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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >A role for nucleus accumbens glutamate transmission in the relapse to cocaine-seeking behavior.
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A role for nucleus accumbens glutamate transmission in the relapse to cocaine-seeking behavior.

机译:伏隔核谷氨酸传递在可卡因寻求行为复发中的作用。

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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.
机译:这项研究调查了向伏隔核中施用离子型谷氨酸受体激动剂或拮抗剂对维持可卡因自我给药和恢复可卡因寻求行为的影响。用α-氨基-3-羟基-5-甲基异恶唑-4-丙酸对伏隔核中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的刺激酸或1-氨基环丁烷-顺式1,3-二羧酸分别减少了可卡因增强的反应次数,表明可卡因的奖励作用增强。相反,用N-甲基-D-天冬氨酸盐阻断α-氨基-3-羟基-5-甲基异恶唑-4-丙酸受体,或用马来酸地佐西平或2-氨基-5-甲基苯磺酸阻断N-甲基-D-天冬氨酸受体。磷酸新戊酸对维持可卡因自我给药没有选择性作用。从药物配对杠杆的增强提示中消失了一个星期后,细胞核中的α-氨基-3-羟基-5-甲基异恶唑-4-丙酸和1-氨基环丁烷-顺1,3-二羧酸均被处理。伏安族恢复了可卡因寻找行为。但是,α-氨基-3-羟基-5-甲基异恶唑-4-丙酸处理仅对药物配对的杠杆增加响应,而1-氨基环丁烷-顺式1,3-二羧酸对两种药物配对的响应均增加。和非毒品配对杠杆。这些结果表明刺激伏隔核中的谷氨酸受体增强了可卡因的增强作用,但是维持可卡因自我给药不需要谷氨酸的传播。另外,增加伏隔核中谷氨酸的传递可能与促进可卡因寻找行为的复发有关。

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