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抑制奖赏寻求的自上而下神经机制的分子与回路动力学鉴定

Molecular and Circuit-Dynamical Identification of Top-Down Neural Mechanisms for Restraint of Reward Seeking.

作者信息

Kim Christina K, Ye Li, Jennings Joshua H, Pichamoorthy Nandini, Tang Daniel D, Yoo Ai-Chi W, Ramakrishnan Charu, Deisseroth Karl

机构信息

Neurosciences Program, Stanford University, Stanford, CA, 94305, USA.

HHMI, Stanford University, Stanford, CA, 94305, USA; Department of Psychiatry, Stanford University, Stanford, CA, 94305, USA.

出版信息

Cell. 2017 Aug 24;170(5):1013-1027.e14. doi: 10.1016/j.cell.2017.07.020. Epub 2017 Aug 17.

Abstract

Reward-seeking behavior is fundamental to survival, but suppression of this behavior can be essential as well, even for rewards of high value. In humans and rodents, the medial prefrontal cortex (mPFC) has been implicated in suppressing reward seeking; however, despite vital significance in health and disease, the neural circuitry through which mPFC regulates reward seeking remains incompletely understood. Here, we show that a specific subset of superficial mPFC projections to a subfield of nucleus accumbens (NAc) neurons naturally encodes the decision to initiate or suppress reward seeking when faced with risk of punishment. A highly resolved subpopulation of these top-down projecting neurons, identified by 2-photon Ca imaging and activity-dependent labeling to recruit the relevant neurons, was found capable of suppressing reward seeking. This natural activity-resolved mPFC-to-NAc projection displayed unique molecular-genetic and microcircuit-level features concordant with a conserved role in the regulation of reward-seeking behavior, providing cellular and anatomical identifiers of behavioral and possible therapeutic significance.

摘要

寻求奖励行为是生存的基础,但抑制这种行为也可能至关重要,即使是对于高价值的奖励。在人类和啮齿动物中,内侧前额叶皮质(mPFC)与抑制寻求奖励行为有关;然而,尽管其在健康和疾病中具有至关重要的意义,但mPFC调节寻求奖励行为的神经回路仍未被完全理解。在这里,我们表明,mPFC向伏隔核(NAc)神经元一个子领域的特定浅层投射子集,在面临惩罚风险时,自然地编码了启动或抑制寻求奖励的决定。通过双光子钙成像和活动依赖标记鉴定出的这些自上而下投射神经元的一个高度解析的亚群,被发现能够抑制寻求奖励行为。这种自然活动解析的mPFC到NAc的投射表现出独特的分子遗传学和微电路水平特征,与在调节寻求奖励行为中的保守作用一致,提供了行为和可能具有治疗意义的细胞和解剖学标识。

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