The Orbitofrontal Cortex to Striatal Cholinergic Interneuron Circuit Controls Cognitive Flexibility Shaping Alcohol-Seeking Behavior.

IF 9.6 1区 医学 Q1 NEUROSCIENCES Biological Psychiatry Pub Date : 2024-10-11 DOI:10.1016/j.biopsych.2024.10.005
Jiaxin Li, Yao Zhou, Fangyuan Yin, Yanfeng Du, Jiancheng Xu, Shuyuan Fan, Ziyi Li, Xiaojie Wang, Qingfeng Shen, Yongsheng Zhu, Tengfei Ma
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Abstract

Background: A top-down neuronal circuit from the orbitofrontal cortex (OFC) to the dorsomedial striatum (DMS) appears to be critical for cognitive flexibility. However, how OFC projections to different types of neurons in the DMS control cognitive flexibility and contribute to substance seeking and use, which are relatively inflexible behaviors, remains unclear.

Methods: Mice were trained on two-bottle choice and operant alcohol self-administration procedures. The cognitive flexibility of the mice was tested through a place discrimination task. Electrophysiology and in vivo optogenetics were used to test the function of neural circuits in alcohol-seeking behavior.

Results: We depicted a connection from the OFC to striatal neurons and found that OFC afferents could elicit functional flexibility in striatal cholinergic interneurons (CINs). A mouse model of chronic alcohol consumption showed impaired cognitive flexibility and reduced burst-pause firing. The impairment of the OFC-DMS circuit resulted in a reduction in glutamatergic transmission in OFC-medium spiny neurons (MSNs) through a CIN-mediated pre-inhibition mechanism. Importantly, remodeling the OFC-DMS circuit by inducing LTP restored cognitive flexibility. Furthermore, CINs were responsible for the impact of remodeling of the OFC-DMS circuit on cognitive flexibility. This regulatory role of CINs preferentially facilitated the potentiation of glutamatergic transmission in D2 receptor-expressing medium spiny neurons (D2-MSNs) but not in D1-MSNs. Finally, activation of the OFC-CIN-D2-MSN circuit decreased alcohol-seeking behavior.

Conclusions: Improving OFC-CIN circuit-mediated cognitive flexibility may provide a novel strategy for treating uncontrolled alcohol-seeking behavior.

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轨道额叶皮层到纹状体胆碱能间质环路控制认知灵活性塑造酗酒行为
背景:从眶额皮层(OFC)到背内侧纹状体(DMS)的自上而下的神经元回路似乎对认知灵活性至关重要。然而,OFC对DMS中不同类型神经元的投射是如何控制认知灵活性并导致药物寻求和使用这些相对缺乏灵活性的行为的,目前仍不清楚:方法:对小鼠进行双瓶选择和操作性酒精自我给药程序的训练。方法:对小鼠进行双瓶选择和操作性酒精自我给药训练,并通过位置辨别任务测试小鼠的认知灵活性。电生理学和体内光遗传学被用来测试神经回路在酒精寻求行为中的功能:结果:我们描绘了从OFC到纹状体神经元的连接,并发现OFC传入可诱导纹状体胆碱能中间神经元(CINs)的功能灵活性。长期饮酒的小鼠模型显示认知灵活性受损,爆发-暂停点燃减少。OFC-DMS回路受损导致OFC-中刺神经元(MSN)通过CIN介导的预抑制机制减少了谷氨酸能传导。重要的是,通过诱导 LTP 重塑 OFC-DMS 回路可恢复认知灵活性。此外,CINs是重塑OFC-DMS回路对认知灵活性产生影响的原因。CINs的这种调节作用优先促进了表达D2受体的中刺神经元(D2-MSNs)而非D1-MSNs的谷氨酸能传导的效力。最后,激活OFC-CIN-D2-MSN回路可减少酒精寻求行为:结论:改善OFC-CIN回路介导的认知灵活性可能是治疗失控酗酒行为的一种新策略。
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来源期刊
Biological Psychiatry
Biological Psychiatry 医学-精神病学
CiteScore
18.80
自引率
2.80%
发文量
1398
审稿时长
33 days
期刊介绍: Biological Psychiatry is an official journal of the Society of Biological Psychiatry and was established in 1969. It is the first journal in the Biological Psychiatry family, which also includes Biological Psychiatry: Cognitive Neuroscience and Neuroimaging and Biological Psychiatry: Global Open Science. The Society's main goal is to promote excellence in scientific research and education in the fields related to the nature, causes, mechanisms, and treatments of disorders pertaining to thought, emotion, and behavior. To fulfill this mission, Biological Psychiatry publishes peer-reviewed, rapid-publication articles that present new findings from original basic, translational, and clinical mechanistic research, ultimately advancing our understanding of psychiatric disorders and their treatment. The journal also encourages the submission of reviews and commentaries on current research and topics of interest.
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