Interdisciplinary Neuroscience Program.
Department of Psychological and Brain Sciences.
J Neurosci. 2019 Feb 20;39(8):1405-1419. doi: 10.1523/JNEUROSCI.1421-18.2018. Epub 2018 Dec 20.
One of the challenges facing neuroscience entails localization of circuits and mechanisms accounting for how multiple features of stress responses are organized to promote survival during adverse experiences. The rodent medial prefrontal cortex (mPFC) is generally regarded as a key site for cognitive and affective information processing, and the anteroventral bed nuclei of the stria terminalis (avBST) integrates homeostatic information from a variety of sources, including the mPFC. Thus, we proposed that the mPFC is capable of generating multiple features (endocrine, behavioral) of adaptive responses via its influence over the avBST. To address this possibility, we first optogenetically inhibited input to avBST from the rostral prelimbic cortical region of mPFC and observed concurrent increases in immobility and hypothalamo-pituitary-adrenal (HPA) output in male rats during tail suspension, whereas photostimulation of this pathway decreased immobility during the same challenge. Anatomical tracing experiments confirmed projections from the rostral prelimbic subfield to separate populations of avBST neurons, and from these to HPA effector neurons in the paraventricular hypothalamic nucleus, and to aspects of the midbrain periaqueductal gray that coordinate passive defensive behaviors. Finally, stimulation and inhibition of the prelimbic-avBST pathway, respectively, decreased and increased passive coping in the shock-probe defensive burying test, without having any direct effect on active coping (burying) behavior. These results define a new neural substrate in the coordination of a that involves the gating of passive, rather than active, coping behaviors while restraining neuroendocrine activation to optimize adaptation during threat exposure. The circuits and mechanisms accounting for how multiple features of responses are organized to promote adaptation have yet to be elucidated. Our report identifies a prefrontal-bed nucleus pathway that organizes a capable of gating passive coping behaviors while concurrently restraining neuroendocrine activation during exposure to inescapable stressors. These data provide insight into the central organization of how multiple features of responses are integrated to promote adaptation during adverse experiences, and how disruption in one neural pathway may underlie a broad array of maladaptive responses in stress-related psychiatric disorders.
神经科学面临的挑战之一是定位负责组织多种应激反应特征以促进在不利经历中生存的回路和机制。啮齿动物的前额皮质(mPFC)通常被认为是认知和情感信息处理的关键部位,而终纹床核的前腹侧核(avBST)整合来自多种来源的内稳态信息,包括 mPFC。因此,我们提出 mPFC 能够通过其对 avBST 的影响产生多种适应性反应的特征(内分泌、行为)。为了研究这种可能性,我们首先用光遗传抑制了 mPFC 的额前皮质区对 avBST 的输入,并观察到雄性大鼠在悬尾时同时出现不动性和下丘脑-垂体-肾上腺(HPA)输出增加,而该通路的光刺激减少了在相同挑战期间的不动性。解剖示踪实验证实了来自额前皮质亚区的投射到 avBST 神经元的不同群体,以及来自这些神经元到下丘脑室旁核的 HPA 效应神经元的投射,以及协调被动防御行为的中脑导水管周围灰质的各个方面。最后,分别刺激和抑制额前皮质-avBST 通路分别减少和增加了在电击探头防御性埋藏测试中的被动应对行为,而对主动应对(埋藏)行为没有任何直接影响。这些结果定义了一个新的神经基质,涉及协调一种,该涉及被动应对行为的门控,而不是主动应对行为,同时抑制神经内分泌激活以优化在威胁暴露期间的适应。负责组织多种反应特征以促进适应的回路和机制仍有待阐明。我们的报告确定了一个前额叶-核团通路,该通路组织了一种能够在暴露于不可避免的应激源时门控被动应对行为,同时抑制神经内分泌激活的能力。这些数据提供了对整合多种反应特征以促进在不利经历中适应的中枢组织的深入了解,以及一种神经通路的中断如何可能是与应激相关的精神障碍中广泛的适应不良反应的基础。