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The Biosynthesis, Signaling, and Neurological Functions of Bile Acids

Bile acids (BA) are amphipathic steroid acids synthesized from cholesterol in the liver. They act as detergents to expedite the digestion and absorption of dietary lipids and lipophilic vitamins. BA are also considered to be signaling molecules, being ligands of nuclear and cell-surface receptors, i...

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Detalles Bibliográficos
Autores principales: Kiriyama, Yoshimitsu, Nochi, Hiromi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6628048/
https://www.ncbi.nlm.nih.gov/pubmed/31208099
http://dx.doi.org/10.3390/biom9060232
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author Kiriyama, Yoshimitsu
Nochi, Hiromi
author_facet Kiriyama, Yoshimitsu
Nochi, Hiromi
author_sort Kiriyama, Yoshimitsu
collection PubMed
description Bile acids (BA) are amphipathic steroid acids synthesized from cholesterol in the liver. They act as detergents to expedite the digestion and absorption of dietary lipids and lipophilic vitamins. BA are also considered to be signaling molecules, being ligands of nuclear and cell-surface receptors, including farnesoid X receptor and Takeda G-protein receptor 5. Moreover, BA also activate ion channels, including the bile acid-sensitive ion channel and epithelial Na(+) channel. BA regulate glucose and lipid metabolism by activating these receptors in peripheral tissues, such as the liver and brown and white adipose tissue. Recently, 20 different BA have been identified in the central nervous system. Furthermore, BA affect the function of neurotransmitter receptors, such as the muscarinic acetylcholine receptor and γ-aminobutyric acid receptor. BA are also known to be protective against neurodegeneration. Here, we review recent findings regarding the biosynthesis, signaling, and neurological functions of BA.
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spelling pubmed-66280482019-07-23 The Biosynthesis, Signaling, and Neurological Functions of Bile Acids Kiriyama, Yoshimitsu Nochi, Hiromi Biomolecules Review Bile acids (BA) are amphipathic steroid acids synthesized from cholesterol in the liver. They act as detergents to expedite the digestion and absorption of dietary lipids and lipophilic vitamins. BA are also considered to be signaling molecules, being ligands of nuclear and cell-surface receptors, including farnesoid X receptor and Takeda G-protein receptor 5. Moreover, BA also activate ion channels, including the bile acid-sensitive ion channel and epithelial Na(+) channel. BA regulate glucose and lipid metabolism by activating these receptors in peripheral tissues, such as the liver and brown and white adipose tissue. Recently, 20 different BA have been identified in the central nervous system. Furthermore, BA affect the function of neurotransmitter receptors, such as the muscarinic acetylcholine receptor and γ-aminobutyric acid receptor. BA are also known to be protective against neurodegeneration. Here, we review recent findings regarding the biosynthesis, signaling, and neurological functions of BA. MDPI 2019-06-15 /pmc/articles/PMC6628048/ /pubmed/31208099 http://dx.doi.org/10.3390/biom9060232 Text en © 2019 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
Kiriyama, Yoshimitsu
Nochi, Hiromi
The Biosynthesis, Signaling, and Neurological Functions of Bile Acids
title The Biosynthesis, Signaling, and Neurological Functions of Bile Acids
title_full The Biosynthesis, Signaling, and Neurological Functions of Bile Acids
title_fullStr The Biosynthesis, Signaling, and Neurological Functions of Bile Acids
title_full_unstemmed The Biosynthesis, Signaling, and Neurological Functions of Bile Acids
title_short The Biosynthesis, Signaling, and Neurological Functions of Bile Acids
title_sort biosynthesis, signaling, and neurological functions of bile acids
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6628048/
https://www.ncbi.nlm.nih.gov/pubmed/31208099
http://dx.doi.org/10.3390/biom9060232
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