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M4 毒蕈碱型乙酰胆碱受体基因敲除小鼠可卡因自我给药增加。

Increased cocaine self-administration in M4 muscarinic acetylcholine receptor knockout mice.

机构信息

Laboratory of Neuropsychiatry, Rigshospitalet University Hospital, Copenhagen, Denmark.

出版信息

Psychopharmacology (Berl). 2011 Aug;216(3):367-78. doi: 10.1007/s00213-011-2225-4. Epub 2011 Mar 5.

Abstract

RATIONALE

The reinforcing effects of cocaine are mediated by the mesolimbic dopamine system. Behavioral and neurochemical studies have shown that the cholinergic muscarinic M(4) receptor subtype plays an important role in regulation of dopaminergic neurotransmission.

OBJECTIVES

Here we investigated for the first time the involvement of M(4) receptors in the reinforcing effects of cocaine using chronic intravenous cocaine self-administration in extensively backcrossed M(4) receptor knockout (M(4) (-/-)) mice.

METHODS

We evaluated acquisition of cocaine self-administration in experimentally naïve mice. Both cocaine self-administration and food-maintained operant behavior were evaluated under fixed ratio 1 (FR 1) and progressive ratio (PR) schedules of reinforcement. In addition, cocaine-induced dopamine release and cocaine-induced hyperactivity were evaluated.

RESULTS

M(4) (-/-) mice earned significantly more cocaine reinforcers and reached higher breaking points than their wild-type littermates (M(4) (+/+)) at intermediate doses of cocaine under both FR 1 and PR schedules of reinforcement. Under the PR schedule, M(4) (-/-) mice exhibited significantly higher response rates at the lowest liquid food concentration. In accordance with these results, cocaine-induced dopamine efflux in the nucleus accumbens and hyperlocomotion were increased in M(4) (-/-) mice compared to M(4) (+/+) mice.

CONCLUSIONS

Our data suggest that M(4) receptors play an important role in regulation of the reward circuitry and may serve as a new target in the medical treatment of drug addiction.

摘要

原理

可卡因的强化作用是通过中脑边缘多巴胺系统介导的。行为和神经化学研究表明,胆碱能毒蕈碱 M(4)受体亚型在调节多巴胺能神经传递中发挥重要作用。

目的

本研究首次使用广泛回交的 M(4) 受体敲除 (M(4) (-/-)) 小鼠,通过慢性静脉内可卡因自我给药,研究 M(4) 受体在可卡因强化作用中的作用。

方法

我们评估了实验性新生小鼠对可卡因的自我给药情况。在固定比率 1 (FR 1) 和逐步比率 (PR) 强化方案下,评估可卡因自我给药和食物维持操作性行为。此外,还评估了可卡因诱导的多巴胺释放和可卡因诱导的过度活动。

结果

M(4) (-/-) 小鼠在 FR 1 和 PR 强化方案下,在中等剂量的可卡因下,与野生型同窝小鼠 (M(4) (+/+)) 相比,获得了显著更多的可卡因奖励,并达到了更高的突破点。在 PR 方案下,M(4) (-/-) 小鼠在最低的液体食物浓度下表现出显著更高的反应率。与这些结果一致,与 M(4) (+/+) 小鼠相比,M(4) (-/-) 小鼠的伏隔核中可卡因诱导的多巴胺外排和过度活动增加。

结论

我们的数据表明,M(4) 受体在调节奖励回路中发挥重要作用,可能成为治疗药物成瘾的新靶点。

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