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M5毒蕈碱受体对于多巴胺能神经元的缓慢激活以及对大脑刺激的奖赏作用是必需的。

M5 muscarinic receptors are needed for slow activation of dopamine neurons and for rewarding brain stimulation.

作者信息

Yeomans J, Forster G, Blaha C

机构信息

Department of Psychology, University of Toronto, Ontario, Canada.

出版信息

Life Sci. 2001 Apr 27;68(22-23):2449-56. doi: 10.1016/s0024-3205(01)01038-4.

Abstract

Mesopontine cholinergic neurons (Ch5 and Ch6 cell groups) activate the cerebral cortex via thalamic projections, and activate locomotion and reward via dopamine neurons in the substantia nigra and ventral tegmental area (VTA). Nicotinic receptors in VTA activate dopamine neurons quickly, and are needed for the stimulant and rewarding effects of nicotine in rats. Muscarinic receptors in VTA activate dopamine neurons slowly, and are needed for the rewarding effects of hypothalamic stimulation, but do not increase locomotion. Antisense oligonucleotides targetting M5 mRNA, when infused into the VTA, inhibited M5 receptor binding and rewarding hypothalamic stimulation. Mutant mice with truncated M5 muscarinic receptor genes drank more water than wild-type controls. Spontaneous locomotion and locomotor responses to amphetamine and scopolamine were unchanged. Electrical stimulation near Ch6 induced dopamine release in the nucleus accumbens in two phases, an early phase (0-2 min after stimulation) dependent on nicotinic and gluatamatergic receptors in VTA, and a late phase (8-50 min after stimulation) dependent on muscarinic receptors in VTA. The late phase was lost in M5 mutant mice, while the early phase was unchanged. M5 muscarinic receptors bind slowly to muscarinic ligands, and appear to mediate slow secretions.

摘要

脑桥中胆碱能神经元(Ch5和Ch6细胞群)通过丘脑投射激活大脑皮层,并通过黑质和腹侧被盖区(VTA)中的多巴胺能神经元激活运动和奖赏。VTA中的烟碱型受体快速激活多巴胺能神经元,是尼古丁对大鼠产生刺激和奖赏作用所必需的。VTA中的毒蕈碱型受体缓慢激活多巴胺能神经元,是下丘脑刺激产生奖赏作用所必需的,但不会增加运动。将靶向M5 mRNA的反义寡核苷酸注入VTA时,可抑制M5受体结合以及下丘脑刺激产生的奖赏作用。M5毒蕈碱型受体基因截短的突变小鼠比野生型对照喝更多的水。对苯丙胺和东莨菪碱的自发运动和运动反应未发生改变。Ch6附近的电刺激在伏隔核中诱导多巴胺释放分两个阶段,早期阶段(刺激后0 - 2分钟)依赖于VTA中的烟碱型和谷氨酸能受体,晚期阶段(刺激后8 - 50分钟)依赖于VTA中的毒蕈碱型受体。晚期阶段在M5突变小鼠中消失,而早期阶段未改变。M5毒蕈碱型受体与毒蕈碱配体结合缓慢,似乎介导缓慢分泌。

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