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向内侧视前区微量注射三唑仑催眠作用的特征

Characterization of the hypnotic effects of triazolam microinjections into the medial preoptic area.

作者信息

Mendelson W B, Martin J V

机构信息

Dept. of Psychiatry, State University of New York, Stony Brook 11794-8101.

出版信息

Life Sci. 1992;50(15):1117-28. doi: 10.1016/0024-3205(92)90349-t.

Abstract

We have previously reported that microinjections of the benzodiazepine hypnotic triazolam into the medial preoptic area (MPA) of the hypothalamus enhance sleep in rats. The present study further characterizes this effect, by examining its anatomical specificity, determining whether it is mediated by interaction with central benzodiazepine receptors, and assessing whether sleep induction is associated with changes in core temperature. It was found that microinjections of 0.25 and 0.5 micrograms triazolam into two nearby structures, the lateral preoptic area and diagonal band of Broca, failed to alter sleep. Total sleep time was enhanced by microinjection of triazolam into the MPA, and this effect was blocked by co-administration of the benzodiazepine receptor blocker RO 15-1788. Sleep enhancement by triazolam was not associated with significant alterations in core body temperature. These observations continue to suggest that the MPA may be a site which mediates the hypnotic effect of triazolam, and add to the growing body of data emphasizing the importance of hypothalamic function in the regulation of sleep and waking.

摘要

我们之前曾报道,向下丘脑的内侧视前区(MPA)微量注射苯二氮䓬类催眠药三唑仑可增强大鼠的睡眠。本研究通过检查其解剖学特异性、确定其是否通过与中枢苯二氮䓬受体相互作用介导以及评估睡眠诱导是否与核心体温变化相关,进一步对这种效应进行了表征。结果发现,向两个相邻结构,即外侧视前区和布罗卡斜带微量注射0.25微克和0.5微克三唑仑,未能改变睡眠。向MPA微量注射三唑仑可增加总睡眠时间,并且这种效应被苯二氮䓬受体阻滞剂RO 15 - 1788共同给药所阻断。三唑仑增强睡眠与核心体温的显著变化无关。这些观察结果继续表明,MPA可能是介导三唑仑催眠作用的部位,并增加了越来越多强调下丘脑功能在睡眠和觉醒调节中重要性的数据。

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