Carden S E, Hofer M A
Department of Psychiatry, New York State Psychiatric Institute, New York 10032.
Behav Neurosci. 1990 Feb;104(1):160-6. doi: 10.1037//0735-7044.104.1.160.
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.
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。