Cell and Molecular Biology Department, Tulane University, New Orleans, LA 70118, USA.
Neuroscience Program, Tulane University, New Orleans, LA 70118, USA; Tulane Brain Institute, Tulane University, New Orleans, LA 70118, USA.
Cell Rep. 2022 Oct 18;41(3):111509. doi: 10.1016/j.celrep.2022.111509.
Noradrenergic afferents to hypothalamic corticotropin releasing hormone (CRH) neurons provide a major excitatory drive to the hypothalamic-pituitary-adrenal (HPA) axis via α1 adrenoreceptor activation. Noradrenergic afferents are recruited preferentially by somatic, rather than psychological, stress stimuli. Stress-induced glucocorticoids feed back onto the hypothalamus to negatively regulate the HPA axis, providing a critical autoregulatory constraint that prevents glucocorticoid overexposure and neuropathology. Whether negative feedback mechanisms target stress modality-specific HPA activation is not known. Here, we describe a desensitization of the α1 adrenoreceptor activation of the HPA axis following acute stress in male mice that is mediated by rapid glucocorticoid regulation of adrenoreceptor trafficking in CRH neurons. Glucocorticoid-induced α1 receptor trafficking desensitizes the HPA axis to a somatic but not a psychological stressor. Our findings demonstrate a rapid glucocorticoid suppression of adrenergic signaling in CRH neurons that is specific to somatic stress activation, and they reveal a rapid, stress modality-selective glucocorticoid negative feedback mechanism.
去甲肾上腺素能传入纤维到下丘脑促肾上腺皮质激素释放激素 (CRH) 神经元通过 α1 肾上腺素能受体激活为下丘脑-垂体-肾上腺 (HPA) 轴提供主要的兴奋驱动。去甲肾上腺素能传入纤维优先被躯体应激刺激而不是心理应激刺激募集。应激诱导的糖皮质激素反馈到下丘脑负调节 HPA 轴,提供了防止糖皮质激素过度暴露和神经病理学的关键自身调节限制。负反馈机制是否针对应激方式特异性 HPA 激活尚不清楚。在这里,我们描述了雄性小鼠急性应激后 HPA 轴的 α1 肾上腺素能受体激活的脱敏,这是由 CRH 神经元中糖皮质激素快速调节肾上腺素能受体贩运介导的。糖皮质激素诱导的 α1 受体贩运使 HPA 轴对躯体应激而不是心理应激原脱敏。我们的发现表明,糖皮质激素对 CRH 神经元中肾上腺素能信号的快速抑制是针对躯体应激激活的,并且它们揭示了一种快速、应激方式选择性的糖皮质激素负反馈机制。