Dehydroepiandrosterone protects hippocampal neurons against neurotoxin-induced cell death: Mechanism of action
Dehydroepiandrosterone protects hippocampal neurons against neurotoxin-induced cell death: Mechanism of action
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DOI：
10.1046/j.1525-1373.1999.d01-124.x
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发表时间：
1999-11-01
影响因子：
--
通讯作者：
Kalimi, M
中科院分区：
文献类型：
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作者：
Cardounel, A;Regelson, W;Kalimi, M
Dehydroepiandrosterone (DHEA), an adrenal cortex hormone secreted in large quantities in humans, protects cells of the clonal mouse hippocampal cell line HT-22 against the excitatory amino acid glutamate (5 mM), and amyloid beta-protein (2 mu M) toxicity in a dose-dependent manner with optimum protection obtained at 5 mu M concentration of DHEA, The protective effects of DHEA appear to be specific in that other related steroids and metabolites of DHEA, such as 5-androstene-3 beta, 17 beta-diol, etiocholan-3 alpha-ol-17-one, etiocholan-3 beta-ol-17-one, testosterone, and 5 alpha-androstane-3,17-dione, offered no protection even at 50 mu M concentrations. In addition, using immunocytochemical techniques, we observed that 20 hr of treatment with 5 mM glutamate remarkably increased glucocorticoid receptor (GR) nuclear localization in neuronal cells. Interestingly, 5 mu M DHEA treatment for 24 hr, followed by 5 mM glutamate treatment for 20 hr almost completely reversed the copious nuclear localization of GR observed by glutamate treatment alone. Results obtained suggest that DHEA protects hippocampal neurons, at least in part, by its antiglucocorticoid action via decreasing hippocampal cells nuclear GR levels.
