Dynorphin modulates reward-seeking actions through a pallido-amygdala cholinergic circuit.

IF 14.7 1区 医学 Q1 NEUROSCIENCES
Neuron Pub Date : 2025-06-04 Epub Date: 2025-04-15 DOI:10.1016/j.neuron.2025.03.018
Qingtao Sun, Mingzhe Liu, Wuqiang Guan, Xiong Xiao, Chunyang Dong, Michael R Bruchas, Larry S Zweifel, Yulong Li, Lin Tian, Bo Li
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引用次数: 0

Abstract

The endogenous opioid peptide dynorphin and its receptor κ-opioid receptor (KOR) have been implicated in divergent behaviors, but the underlying mechanisms remain elusive. Here, we show that dynorphin released from nucleus accumbens dynorphinergic neurons exerts powerful modulation over a ventral pallidum (VP) disinhibitory circuit, thereby controlling cholinergic transmission to the amygdala and reward-seeking behavior in mice. On one hand, dynorphin acts postsynaptically via KORs on VP GABAergic neurons to promote disinhibition of cholinergic neurons, which release acetylcholine into the amygdala to facilitate learning and invigorate actions. On the other hand, dynorphin also acts presynaptically via KORs on dynorphinergic terminals to limit its own release. Such autoinhibition keeps cholinergic neurons from prolonged activation and release of acetylcholine and prevents perseverant reward seeking. Our study reveals how dynorphin exquisitely modulates behavior through the cholinergic system and provides an explanation for why these neuromodulators are involved in motivational disorders, including depression and addiction.

Dynorphin通过苍白体-杏仁核胆碱能回路调节寻求奖励的行为。
内源性阿片肽dynorphin及其受体κ-阿片受体(KOR)参与了不同的行为,但其潜在机制尚不清楚。本研究表明,从伏隔核失啡能神经元释放的失啡肽对腹侧pallidum (VP)去抑制回路施加强大的调节作用,从而控制小鼠向杏仁核的胆碱能传递和寻求奖励的行为。一方面,dynorphin通过KORs突触后作用于VP gaba能神经元,促进胆碱能神经元解除抑制,释放乙酰胆碱到杏仁核,促进学习和激活动作。另一方面,dynorphin也通过KORs作用于突触前的dynorphin能末端,以限制其自身的释放。这种自抑制使胆碱能神经元不能长时间激活和释放乙酰胆碱,并阻止持久的奖赏寻求。我们的研究揭示了动啡如何通过胆碱能系统精细地调节行为,并解释了为什么这些神经调节剂参与动机障碍,包括抑郁和成瘾。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Neuron
Neuron 医学-神经科学
CiteScore
24.50
自引率
3.10%
发文量
382
审稿时长
1 months
期刊介绍: Established as a highly influential journal in neuroscience, Neuron is widely relied upon in the field. The editors adopt interdisciplinary strategies, integrating biophysical, cellular, developmental, and molecular approaches alongside a systems approach to sensory, motor, and higher-order cognitive functions. Serving as a premier intellectual forum, Neuron holds a prominent position in the entire neuroscience community.
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