Department of Psychological and Brain Sciences, Texas A&M University, College Station, TX 77843-4235.
Institute for Neuroscience, Texas A&M University, College Station, TX 77843-3474.
Proc Natl Acad Sci U S A. 2019 Apr 23;116(17):8570-8575. doi: 10.1073/pnas.1814278116. Epub 2019 Apr 10.
The medial prefrontal cortex (mPFC) plays an essential role in regulating emotion, including inhibiting fear when danger has passed. The extinction of fear, however, is labile and a number of factors, including stress, cause extinguished fear to relapse. Here we show that fear relapse in rats limits single-unit activity among infralimbic (IL) neurons, which are critical for inhibiting fear responses, and facilitates activity in prelimbic (PL) neurons involved in fear expression. Pharmacogenetic activation of noradrenergic neurons in the locus coeruleus mimics this shift in reciprocal IL-PL spike firing, increases the expression of conditioned freezing behavior, and causes relapse of extinguished fear. Noradrenergic modulation of mPFC firing represents a mechanism for relapse and a potential target for therapeutic interventions to reduce pathological fear.
内侧前额叶皮层(mPFC)在调节情绪方面起着至关重要的作用,包括在危险过去时抑制恐惧。然而,恐惧的消除是不稳定的,许多因素,包括压力,会导致已消除的恐惧重新出现。在这里,我们发现大鼠的恐惧复发限制了内侧眶额皮层(IL)神经元的单个单元活动,而这些神经元对于抑制恐惧反应至关重要,并且促进了参与恐惧表达的外侧眶额皮层(PL)神经元的活动。蓝斑核内去甲肾上腺素能神经元的药理学遗传激活模拟了这种反向 IL-PL 尖峰放电活动的转变,增加了条件性冻结行为的表达,并导致已消除的恐惧复发。mPFC 放电的去甲肾上腺素能调节代表了复发的一种机制,也是减少病理性恐惧的治疗干预的潜在目标。