Zonguldak Karaelmas University, Medical School, Department of Physiology, Kozlu, Zonguldak, Turkey.
Physiol Res. 2009;58(6):909-912. doi: 10.33549/physiolres.931647. Epub 2008 Dec 17.
Neuroprotective effects of estrogens and progesterone have been widely studied in various experimental models. The present study was designed to compare possible neuroprotective effects of 17alpha-estradiol, 17beta-estradiol, and progesterone on oxidative stress in rats subjected to global cerebral ischemia. Global cerebral ischemia was induced in ovariectomized female rats by four vessel occlusion for 10 min. Following 72 h of reperfusion, levels of malondialdehyde (MDA, oxidative stress marker), and reduced glutathione (GSH, major endogenous antioxidant) were assessed in hippocampus, striatum and cortex of rats treated with either 17alpha-estradiol, 17beta-estradiol, progesterone or estradiol + progesterone beforehand. Steroid administration ameliorated ischemia-induced decrease in GSH and increase in MDA levels. Our data offers additional evidence that estrogens and progesterone or combination of two exert a remarkable neuroprotective effect reducing oxidative stress.
雌激素和孕激素的神经保护作用在各种实验模型中得到了广泛研究。本研究旨在比较 17α-雌二醇、17β-雌二醇和孕酮对 4 血管闭塞 10 分钟诱导的雌性去卵巢大鼠全脑缺血后氧化应激的可能神经保护作用。72 小时再灌注后,检测预先给予 17α-雌二醇、17β-雌二醇、孕酮或雌二醇+孕酮的大鼠海马、纹状体和皮质中丙二醛(MDA,氧化应激标志物)和还原型谷胱甘肽(GSH,主要内源性抗氧化剂)的水平。类固醇给药改善了缺血诱导的 GSH 降低和 MDA 水平升高。我们的数据提供了额外的证据,表明雌激素和孕激素或两者的组合具有显著的神经保护作用,可降低氧化应激。