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苯二氮卓类药物与阿片类药物在抑制幼鼠隔离应激反应中的作用独立性

Independence of benzodiazepine and opiate action in the suppression of isolation distress in rat pups.

作者信息

Carden S E, Hofer M A

机构信息

Department of Psychiatry, New York State Psychiatric Institute, New York 10032.

出版信息

Behav Neurosci. 1990 Feb;104(1):160-6. doi: 10.1037//0735-7044.104.1.160.

Abstract

To determine whether benzodiazepines (BDZs) quiet isolation distress in 10-day-old rat pups by causing a release of endogenous opioids, a blockade of the effects of chlordiazepoxide (CDP) by the opiate antagonist naltrexone (NLX) was sought. Nonsedating doses of morphine (MOR) (0.125 mg/kg) and CDP (2.0 mg/kg) were equally effective in reducing ultrasonic vocalizations and other indices of isolation distress. Appropriate blocking agents NLX, (0.5 mg/kg) against MOR and Ro 15-1788 (4.0 mg/kg) against CDP returned distress measures to levels of saline-treated rat pups. However, NLX failed to reverse the quieting effects of CDP. If CDP potentiates endogenous opioid release, then NLX should block the CDP effect. A higher dose of CDP did not reveal a release of endogenous opioids, and a higher dose of NLX did not antagonize CDP. The quieting effects of BDZs on isolation distress do not appear to be mediated by the opiate system.

摘要

为了确定苯二氮䓬类药物(BDZs)是否通过促使内源性阿片类物质释放来减轻10日龄大鼠幼崽的隔离应激反应,研究人员尝试用阿片拮抗剂纳曲酮(NLX)阻断氯氮䓬(CDP)的作用。非镇静剂量的吗啡(MOR)(0.125毫克/千克)和CDP(2.0毫克/千克)在减少超声发声及其他隔离应激指标方面效果相同。针对MOR的适当阻断剂NLX(0.5毫克/千克)和针对CDP的Ro 15 - 1788(4.0毫克/千克)使应激指标恢复到生理盐水处理的大鼠幼崽的水平。然而,NLX未能逆转CDP的镇静作用。如果CDP增强内源性阿片类物质的释放,那么NLX应该能阻断CDP的作用。更高剂量的CDP并未显示内源性阿片类物质的释放,更高剂量的NLX也未拮抗CDP。BDZs对隔离应激的镇静作用似乎并非由阿片系统介导。

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