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Bile Acid Signaling Pathways from the Enterohepatic Circulation to the Central Nervous System

Bile acids are best known as detergents involved in the digestion of lipids. In addition, new data in the last decade have shown that bile acids also function as gut hormones capable of influencing metabolic processes via receptors such as FXR (farnesoid X receptor) and TGR5 (Takeda G protein-couple...

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Autores principales: Mertens, Kim L., Kalsbeek, Andries, Soeters, Maarten R., Eggink, Hannah M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5681992/
https://www.ncbi.nlm.nih.gov/pubmed/29163019
http://dx.doi.org/10.3389/fnins.2017.00617
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author Mertens, Kim L.
Kalsbeek, Andries
Soeters, Maarten R.
Eggink, Hannah M.
author_facet Mertens, Kim L.
Kalsbeek, Andries
Soeters, Maarten R.
Eggink, Hannah M.
author_sort Mertens, Kim L.
collection PubMed
description Bile acids are best known as detergents involved in the digestion of lipids. In addition, new data in the last decade have shown that bile acids also function as gut hormones capable of influencing metabolic processes via receptors such as FXR (farnesoid X receptor) and TGR5 (Takeda G protein-coupled receptor 5). These effects of bile acids are not restricted to the gastrointestinal tract, but can affect different tissues throughout the organism. It is still unclear whether these effects also involve signaling of bile acids to the central nervous system (CNS). Bile acid signaling to the CNS encompasses both direct and indirect pathways. Bile acids can act directly in the brain via central FXR and TGR5 signaling. In addition, there are two indirect pathways that involve intermediate agents released upon interaction with bile acids receptors in the gut. Activation of intestinal FXR and TGR5 receptors can result in the release of fibroblast growth factor 19 (FGF19) and glucagon-like peptide 1 (GLP-1), both capable of signaling to the CNS. We conclude that when plasma bile acids levels are high all three pathways may contribute in signal transmission to the CNS. However, under normal physiological circumstances, the indirect pathway involving GLP-1 may evoke the most substantial effect in the brain.
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spelling pubmed-56819922017-11-21 Bile Acid Signaling Pathways from the Enterohepatic Circulation to the Central Nervous System Mertens, Kim L. Kalsbeek, Andries Soeters, Maarten R. Eggink, Hannah M. Front Neurosci Neuroscience Bile acids are best known as detergents involved in the digestion of lipids. In addition, new data in the last decade have shown that bile acids also function as gut hormones capable of influencing metabolic processes via receptors such as FXR (farnesoid X receptor) and TGR5 (Takeda G protein-coupled receptor 5). These effects of bile acids are not restricted to the gastrointestinal tract, but can affect different tissues throughout the organism. It is still unclear whether these effects also involve signaling of bile acids to the central nervous system (CNS). Bile acid signaling to the CNS encompasses both direct and indirect pathways. Bile acids can act directly in the brain via central FXR and TGR5 signaling. In addition, there are two indirect pathways that involve intermediate agents released upon interaction with bile acids receptors in the gut. Activation of intestinal FXR and TGR5 receptors can result in the release of fibroblast growth factor 19 (FGF19) and glucagon-like peptide 1 (GLP-1), both capable of signaling to the CNS. We conclude that when plasma bile acids levels are high all three pathways may contribute in signal transmission to the CNS. However, under normal physiological circumstances, the indirect pathway involving GLP-1 may evoke the most substantial effect in the brain. Frontiers Media S.A. 2017-11-07 /pmc/articles/PMC5681992/ /pubmed/29163019 http://dx.doi.org/10.3389/fnins.2017.00617 Text en Copyright © 2017 Mertens, Kalsbeek, Soeters and Eggink. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Mertens, Kim L.
Kalsbeek, Andries
Soeters, Maarten R.
Eggink, Hannah M.
Bile Acid Signaling Pathways from the Enterohepatic Circulation to the Central Nervous System
title Bile Acid Signaling Pathways from the Enterohepatic Circulation to the Central Nervous System
title_full Bile Acid Signaling Pathways from the Enterohepatic Circulation to the Central Nervous System
title_fullStr Bile Acid Signaling Pathways from the Enterohepatic Circulation to the Central Nervous System
title_full_unstemmed Bile Acid Signaling Pathways from the Enterohepatic Circulation to the Central Nervous System
title_short Bile Acid Signaling Pathways from the Enterohepatic Circulation to the Central Nervous System
title_sort bile acid signaling pathways from the enterohepatic circulation to the central nervous system
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5681992/
https://www.ncbi.nlm.nih.gov/pubmed/29163019
http://dx.doi.org/10.3389/fnins.2017.00617
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