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Rho GTPases in the Amygdala—A Switch for Fears?
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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7563696/ https://www.ncbi.nlm.nih.gov/pubmed/32858950 http://dx.doi.org/10.3390/cells9091972 |
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author | Sarowar, Tasnuva Grabrucker, Andreas M. |
author_facet | Sarowar, Tasnuva Grabrucker, Andreas M. |
author_sort | Sarowar, Tasnuva |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7563696 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-75636962020-10-27 Rho GTPases in the Amygdala—A Switch for Fears? Sarowar, Tasnuva Grabrucker, Andreas M. Cells Review 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. MDPI 2020-08-26 /pmc/articles/PMC7563696/ /pubmed/32858950 http://dx.doi.org/10.3390/cells9091972 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Sarowar, Tasnuva Grabrucker, Andreas M. Rho GTPases in the Amygdala—A Switch for Fears? |
title | Rho GTPases in the Amygdala—A Switch for Fears? |
title_full | Rho GTPases in the Amygdala—A Switch for Fears? |
title_fullStr | Rho GTPases in the Amygdala—A Switch for Fears? |
title_full_unstemmed | Rho GTPases in the Amygdala—A Switch for Fears? |
title_short | Rho GTPases in the Amygdala—A Switch for Fears? |
title_sort | rho gtpases in the amygdala—a switch for fears? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7563696/ https://www.ncbi.nlm.nih.gov/pubmed/32858950 http://dx.doi.org/10.3390/cells9091972 |
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