Px的生理激活所抵消。此外,一种代偿机制可能针对流产患者可能出现的氧化损伤。
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Investigation of free radical scavenging enzyme activities and lipid peroxidation in human placental tissues with miscarriage.

Background: Miscarriage (early pregnancy failure) is a pregnancy-related disease, the pathophysiology of which is still not completely understood. Lipid peroxidation and alterations in antioxidant enzyme activities may be of importance in the pathogenesis of this disorder. This study was planned to investigate the possible relation between free radical scavenging enzyme activities and lipid peroxidation levels in placenta tissues with miscarriage.

Methods: Placental tissue samples were obtained from 21 patients who had miscarried and 25 normal pregnant women undergoing elective abortion as a control group. Total superoxide dismutase (T-SOD), glutathione peroxidase (GSH-Px), and catalase (CAT) enzyme activities and levels of thiobarbituric acid reactive substances (TBARS), antioxidant potential (AOP), and nonenzymatic superoxide radical scavenger activity (NSSA) were measured in the placental tissues.

Results: GSH-Px, CAT activities, and TBARS levels were found to be significantly increased, while T-SOD and NSSA values decreased in patients with early pregnancy failure when compared with women undergoing elective abortion (control group). However, there were no significant differences in AOP levels between the groups.

Conclusions: Our results reflect oxidative stress in placenta tissues of early pregnancy failure, as the oxidative processes seem to be counteracted by the physiologic activation of antioxidant enzymes such as CAT and GSH-Px. Moreover, a compensatory mechanism might be developed against possible oxidative damage in patients with miscarriage.

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