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γ-丁内酯对可卡因释放机制的体内伏安法研究。

In vivo voltammetric studies on release mechanisms for cocaine with gamma-butyrolactone.

作者信息

Broderick P A

机构信息

Department of Pharmacology, City University of New York Medical School, NY.

出版信息

Pharmacol Biochem Behav. 1991 Dec;40(4):969-75. doi: 10.1016/0091-3057(91)90113-g.

Abstract

The effect of cocaine (20 mg/kg SC) on presynaptic mechanisms of release for dopamine (DA) and for serotonin (5-HT) was studied in nucleus accumbens of unrestrained rats (Rattus norvegicus). The studies were done by assaying synaptic concentrations of DA and 5-HT in the presence of the neuronal impulse flow inhibitor, gamma-butyrolactone (gamma-BL). The results were compared with cocaine effects on accumbens DA and 5-HT in the freely moving rat, without gamma-BL treatment. A neurochemical time course profile showed that the cocaine-induced increase in accumbens synaptic concentrations of DA was significantly blocked (p less than 0.0001) after DA impulse flow was significantly inhibited (p less than 0.0038) by gamma-BL (35.8%). The neurochemical time course profile concurrently showed that the cocaine-induced decrease in accumbens synaptic concentrations of 5-HT was significantly blocked (p less than 0.0004) after impulse flow was significantly inhibited (p less than 0.025) by gamma-BL (50.6%). The findings show that cocaine's effects on synaptic concentrations for DA and for 5-HT in accumbens are dependent on neuronal impulse flow. The findings indicate that presynaptic releasing mechanisms, which may be different for DA vis-à-vis 5-HT, play a role in the mechanism of action of cocaine.

摘要

研究了可卡因(20毫克/千克,皮下注射)对自由活动大鼠伏隔核中多巴胺(DA)和5-羟色胺(5-HT)突触前释放机制的影响。研究通过在存在神经元冲动流抑制剂γ-丁内酯(γ-BL)的情况下测定DA和5-HT的突触浓度来进行。将结果与可卡因对未接受γ-BL处理的自由活动大鼠伏隔核中DA和5-HT的影响进行比较。神经化学时间进程曲线显示,在γ-BL(35.8%)显著抑制DA冲动流(p<0.0038)后,可卡因诱导的伏隔核中DA突触浓度增加被显著阻断(p<0.0001)。神经化学时间进程曲线同时显示,在γ-BL(50.6%)显著抑制冲动流(p<0.025)后,可卡因诱导的伏隔核中5-HT突触浓度降低被显著阻断(p<0.0004)。这些发现表明,可卡因对伏隔核中DA和5-HT突触浓度的影响取决于神经元冲动流。这些发现表明,对于DA和5-HT而言可能不同的突触前释放机制在可卡因的作用机制中发挥作用。

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