Suppr超能文献

脱氢表雄酮对处于十字迷宫中的小鼠具有抗焦虑作用。

Dehydroepiandrosterone is an anxiolytic in mice on the plus maze.

作者信息

Melchior C L, Ritzmann R F

机构信息

Department of Psychiatry, Olive View/UCLA Medical Center, Sylmar 91342.

出版信息

Pharmacol Biochem Behav. 1994 Mar;47(3):437-41. doi: 10.1016/0091-3057(94)90140-6.

Abstract

Dehydroepiandrosterone (DHEA) and its sulfate (DHEAS) are neurosteroids that have been shown to interact with the GABA system. The present study examined the effects of these compounds in mice on motor activity and behavior in the elevated plus maze. Doses of 0.5 mg/kg and above of DHEA reduced motor activity. This effect was blocked by diazepam, RO15-1788, pentylenetetrazole (PTZ), and ethanol. Both DHEA and DHEAS showed anxiolytic activity in the plus maze test, with DHEA being effective over a very wide range of doses (5 micrograms/kg to 1.0 mg/kg). Both RO15-1788 and PTZ blocked the anxiolytic effect of DHEA, there was no interaction with diazepam, and ethanol enhanced the anxiolytic effect of DHEA. At 1.0 mg/kg, DHEAS blocked the anxiolytic effect of ethanol. These results support the hypothesis that neurosteroids could be involved in the termination of a stress response.

摘要

脱氢表雄酮(DHEA)及其硫酸盐(DHEAS)是已被证明可与γ-氨基丁酸(GABA)系统相互作用的神经甾体。本研究检测了这些化合物对小鼠运动活性以及在高架十字迷宫中行为的影响。0.5毫克/千克及以上剂量的DHEA可降低运动活性。这种作用被地西泮、RO15 - 1788、戊四氮(PTZ)和乙醇阻断。在十字迷宫试验中,DHEA和DHEAS均表现出抗焦虑活性,DHEA在非常广泛的剂量范围(5微克/千克至1.0毫克/千克)内均有效。RO15 - 1788和PTZ均阻断了DHEA的抗焦虑作用,与地西泮无相互作用,且乙醇增强了DHEA的抗焦虑作用。在1.0毫克/千克时,DHEAS阻断了乙醇的抗焦虑作用。这些结果支持了神经甾体可能参与应激反应终止的假说。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验