Cellular Neurobiology and Neuro-Nanotechnology Lab, Department of Biological Sciences, University of Limerick, V94PH61 Limerick, Ireland.
Bernal Institute, University of Limerick, V94PH61 Limerick, Ireland.
Cells. 2020 Aug 26;9(9):1972. doi: 10.3390/cells9091972.
Fear is a fundamental evolutionary process for survival. However, excess or irrational fear hampers normal activity and leads to phobia. The amygdala is the primary brain region associated with fear learning and conditioning. There, Rho GTPases are molecular switches that act as signaling molecules for further downstream processes that modulate, among others, dendritic spine morphogenesis and thereby play a role in fear conditioning. The three main Rho GTPases-RhoA, Rac1, and Cdc42, together with their modulators, are known to be involved in many psychiatric disorders that affect the amygdala's fear conditioning mechanism. Rich2, a RhoGAP mainly for Rac1 and Cdc42, has been studied extensively in such regard. Here, we will discuss these effectors, along with Rich2, as a molecular switch for fears, especially in the amygdala. Understanding the role of Rho GTPases in fear controlling could be beneficial for the development of therapeutic strategies targeting conditions with abnormal fear/anxiety-like behaviors.
恐惧是一种基本的生存进化过程。然而,过度或不合理的恐惧会妨碍正常活动,并导致恐惧症。杏仁核是与恐惧学习和条件反射相关的主要大脑区域。在那里,Rho GTPases 是分子开关,作为信号分子进一步作用于调节树突棘形态发生等下游过程,从而在恐惧条件反射中发挥作用。三种主要的 Rho GTPases-RhoA、Rac1 和 Cdc42,以及它们的调节剂,已知与影响杏仁核恐惧条件反射机制的许多精神疾病有关。RhoGAP 主要针对 Rac1 和 Cdc42 的 Rich2 在这方面已经得到了广泛的研究。在这里,我们将讨论这些效应物以及 Rich2 作为恐惧的分子开关,特别是在杏仁核中。了解 Rho GTPases 在控制恐惧中的作用可能有助于开发针对异常恐惧/焦虑样行为的治疗策略。