4.8 Article

Excitatory SST neurons in the medial paralemniscal nucleus control repetitive self and encode reward

期刊

NEURON
卷 110, 期 20, 页码 3356-+

出版社

CELL PRESS
DOI: 10.1016/j.neuron.2022.08.010

关键词

repetitive behavior -related neurons

资金

  1. Ministry of Science and Technology of the People's Republic of China [2021ZD0202800/01]
  2. Natural Science Foundation of China [32070957]
  3. innovative research teams of high-level local universities in Shanghai [SHSMUZDCX20211100, SHSMU-ZDCX20211102]

向作者/读者索取更多资源

The study investigates the neurobiological mechanism of repetitive behaviors in mice and identifies the role of MPLSST neurons in self-grooming and anxiety regulation. Activation of MPLSST neurons promotes rewarding effects and activates dopamine neurons, while loss of function impairs self-grooming and post-stress anxiety alleviation. The findings suggest a dual role of the CeA-MPLSST-VTA-DA circuit in stress and reward processing.
The use of body-focused repetitive behaviors (BFRBs) is conceptualized as a means of coping with stress. However, the neurological mechanism by which repetitive behaviors affect anxiety regulation is unclear. Here, we identify that the excitatory somatostatin-positive neurons in the medial paralemniscal nucleus (MPLSST neurons) in mice promote self-grooming and encode reward. MPLSST neurons display prominent grooming-related neuronal activity. Loss of function of MPLSST neurons impairs both self-grooming and post-stress anxiety alleviation. Activation of MPLSST neurons is rewarding and sufficient to drive reinforce-ment by activating dopamine (DA) neurons in the ventral tegmental area (VTA) and eliciting dopamine release. The neuropeptide SST facilitates the rewarding impact of MPLSST neurons. MPLSST neuron-mediated self -grooming is triggered by the input from the central amygdala (CeA). Our study reveals a dual role of CeA-MPLSST-VTADA circuit in self-grooming and post-stress anxiety regulation and conceptualizes MPLSST neu-rons as an interface linking the stress and reward systems in mice.

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