终纹
中缝背核
扁桃形结构
神经科学
血清素
焦虑
抗焦虑药
心理学
厌恶性刺激
5-羟色胺受体
隔核
中缝核
神经递质
抑制性突触后电位
医学
受体
内科学
5-羟色胺能
中枢神经系统
精神科
作者
Catherine A. Marcinkiewcz,Christopher M. Mazzone,Giuseppe D’Agostino,Lindsay R. Halladay,J. Andrew Hardaway,Jeffrey F. DiBerto,Montserrat Navarro,Nathan W. Burnham,Claudia Cristiano,Cayce Dorrier,Gregory J. Tipton,Charu Ramakrishnan,Tamás Kozicz,Karl Deisseroth,Todd E. Thiele,Zoé A. McElligott,Andrew Holmes,Lora K. Heisler,Thomas L. Kash
出处
期刊:Nature
[Nature Portfolio]
日期:2016-08-23
卷期号:537 (7618): 97-101
被引量:436
摘要
Serotonin (also known as 5-hydroxytryptamine (5-HT)) is a neurotransmitter that has an essential role in the regulation of emotion. However, the precise circuits have not yet been defined through which aversive states are orchestrated by 5-HT. Here we show that 5-HT from the dorsal raphe nucleus (5-HTDRN) enhances fear and anxiety and activates a subpopulation of corticotropin-releasing factor (CRF) neurons in the bed nucleus of the stria terminalis (CRFBNST) in mice. Specifically, 5-HTDRN projections to the BNST, via actions at 5-HT2C receptors (5-HT2CRs), engage a CRFBNST inhibitory microcircuit that silences anxiolytic BNST outputs to the ventral tegmental area and lateral hypothalamus. Furthermore, we demonstrate that this CRFBNST inhibitory circuit underlies aversive behaviour following acute exposure to selective serotonin reuptake inhibitors (SSRIs). This early aversive effect is mediated via the corticotrophin-releasing factor type 1 receptor (CRF1R, also known as CRHR1), given that CRF1R antagonism is sufficient to prevent acute SSRI-induced enhancements in aversive learning. These results reveal an essential 5-HTDRN→CRFBNST circuit governing fear and anxiety, and provide a potential mechanistic explanation for the clinical observation of early adverse events to SSRI treatment in some patients with anxiety disorders.
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