光遗传学
伏隔核
前额叶皮质
神经科学
被盖腹侧区
多巴胺
兴奋性突触后电位
索马
心理学
生物
认知
多巴胺能
抑制性突触后电位
作者
Bo Xing,Nancy R. Mack,Kaiming Guo,Yu-Xiang Zhang,Billy Ramirez,Sha-Sha Yang,Li Lin,Dong V. Wang,Yanchun Li,Wen‐Jun Gao
标识
DOI:10.1016/j.biopsych.2020.08.023
摘要
The medial prefrontal cortex (mPFC) is essential for social behaviors, yet whether and how it encodes social memory remains unclear.We combined whole-cell patch recording, morphological analysis, optogenetic/chemogenetic manipulation, and the TRAP (targeted recombination in active populations) transgenic mouse tool to study the social-associated neural populations in the mPFC.Fos-TRAPed prefrontal social-associated neurons are excitatory pyramidal neurons with relatively small soma sizes and thin-tufted apical dendrite. These cells exhibit intrinsic firing features of dopamine D1 receptor-like neurons, show persisting firing pattern after social investigation, and project dense axons to nucleus accumbens. In behaving TRAP mice, selective inhibition of prefrontal social-associated neurons does not affect social investigation but does impair subsequent social recognition, whereas optogenetic reactivation of their projections to the nucleus accumbens enables recall of a previously encountered but "forgotten" mouse. Moreover, chemogenetic activation of mPFC-to-nucleus accumbens projections ameliorates MK-801-induced social memory impairments.Our results characterize the electrophysiological and morphological features of social-associated neurons in the mPFC and indicate that these Fos-labeled, social-activated prefrontal neurons are necessary and sufficient for social memory.
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