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

被引:107
作者
Kim, Christina K. [1 ]
Ye, Li [2 ,3 ]
Jennings, Joshua H. [4 ]
Pichamoorthy, Nandini [4 ]
Tang, Daniel D. [4 ]
Yoo, Ai-Chi W. [4 ]
Ramakrishnan, Charu [4 ]
Deisseroth, Karl [2 ,3 ,4 ]
机构
[1] Stanford Univ, Neurosci Program, Stanford, CA 94305 USA
[2] Stanford Univ, HHMI, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Psychiat, Stanford, CA 94305 USA
[4] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
关键词
DEEP BRAIN-STIMULATION; PREFRONTAL CORTEX; BASOLATERAL AMYGDALA; SELECTIVE INACTIVATION; INDUCED REINSTATEMENT; GLUTAMATERGIC INPUTS; DECISION-MAKING; DRIVE AVERSION; NEURONS; PROJECTIONS;
D O I
10.1016/j.cell.2017.07.020
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:1013 / +
页数:29
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