Brain Research Institute, Jeffrey Cheah School of Medicine and Health Sciences, Monash University Malaysia, Bandar Sunway, Selangor, Malaysia.
Neurosci Biobehav Rev. 2022 Jan;132:870-883. doi: 10.1016/j.neubiorev.2021.11.008. Epub 2021 Nov 18.
The phasic emotion, fear, and the tonic emotion, anxiety, have been conventionally inspected in clinical frameworks to epitomize memory acquisition, storage, and retrieval. However, inappropriate expression of learned fear in a safe environment and its resistance to suppression is a cardinal feature of various fear-related disorders. A significant body of literature suggests the involvement of extra-amygdala circuitry in fear disorders. Consistent with this view, the present review underlies incentives for the association between the habenula and fear memory. G protein-coupled receptors (GPCRs) are important to understand the molecular mechanisms central to fear learning due to their neuromodulatory role. The efficacy of a pharmacological strategy aimed at exploiting habenular-GPCR desensitization machinery can serve as a therapeutic target combating the pathophysiology of fear disorders. Originating from this milieu, the conserved nature of orphan GPCRs in the brain, with some having the highest expression in the habenula can lead to recent endeavors in understanding its functionality in fear circuitry.
在临床框架中,人们通常会检查阶段性情绪(恐惧)和紧张性情绪(焦虑),以概括记忆的获取、存储和检索。然而,在安全环境中表现出不适当的习得性恐惧,以及其对抑制的抵抗力,是各种与恐惧相关障碍的一个主要特征。大量文献表明,杏仁体外的神经回路参与了恐惧障碍。与这一观点一致,本综述强调了海勒氏神经核与恐惧记忆之间的联系。由于其神经调制作用,G 蛋白偶联受体(GPCRs)对于理解恐惧学习的核心分子机制非常重要。一种旨在利用海勒氏神经核-GPCR 脱敏机制的药物策略的疗效可以作为对抗恐惧障碍病理生理学的治疗靶点。从这个环境中,大脑中孤儿 GPCR 的保守性质,其中一些在海勒氏神经核中表达最高,可以导致最近在理解其在恐惧回路中的功能方面的努力。