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水合氯醛诱导的大鼠伏隔核中电刺激多巴胺溢出的变化。

Speedball induced changes in electrically stimulated dopamine overflow in rat nucleus accumbens.

机构信息

Department of Physiology and Pharmacology, Wake Forest University School of Medicine, Winston-Salem, NC 27101, USA.

出版信息

Neuropharmacology. 2011 Feb-Mar;60(2-3):312-7. doi: 10.1016/j.neuropharm.2010.09.014. Epub 2010 Sep 24.

Abstract

Cocaine/heroin combinations (speedball) induce a synergistic elevation in extracellular dopamine concentrations (DA) in the nucleus accumbens (NAc) that can explain the increased abuse liability of speedball. To further delineate the mechanism of this neurochemical synergism, in vivo fast-scan cyclic voltammetry (FSCV) was used to compare NAc DA release and reuptake kinetic parameters following acute administration of cocaine, heroin and speedball in drug-naïve rats. These parameters were extracted from accumbal DA overflow induced by electrical stimulation of the ventral tegmental area. Evoked DA efflux was increased following both cocaine and speedball delivery, whereas heroin did not significantly change evoked DA release from baseline. DA efflux was significantly greater following cocaine compared to speedball. However, DA transporter (DAT) apparent affinity (K(m)) values were similarly elevated following cocaine and speedball administration, but unaffected by heroin. Neither drug induced substantial changes in the maximal reuptake rate (V(max)). These data, combined with published microdialysis and electrophysiological results, indicate that the combination of cocaine-induced competitive inhibition of DAT and the increase in the DA release elicited by heroin is responsible for the synergistic increase in (DA) induced by speedball.

摘要

可卡因/海洛因混合物(快球)在伏隔核(NAc)中诱导细胞外多巴胺浓度([DA](e))的协同升高,这可以解释快球滥用的增加。为了进一步阐明这种神经化学协同作用的机制,在体内使用快速扫描循环伏安法(FSCV)比较了可卡因、海洛因和快球在药物-naïve 大鼠急性给药后对 NAc DA 释放和再摄取动力学参数的影响。这些参数是从腹侧被盖区电刺激诱导的 accumbal DA 溢出中提取的。可卡因和快球给药后,诱发的 DA 外流量增加,而海洛因没有明显改变基线时诱发的 DA 释放。与快球相比,可卡因引起的 DA 外流量显著增加。然而,可卡因和快球给药后,DA 转运体(DAT)的表观亲和力(K(m))值相似升高,但不受海洛因影响。两种药物均未引起最大再摄取速率(V(max))的实质性变化。这些数据结合已发表的微透析和电生理结果表明,可卡因诱导的 DAT 竞争抑制和海洛因引起的 DA 释放增加的组合是快球诱导的[DA](e)协同增加的原因。

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