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Neuropeptide Regulation of Fear and Anxiety: Implications of Cholecystokinin Endogenous Opioids and Neuropeptide Y

机译:神经肽调节恐惧和焦虑:胆囊蛋白内源性阿片类药物和神经肽的影响

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摘要

The neural circuitry of fear likely underlies anxiety and fear-related disorders such as specific and social phobia, panic disorder, and posttraumatic stress disorder. The primary pharmacological treatments currently utilized for these disorders include benzodiazepines, which act on the GABAergic receptor system, and antidepressants, which modulate the monamine systems. However, recent work on the regulation of fear neural circuitry suggests that specific neuropeptide modulation of this system is of critical importance. Recent reviews have examined the roles of the hypothalamic-pituitary-adrenal axis neuropeptides as well as the roles of neurotrophic factors in regulating fear. The present review, instead, will focus on three neuropeptide systems which have received less attention in recent years but which are clearly involved in regulating fear and its extinction. The endogenous opioid system, particularly activating the μ opioid receptors, has been demonstrated to regulate fear expression and extinction, possibly through functioning as an error signal within the amygdala to mark unreinforced conditioned stimuli. The cholecystokinin (CCK) system initially led to much excitement through its potential role in panic disorder. More recent work in the CCK neuropeptide pathway suggests that it may act in concordance with the endogenous cannabinoid system in the modulation of fear inhibition and extinction. Finally, older as well as very recent data suggests that neuropeptide Y (NPY) may play a very interesting role in counteracting stress effects, enhancing extinction, and enhancing resilience in fear and stress preclinical models. Future work in understanding the mechanisms of neuropeptide functioning, particularly within well-known behavioral circuits, are likely to provide fascinating new clues into the understanding of fear behavior as well as suggesting novel therapeutics for treating disorders of anxiety and fear dysregulation.
机译:恐惧的神经电路很可能是焦虑和恐惧相关的疾病,如具体和社交恐惧症,恐慌症和错误的应激障碍。目前用于这些疾病的主要药理治疗包括苯二氮卓类药物,其作用于加布肝菌受体体系和调节单胺系统的抗抑郁药。然而,最近关于恐惧神经电路的调节的工作表明,该系统的特异性神经肽调节具有至关重要的重要性。近期评论已检测下丘脑 - 垂体肾上腺轴神经肽的作用,以及神经营养因素在调节恐惧中的作用。相反,本综述将专注于近年来受到较少关注的三种神经肽系统,但这明显参与了调节恐惧及其灭绝。已经证明了内源性阿片类体系,特别是激活μ阿片受体,以调节恐惧表达和消失,可能通过作为杏仁杆菌内的误差信号来标记未原始的条件刺激。胆囊蛋白(CCK)系统最初通过其在恐慌障碍中的潜在作用产生了很大的兴奋。最近CCK神经肽途径的工作表明,它可以在恐惧抑制和消灭的调节中与内源性大麻制素系统一致作用。最后,较旧的和最近的数据表明,神经肽Y(NPY)可能在抵消应力效应,增强灭绝和增强恐惧和应力临床前模型中的复原力方面发挥非常有趣的作用。未来的工作在理解神经肽功能的机制,特别是在众所周知的行为电路中,很可能会为对恐惧行为的理解提供迷人的新线索,以及提示治疗焦虑症和恐惧失调的疾病的新疗法。

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