Schipper H M, Desjardins G C, Beaudet A, Brawer J R
Department of Anatomy and Cell Biology, Bloomfield Centre for Research in Aging, Jewish General Hospital, McGill University, Montreal, Que., Canada.
Brain Res. 1994 Jul 25;652(1):161-3. doi: 10.1016/0006-8993(94)90332-8.
A single intramuscular injection of 2 mg estradiol valerate (EV) results in neuronal degeneration and beta-endorphin depletion in the hypothalamic arcuate nucleus of adult female rats. We have hypothesized that peroxidase-positive astrocytes in this brain region oxidize estrogens and catecholestrogens to semiquinone radicals which mediate oxidative neuronal injury. In the present study, dietary administration of the potent antioxidant 21-aminosteroid, U-74389F, completely blocked EV-induced beta-endorphin depletion in the hypothalami of adult female rats. Neither EV nor 21-aminosteroid treatment had any effect on hypothalamic concentrations of neuropeptide Y and Met-enkephalin, confirming that the estradiol lesion is fairly selective for the beta-endorphin cell population. The present findings support the hypothesis that the toxic effect of estradiol on hypothalamic beta-endorphin neurons is mediated by free radicals.
单次肌肉注射2毫克戊酸雌二醇(EV)会导致成年雌性大鼠下丘脑弓状核中的神经元变性和β-内啡肽耗竭。我们推测,该脑区中过氧化物酶阳性星形胶质细胞会将雌激素和儿茶酚雌激素氧化为半醌自由基,从而介导氧化性神经元损伤。在本研究中,通过饮食给予强效抗氧化剂21-氨基类固醇U-74389F,完全阻断了成年雌性大鼠下丘脑内EV诱导的β-内啡肽耗竭。EV和21-氨基类固醇处理均对下丘脑神经肽Y和甲硫氨酸脑啡肽的浓度没有任何影响,证实雌二醇损伤对β-内啡肽细胞群体具有相当的选择性。本研究结果支持以下假设:雌二醇对下丘脑β-内啡肽神经元的毒性作用是由自由基介导的。