Ro 15-4513 alteration of pentobarbital dependence

被引:1
|
作者
Yutrzenka, GJ
Stone, T
Anderson, S
机构
[1] Dept. of Physiology and Pharmacology, School of Medicine, University of South Dakota, Vermillion, SD 57069
关键词
inverse agonists; dependence; pentobarbital; Ro; 15-4513; rats;
D O I
10.1016/S0091-3057(96)00107-4
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
This study investigated the ability of the benzodiazepine inverse agonist, Ro 15-4513, to alter the expression of physical dependence on pentobarbital. Male Sprague-Dawley rats were made physically dependent on pentobarbital by continuous, IP, infusion of escalating doses of pentobarbital for 12 days. In Experiment 1, pentobarbital dependent rats received either vehicle or Ro 15-4513, in doses of 5, 10, or 15 mg/kg, IF, periodically during the pentobarbital abstinence period. As expected, Ro 15-4513 produced a significant. dose-dependent, exacerbation of withdrawal signs in the pentobarbital dependent rats. In Experiment 2, either vehicle or Ro 15-4513, at a dose of 15 mg/kg, was administered, IF, once daily during the 12 days of continuous pentobarbital infusion. During the subsequent pentobarbital abstinence period it was noted that the withdrawal signs were significantly reduced in the rats receiving the daily administration of Ro 15-4513. It is hypothesized that the benzodiazepine inverse agonist, Ro 15-4513, may inhibit the development of physical dependence on pentobarbital through an opposing action on the GABA-A receptor. Copyright (C) 1996 Elsevier Science Inc.
引用
收藏
页码:379 / 386
页数:8
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