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伏隔核中依赖环磷酸腺苷的蛋白激酶A(PKA)活性受到调节后,自我给药可卡因的动机持续变化。

Persistent changes in motivation to self-administer cocaine following modulation of cyclic AMP-dependent protein kinase A (PKA) activity in the nucleus accumbens.

作者信息

Lynch W J, Taylor J R

机构信息

Department of Psychiatry, Yale University School of Medicine, CMHC, Abraham Ribicoff Research Facilities, 34 Park Street, New Haven, CT 06508, USA.

出版信息

Eur J Neurosci. 2005 Sep;22(5):1214-20. doi: 10.1111/j.1460-9568.2005.04305.x.

Abstract

Drug-induced neuroadaptations within the nucleus accumbens, including activation of cAMP-dependent protein kinase A (PKA), may contribute to the synaptic plasticity and behavioural changes that underlie drug addiction. As a direct test of this hypothesis, we examined the effects in rats of PKA activation (Sp-cAMPS infusions of 10 and 20 nmol/side) and inhibition (Rp-cAMPS infusions of 10 and 20 nmol/side) in the nucleus accumbens on motivation to obtain cocaine as measured by responding under the progressive-ratio schedule. Bilateral infusions of Sp-cAMPS (20 nmol/side) resulted in an increase in progressive-ratio responding for cocaine and this effect persisted for several days. In contrast, Rp-cAMPS (20 nmol/side) produced persistent decreases in progressive-ratio responding for cocaine beginning on the day of administration and lasting for several days. These data suggest that alternations in PKA activity within the nucleus accumbens as a consequence of repeated cocaine exposure may contribute to addiction by producing persistent increases in motivation to obtain cocaine.

摘要

伏隔核内的药物诱导神经适应性变化,包括环磷酸腺苷(cAMP)依赖性蛋白激酶A(PKA)的激活,可能导致了作为药物成瘾基础的突触可塑性和行为改变。作为对这一假设的直接验证,我们研究了在伏隔核中激活PKA(双侧注射10和20 nmol/侧的Sp-cAMPS)和抑制PKA(双侧注射10和20 nmol/侧的Rp-cAMPS)对大鼠获取可卡因动机的影响,采用累进比率程序进行测量。双侧注射Sp-cAMPS(20 nmol/侧)导致大鼠对可卡因的累进比率反应增加,且这种效应持续了数天。相反,Rp-cAMPS(20 nmol/侧)从给药当天开始就使大鼠对可卡因的累进比率反应持续下降,并持续数天。这些数据表明,反复接触可卡因导致伏隔核内PKA活性的改变,可能通过持续增加获取可卡因的动机而导致成瘾。

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