Hammack Sayamwong E, Braas Karen M, May Victor
Department of Psychological Science, University of Vermont, Burlington, VT, United States.
Department of Neurological Sciences, University of Vermont Larner College of Medicine, Burlington, VT, United States.
Handb Clin Neurol. 2021;179:385-402. doi: 10.1016/B978-0-12-819975-6.00025-X.
The bed nucleus of the stria terminalis (BNST) is a compact but neurophenotypically complex structure in the ventral forebrain that is structurally and functionally linked to other limbic structures, including the amygdala nuclear complex, hypothalamic nuclei, hippocampus, and related midbrain structures, to participate in a wide range of functions, especially emotion, emotional learning, stress-related responses, and sexual behaviors. From a variety of sensory inputs, the BNST acts as a node for signal integration and coordination for information relay to downstream central neuroendocrine and autonomic centers for appropriate homeostatic physiological and behavioral responses. In contrast to the role of the amygdala in fear, the BNST has gained wide interest from work suggesting that it has main roles in mediating sustained responses to diffuse, unpredictable and/or long-duration threats that are typically associated with anxiety-related responses. Further, some BNST subregions are highly sexually dimorphic which appear contributory to the differential stress and social interactive behaviors, including reproductive responses, between males and females. Notably, maladaptive BNST neuroplasticity and function have been implicated in chronic pain, depression, anxiety-related abnormalities, and other psychopathologies including posttraumatic stress disorders. The BNST circuits are predominantly GABAergic-the glutaminergic neurons represent a minor population-but the complexity of the system results from an overlay of diverse neuropeptide coexpression in these neurons. More than a dozen neuropeptides may be differentially coexpressed in BNST neurons, and from variable G protein-coupled receptor signaling, may inhibit or activate downstream circuit activities. The mechanisms and roles of these peptides in modulating intrinsic BNST neurocircuit signaling and BNST long-distance target cell projections are still not well understood. Nevertheless, an understanding of some of the principal players may allow assembly of the circuit interactions.
终纹床核(BNST)是腹侧前脑一个紧凑但神经表型复杂的结构,在结构和功能上与其他边缘系统结构相连,包括杏仁核复合体、下丘脑核、海马体及相关中脑结构,参与广泛的功能,尤其是情绪、情绪学习、应激相关反应和性行为。从各种感觉输入来看,BNST作为信号整合与协调的节点,将信息中继至下游中枢神经内分泌和自主神经中枢,以产生适当的稳态生理和行为反应。与杏仁核在恐惧中的作用不同,BNST因以下研究而备受关注:研究表明,它在介导对弥漫性、不可预测和/或长期威胁的持续反应中起主要作用,这些威胁通常与焦虑相关反应有关。此外,BNST的一些亚区域具有高度的性别二态性,这似乎导致了雄性和雌性在应激和社会互动行为(包括生殖反应)上的差异。值得注意的是,BNST的适应不良神经可塑性和功能与慢性疼痛、抑郁症、焦虑相关异常以及其他精神病理学(包括创伤后应激障碍)有关。BNST回路主要是γ-氨基丁酸能的——谷氨酸能神经元占少数——但该系统的复杂性源于这些神经元中多种神经肽共表达的叠加。十几种神经肽可能在BNST神经元中差异共表达,并且通过可变的G蛋白偶联受体信号传导,可能抑制或激活下游回路活动。这些肽在调节BNST内在神经回路信号传导和BNST远距离靶细胞投射中的机制和作用仍未完全了解。然而,了解一些主要参与者可能有助于构建回路相互作用。