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伏隔核谷氨酸传递在可卡因寻求行为复发中的作用。

A role for nucleus accumbens glutamate transmission in the relapse to cocaine-seeking behavior.

作者信息

Cornish J L, Duffy P, Kalivas P W

机构信息

Alcohol and Drug Abuse Program, Washington State University, Pullman, USA.

出版信息

Neuroscience. 1999;93(4):1359-67. doi: 10.1016/s0306-4522(99)00214-6.

Abstract

This study investigated the effect of ionotropic glutamate receptor agonist or antagonist administration into the nucleus accumbens on the maintenance of cocaine self-administration and the reinstatement of cocaine-seeking behavior. The stimulation of alpha-amino-3-hydroxy-5-methylisoxazole-4-proprionic acid or N-methyl-D-aspartate glutamate receptors in the nucleus accumbens with either alpha-amino-3-hydroxy-5-methylisoxazole-4-proprionic acid or 1-aminocyclobutane-cis-1,3-dicarboxylic acid, respectively, decreased the number of cocaine-reinforced responses, suggesting an enhancement in the rewarding properties of cocaine. In contrast, blockade of alpha-amino-3-hydroxy-5-methylisoxazole-4-proprionic acid receptors with N-methyl-D-aspartate, or N-methyl-D-aspartate receptors with dizocilpine maleate or 2-amino-5-phosphonovaleric acid had no selective effect on the maintenance of cocaine self-administration. Following one week of extinction from the reinforcing cue of the drug-paired lever, both alpha-amino-3-hydroxy-5-methylisoxazole-4-proprionic acid and 1-aminocyclobutane-cis-1,3-dicarboxylic acid treatment in the nucleus accumbens reinstated cocaine-seeking behavior. However, alpha-amino-3-hydroxy-5-methylisoxazole-4-proprionic acid treatment increased responding only on the drug-paired lever, while 1-aminocyclobutane-cis-1,3-dicarboxylic acid increased responding on both the drug-paired and non-drug-paired levers. These results suggest that stimulation of glutamate receptors in the nucleus accumbens augments the reinforcing effect of cocaine, yet glutamate transmission is not required to maintain cocaine self-administration. In addition, increased glutamate transmission in the nucleus accumbens may be involved in facilitating the relapse to cocaine-seeking behavior.

摘要

本研究调查了向伏隔核注射离子型谷氨酸受体激动剂或拮抗剂对可卡因自我给药维持及觅药行为恢复的影响。分别用α-氨基-3-羟基-5-甲基异恶唑-4-丙酸或1-氨基环丁烷-顺-1,3-二羧酸刺激伏隔核中的α-氨基-3-羟基-5-甲基异恶唑-4-丙酸或N-甲基-D-天冬氨酸谷氨酸受体,可减少可卡因强化反应的次数,提示可卡因的奖赏特性增强。相比之下,用N-甲基-D-天冬氨酸阻断α-氨基-3-羟基-5-甲基异恶唑-4-丙酸受体,或用马来酸二氮卓或2-氨基-5-磷酸戊酸阻断N-甲基-D-天冬氨酸受体,对可卡因自我给药的维持没有选择性影响。在与药物配对的杠杆的强化线索消退一周后,伏隔核中α-氨基-3-羟基-5-甲基异恶唑-4-丙酸和1-氨基环丁烷-顺-1,3-二羧酸处理均恢复了觅药行为。然而,α-氨基-3-羟基-5-甲基异恶唑-4-丙酸处理仅增加了对与药物配对杠杆的反应,而1-氨基环丁烷-顺-1,3-二羧酸增加了对与药物配对和未与药物配对杠杆的反应。这些结果表明,刺激伏隔核中的谷氨酸受体会增强可卡因的强化作用,但维持可卡因自我给药并不需要谷氨酸传递。此外,伏隔核中谷氨酸传递增加可能参与促进复吸到觅药行为。

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