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Gamma-Aminobutyric Acid Signaling in Damage Response, Metabolism, and Disease

Gamma-aminobutyric acid (GABA) plays a crucial role in signal transduction and can function as a neurotransmitter. Although many studies have been conducted on GABA in brain biology, the cellular function and physiological relevance of GABA in other metabolic organs remain unclear. Here, we will dis...

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Detalles Bibliográficos
Autores principales: Kim, Kimyeong, Yoon, Haejin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10003236/
https://www.ncbi.nlm.nih.gov/pubmed/36902014
http://dx.doi.org/10.3390/ijms24054584
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author Kim, Kimyeong
Yoon, Haejin
author_facet Kim, Kimyeong
Yoon, Haejin
author_sort Kim, Kimyeong
collection PubMed
description Gamma-aminobutyric acid (GABA) plays a crucial role in signal transduction and can function as a neurotransmitter. Although many studies have been conducted on GABA in brain biology, the cellular function and physiological relevance of GABA in other metabolic organs remain unclear. Here, we will discuss recent advances in understanding GABA metabolism with a focus on its biosynthesis and cellular functions in other organs. The mechanisms of GABA in liver biology and disease have revealed new ways to link the biosynthesis of GABA to its cellular function. By reviewing what is known about the distinct effects of GABA and GABA-mediated metabolites in physiological pathways, we provide a framework for understanding newly identified targets regulating the damage response, with implications for ameliorating metabolic diseases. With this review, we suggest that further research is necessary to develop GABA’s beneficial and toxic effects on metabolic disease progression.
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spelling pubmed-100032362023-03-11 Gamma-Aminobutyric Acid Signaling in Damage Response, Metabolism, and Disease Kim, Kimyeong Yoon, Haejin Int J Mol Sci Review Gamma-aminobutyric acid (GABA) plays a crucial role in signal transduction and can function as a neurotransmitter. Although many studies have been conducted on GABA in brain biology, the cellular function and physiological relevance of GABA in other metabolic organs remain unclear. Here, we will discuss recent advances in understanding GABA metabolism with a focus on its biosynthesis and cellular functions in other organs. The mechanisms of GABA in liver biology and disease have revealed new ways to link the biosynthesis of GABA to its cellular function. By reviewing what is known about the distinct effects of GABA and GABA-mediated metabolites in physiological pathways, we provide a framework for understanding newly identified targets regulating the damage response, with implications for ameliorating metabolic diseases. With this review, we suggest that further research is necessary to develop GABA’s beneficial and toxic effects on metabolic disease progression. MDPI 2023-02-26 /pmc/articles/PMC10003236/ /pubmed/36902014 http://dx.doi.org/10.3390/ijms24054584 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Kim, Kimyeong
Yoon, Haejin
Gamma-Aminobutyric Acid Signaling in Damage Response, Metabolism, and Disease
title Gamma-Aminobutyric Acid Signaling in Damage Response, Metabolism, and Disease
title_full Gamma-Aminobutyric Acid Signaling in Damage Response, Metabolism, and Disease
title_fullStr Gamma-Aminobutyric Acid Signaling in Damage Response, Metabolism, and Disease
title_full_unstemmed Gamma-Aminobutyric Acid Signaling in Damage Response, Metabolism, and Disease
title_short Gamma-Aminobutyric Acid Signaling in Damage Response, Metabolism, and Disease
title_sort gamma-aminobutyric acid signaling in damage response, metabolism, and disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10003236/
https://www.ncbi.nlm.nih.gov/pubmed/36902014
http://dx.doi.org/10.3390/ijms24054584
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