Ventral pallidal regulation of motivated behaviors and reinforcement.

IF 3.4 3区 医学 Q2 NEUROSCIENCES Frontiers in Neural Circuits Pub Date : 2023-02-02 eCollection Date: 2023-01-01 DOI:10.3389/fncir.2023.1086053
Carina Soares-Cunha, Jasper A Heinsbroek
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Abstract

The interconnected nuclei of the ventral basal ganglia have long been identified as key regulators of motivated behavior, and dysfunction of this circuit is strongly implicated in mood and substance use disorders. The ventral pallidum (VP) is a central node of the ventral basal ganglia, and recent studies have revealed complex VP cellular heterogeneity and cell- and circuit-specific regulation of reward, aversion, motivation, and drug-seeking behaviors. Although the VP is canonically considered a relay and output structure for this circuit, emerging data indicate that the VP is a central hub in an extensive network for reward processing and the regulation of motivation that extends beyond classically defined basal ganglia borders. VP neurons respond temporally faster and show more advanced reward coding and prediction error processing than neurons in the upstream nucleus accumbens, and regulate the activity of the ventral mesencephalon dopamine system. This review will summarize recent findings in the literature and provide an update on the complex cellular heterogeneity and cell- and circuit-specific regulation of motivated behaviors and reinforcement by the VP with a specific focus on mood and substance use disorders. In addition, we will discuss mechanisms by which stress and drug exposure alter the functioning of the VP and produce susceptibility to neuropsychiatric disorders. Lastly, we will outline unanswered questions and identify future directions for studies necessary to further clarify the central role of VP neurons in the regulation of motivated behaviors. Significance: Research in the last decade has revealed a complex cell- and circuit-specific role for the VP in reward processing and the regulation of motivated behaviors. Novel insights obtained using cell- and circuit-specific interrogation strategies have led to a major shift in our understanding of this region. Here, we provide a comprehensive review of the VP in which we integrate novel findings with the existing literature and highlight the emerging role of the VP as a linchpin of the neural systems that regulate motivation, reward, and aversion. In addition, we discuss the dysfunction of the VP in animal models of neuropsychiatric disorders.

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腹侧苍白球对动机行为的调节和强化。
腹侧基底神经节相互连接的细胞核长期以来一直被认为是动机行为的关键调节因子,而这种回路的功能障碍与情绪和物质使用障碍密切相关。腹侧苍白球(VP)是腹侧基底神经节的中心节点,最近的研究揭示了复杂的VP细胞异质性以及奖赏、厌恶、动机和药物寻求行为的细胞和回路特异性调节。尽管VP通常被认为是该电路的中继和输出结构,但新出现的数据表明,VP是广泛的奖励处理和动机调节网络中的中心枢纽,该网络延伸到经典定义的基底神经节边界之外。与上游伏隔核的神经元相比,VP神经元在时间上反应更快,表现出更先进的奖励编码和预测错误处理,并调节腹侧中脑多巴胺系统的活性。这篇综述将总结文献中的最新发现,并提供关于复杂的细胞异质性以及细胞和电路对动机行为的特异性调节和VP的强化的最新信息,特别关注情绪和物质使用障碍。此外,我们将讨论压力和药物暴露改变VP功能并产生神经精神障碍易感性的机制。最后,我们将概述尚未回答的问题,并确定未来的研究方向,以进一步阐明VP神经元在动机行为调节中的核心作用。意义:过去十年的研究揭示了VP在奖励处理和动机行为调节中复杂的细胞和电路特异性作用。使用细胞和电路特异性询问策略获得的新见解导致我们对该区域的理解发生了重大转变。在这里,我们对VP进行了全面的综述,其中我们将新的发现与现有文献相结合,并强调了VP作为调节动机、奖励和厌恶的神经系统的关键的新兴作用。此外,我们还讨论了VP在神经精神障碍动物模型中的功能障碍。
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来源期刊
CiteScore
6.00
自引率
5.70%
发文量
135
审稿时长
4-8 weeks
期刊介绍: Frontiers in Neural Circuits publishes rigorously peer-reviewed research on the emergent properties of neural circuits - the elementary modules of the brain. Specialty Chief Editors Takao K. Hensch and Edward Ruthazer at Harvard University and McGill University respectively, are supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics and the public worldwide. Frontiers in Neural Circuits launched in 2011 with great success and remains a "central watering hole" for research in neural circuits, serving the community worldwide to share data, ideas and inspiration. Articles revealing the anatomy, physiology, development or function of any neural circuitry in any species (from sponges to humans) are welcome. Our common thread seeks the computational strategies used by different circuits to link their structure with function (perceptual, motor, or internal), the general rules by which they operate, and how their particular designs lead to the emergence of complex properties and behaviors. Submissions focused on synaptic, cellular and connectivity principles in neural microcircuits using multidisciplinary approaches, especially newer molecular, developmental and genetic tools, are encouraged. Studies with an evolutionary perspective to better understand how circuit design and capabilities evolved to produce progressively more complex properties and behaviors are especially welcome. The journal is further interested in research revealing how plasticity shapes the structural and functional architecture of neural circuits.
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