University of Amsterdam, Amsterdam, the Netherlands; Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA, USA.
Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA, USA; School of Psychology, Korea University, Seoul, Republic of Korea.
Curr Biol. 2021 Oct 11;31(19):4388-4396.e5. doi: 10.1016/j.cub.2021.07.047. Epub 2021 Aug 12.
Discrimination between predictive and non-predictive threat stimuli decreases as threat intensity increases. The central mechanisms that mediate the transition from discriminatory to generalized threat responding remain poorly resolved. Here, we identify the stress- and dysphoria-associated kappa opioid receptor (KOR) and its ligand dynorphin (Dyn), acting in the ventral tegmental area (VTA), as a key substrate for regulating threat generalization. We identify several dynorphinergic inputs to the VTA and demonstrate that projections from the bed nucleus of the stria terminalis (BNST) and dorsal raphe nucleus (DRN) both contribute to anxiety-like behavior but differentially affect threat generalization. These data demonstrate that conditioned threat discrimination has an inverted "U" relationship with threat intensity and establish a role for KOR/Dyn signaling in the midbrain for promoting threat generalization.
随着威胁强度的增加,预测性和非预测性威胁刺激之间的区分能力下降。介导从有区别的威胁反应到普遍的威胁反应的过渡的核心机制仍未得到很好的解决。在这里,我们确定应激和抑郁相关的κ阿片受体 (KOR) 及其配体强啡肽 (Dyn),在腹侧被盖区 (VTA) 中作为调节威胁泛化的关键基质。我们确定了 VTA 的几种强啡肽能传入,并证明来自终纹床核 (BNST) 和中缝背核 (DRN) 的投射都有助于焦虑样行为,但对威胁泛化的影响不同。这些数据表明,条件性威胁辨别与威胁强度呈倒“U”关系,并确立了中脑 KOR/Dyn 信号在促进威胁泛化中的作用。