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

机译:用于奖励救济的自上而下神经机制的分子与电路动态识别

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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 sub-population of these top-down projecting neurons, identified by 2-photon Ca2+ 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 micro-circuit-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.
机译:寻求奖励行为是生存的基础,但抑制这种行为也是必不可少的,即使对于高价值的奖励。在人类和啮齿动物中,内侧前额定皮层(MPFC)涉及抑制奖励求取;然而,尽管在健康和疾病方面具有至关重要的意义,但MPFC调节奖励寻求的神经电路仍然不完全了解。在这里,我们表明,对核心腺(NAC)神经元的子场(NAC)神经元的特定子集自然地编码决定在面对惩罚风险时启动或抑制奖励寻求。发现由2-光子CA2 +成像和活性依赖性标记鉴定的这些自上而下的突出突出神经元的高度分辨的亚群,发现能够抑制奖励寻求。这种自然活动解决的MPFC-to-NAC投影显示了独特的分子遗传和微型电路级别的特征,在寻求奖励行为的调节中具有守恒作用,提供了行为和可能的治疗意义的细胞和解剖学标识。

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