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Metabolic Diffusion in Neuropathologies: The Relevance of Brain-Liver Axis

Chronic liver diseases include a broad group of hepatic disorders from different etiologies and with varying degrees of progression and severity. Among them, non-alcoholic fatty (NAFLD) and alcoholic (ALD) liver diseases are the most frequent forms of expression, caused by either metabolic alteratio...

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Autores principales: Vegas-Suárez, Sergio, Simón, Jorge, Martínez-Chantar, María Luz, Moratalla, Rosario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9134112/
https://www.ncbi.nlm.nih.gov/pubmed/35634148
http://dx.doi.org/10.3389/fphys.2022.864263
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author Vegas-Suárez, Sergio
Simón, Jorge
Martínez-Chantar, María Luz
Moratalla, Rosario
author_facet Vegas-Suárez, Sergio
Simón, Jorge
Martínez-Chantar, María Luz
Moratalla, Rosario
author_sort Vegas-Suárez, Sergio
collection PubMed
description Chronic liver diseases include a broad group of hepatic disorders from different etiologies and with varying degrees of progression and severity. Among them, non-alcoholic fatty (NAFLD) and alcoholic (ALD) liver diseases are the most frequent forms of expression, caused by either metabolic alterations or chronic alcohol consumption. The liver is the main regulator of energy homeostasis and metabolism of potentially toxic compounds in the organism, thus hepatic disorders often promote the release of harmful substances. In this context, there is an existing interconnection between liver and brain, with the well-named brain-liver axis, in which liver pathologies lead to the promotion of neurodegenerative disorders. Alzheimer’s (AD) and Parkinson’s (PD) diseases are the most relevant neurological disorders worldwide. The present work highlights the relevance of the liver-related promotion of these disorders. Liver-related hyperammonemia has been related to the promotion of perturbations in nervous systems, whereas the production of ketone bodies under certain conditions may protect from developing them. The capacity of the liver of amyloid-β (Aβ) clearance is reduced under liver pathologies, contributing to the development of AD. These perturbations are even aggravated by the pro-inflammatory state that often accompanies liver diseases, leading to the named neuroinflammation. The current nourishment habits, named as Western diet (WD) and alterations in the bile acid (BA) profile, whose homeostasis is controlled by the liver, have been also related to both AD and PD, whereas the supplementation with certain compounds, has been demonstrated to alleviate the pathologies.
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spelling pubmed-91341122022-05-27 Metabolic Diffusion in Neuropathologies: The Relevance of Brain-Liver Axis Vegas-Suárez, Sergio Simón, Jorge Martínez-Chantar, María Luz Moratalla, Rosario Front Physiol Physiology Chronic liver diseases include a broad group of hepatic disorders from different etiologies and with varying degrees of progression and severity. Among them, non-alcoholic fatty (NAFLD) and alcoholic (ALD) liver diseases are the most frequent forms of expression, caused by either metabolic alterations or chronic alcohol consumption. The liver is the main regulator of energy homeostasis and metabolism of potentially toxic compounds in the organism, thus hepatic disorders often promote the release of harmful substances. In this context, there is an existing interconnection between liver and brain, with the well-named brain-liver axis, in which liver pathologies lead to the promotion of neurodegenerative disorders. Alzheimer’s (AD) and Parkinson’s (PD) diseases are the most relevant neurological disorders worldwide. The present work highlights the relevance of the liver-related promotion of these disorders. Liver-related hyperammonemia has been related to the promotion of perturbations in nervous systems, whereas the production of ketone bodies under certain conditions may protect from developing them. The capacity of the liver of amyloid-β (Aβ) clearance is reduced under liver pathologies, contributing to the development of AD. These perturbations are even aggravated by the pro-inflammatory state that often accompanies liver diseases, leading to the named neuroinflammation. The current nourishment habits, named as Western diet (WD) and alterations in the bile acid (BA) profile, whose homeostasis is controlled by the liver, have been also related to both AD and PD, whereas the supplementation with certain compounds, has been demonstrated to alleviate the pathologies. Frontiers Media S.A. 2022-05-12 /pmc/articles/PMC9134112/ /pubmed/35634148 http://dx.doi.org/10.3389/fphys.2022.864263 Text en Copyright © 2022 Vegas-Suárez, Simón, Martínez-Chantar and Moratalla. https://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) and the copyright owner(s) 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 Physiology
Vegas-Suárez, Sergio
Simón, Jorge
Martínez-Chantar, María Luz
Moratalla, Rosario
Metabolic Diffusion in Neuropathologies: The Relevance of Brain-Liver Axis
title Metabolic Diffusion in Neuropathologies: The Relevance of Brain-Liver Axis
title_full Metabolic Diffusion in Neuropathologies: The Relevance of Brain-Liver Axis
title_fullStr Metabolic Diffusion in Neuropathologies: The Relevance of Brain-Liver Axis
title_full_unstemmed Metabolic Diffusion in Neuropathologies: The Relevance of Brain-Liver Axis
title_short Metabolic Diffusion in Neuropathologies: The Relevance of Brain-Liver Axis
title_sort metabolic diffusion in neuropathologies: the relevance of brain-liver axis
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9134112/
https://www.ncbi.nlm.nih.gov/pubmed/35634148
http://dx.doi.org/10.3389/fphys.2022.864263
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