DIFFERENTIAL REDUCTION OF MORPHINE-WITHDRAWAL BODY SHAKES BY BUTACLAMOL ENANTIOMERS

被引:14
作者
HYNES, MD
MCCARTEN, MD
SHEARMAN, G
LAL, H
机构
[1] Department of Pharmacology, Toxicology College, Pharmacy University of Rhode Island, Kingston
关键词
D O I
10.1016/0024-3205(78)90421-6
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Rats withdrawn from continuous morphine infusion showed reliable occurrence of withdrawal body shakes. This sign of narcotic withdrawal was inhibited by the neuroleptic drug, (+) butaclamol. (-) Butaclamol was inactive. (+) Butaclamol activity was not antagonized by naloxone (5 mg/kg). The anti-withdrawal mechanism of (+) butaclamol is discussed in terms of effects on dopamine and narcotic receptors. The butyrophenone neuroleptic, haloperidol, has been used successfully to reduce signs of narcotic withdrawal in laboratory animals (1-4) and human addicts (5). Other neuroleptics of the butyrophenone type also show anti-withdrawal action (6, 7). The mechanism of action of these neuroleptics in blocking narcotic withdrawal is not understood. Butaclamol is a new neuroleptic drug that is available in two enantiomers and only (+) butaclamol possesses neuroleptic activity (8-10). Because of its demonstrated stereo-specificity in producing its pharmacological action, we employed this drug to establish specificity of action of neuroleptics in blocking narcotic withdrawal. © 1978.
引用
收藏
页码:133 / 136
页数:4
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