Sun Qingtao, Liu Mingzhe, Guan Wuqiang, Xiao Xiong, Dong Chunyang, Bruchas Michael R, Zweifel Larry S, Li Yulong, Tian Lin, Li Bo
bioRxiv. 2024 Jul 31:2024.07.31.605785. doi: 10.1101/2024.07.31.605785.
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 motivational drive in mice. On one hand, dynorphin acts postsynaptically via KORs on local GABAergic neurons in the VP to promote disinhibition of cholinergic neurons, which release acetylcholine into the amygdala to invigorate reward-seeking behaviors. 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 modulate motivation through cholinergic system, and provides an explanation for why these neuromodulators are involved in motivational disorders, including depression and addiction.
内源性阿片肽强啡肽及其受体κ-阿片受体(KOR)与多种不同行为有关,但其潜在机制仍不清楚。我们在此表明,伏隔核强啡肽能神经元释放的强啡肽对腹侧苍白球(VP)去抑制性回路发挥强大调节作用,从而控制小鼠向杏仁核的胆碱能传递及动机驱力。一方面,强啡肽通过VP中局部GABA能神经元上的KOR在突触后发挥作用,促进对胆碱能神经元的去抑制,胆碱能神经元向杏仁核释放乙酰胆碱以激发奖赏寻求行为。另一方面,强啡肽还通过强啡肽能终末上的KOR在突触前发挥作用,限制其自身释放。这种自身抑制可防止胆碱能神经元长时间激活和乙酰胆碱释放,从而防止奖赏寻求行为的持续。我们的研究揭示了强啡肽如何通过胆碱能系统精确调节动机,并解释了为何这些神经调质会参与包括抑郁症和成瘾在内的动机障碍。