Sanford Christina A, Soden Marta E, Baird Madison A, Miller Samara M, Schulkin Jay, Palmiter Richard D, Clark Michael, Zweifel Larry S
Department of Pharmacology, University of Washington, Seattle, WA 98105, USA.
Department of Physiology and Biophysics, Georgetown University, Washington, DC 20057, USA; Department of Neuroscience, Georgetown University, Washington, DC 20057, USA; Department of Obstetrics and Gynecology, University of Washington, Seattle, WA 98105, USA.
Neuron. 2017 Jan 4;93(1):164-178. doi: 10.1016/j.neuron.2016.11.034. Epub 2016 Dec 22.
Fear is a graded central motive state ranging from mild to intense. As threat intensity increases, fear transitions from discriminative to generalized. The circuit mechanisms that process threats of different intensity are not well resolved. Here, we isolate a unique population of locally projecting neurons in the central nucleus of the amygdala (CeA) that produce the neuropeptide corticotropin-releasing factor (CRF). CRF-producing neurons and CRF in the CeA are required for discriminative fear, but both are dispensable for generalized fear at high US intensities. Consistent with a role in discriminative fear, CRF neurons undergo plasticity following threat conditioning and selectively respond to threat-predictive cues. We further show that excitability of genetically isolated CRF-receptive (CRFR1) neurons in the CeA is potently enhanced by CRF and that CRFR1 signaling in the CeA is critical for discriminative fear. These findings demonstrate a novel CRF gain-control circuit and show separable pathways for graded fear processing.
恐惧是一种从轻微到强烈的分级中枢动机状态。随着威胁强度的增加,恐惧从辨别性向泛化性转变。处理不同强度威胁的神经回路机制尚未完全明确。在此,我们分离出杏仁核中央核(CeA)中一群独特的局部投射神经元,它们产生神经肽促肾上腺皮质激素释放因子(CRF)。CeA中产生CRF的神经元和CRF对于辨别性恐惧是必需的,但在高非条件刺激强度下,两者对于泛化性恐惧都是可有可无的。与在辨别性恐惧中的作用一致,CRF神经元在威胁条件作用后会发生可塑性变化,并选择性地对威胁预测线索做出反应。我们进一步表明,CeA中基因分离的CRF受体(CRFR1)神经元的兴奋性被CRF强烈增强,并且CeA中的CRFR1信号传导对于辨别性恐惧至关重要。这些发现证明了一种新的CRF增益控制回路,并展示了分级恐惧处理的可分离途径。