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FAT/CD36 Participation in Human Skeletal Muscle Lipid Metabolism: A Systematic Review
Fatty acid translocase/cluster of differentiation 36 (FAT/CD36) is a multifunctional membrane protein activated by a high-fat diet, physical exercise, fatty acids (FAs), leptin, and insulin. The principal function of FAT/CD36 is to facilitate the transport of long-chain fatty acids through cell memb...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9821548/ https://www.ncbi.nlm.nih.gov/pubmed/36615118 http://dx.doi.org/10.3390/jcm12010318 |
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author | Ramos-Jiménez, Arnulfo Zavala-Lira, Ruth A. Moreno-Brito, Verónica González-Rodríguez, Everardo |
author_facet | Ramos-Jiménez, Arnulfo Zavala-Lira, Ruth A. Moreno-Brito, Verónica González-Rodríguez, Everardo |
author_sort | Ramos-Jiménez, Arnulfo |
collection | PubMed |
description | Fatty acid translocase/cluster of differentiation 36 (FAT/CD36) is a multifunctional membrane protein activated by a high-fat diet, physical exercise, fatty acids (FAs), leptin, and insulin. The principal function of FAT/CD36 is to facilitate the transport of long-chain fatty acids through cell membranes such as myocytes, adipocytes, heart, and liver. Under high-energy expenditure, the different isoforms of FAT/CD36 in the plasma membrane and mitochondria bind to the mobilization and oxidation of FAs. Furthermore, FAT/CD36 is released in its soluble form and becomes a marker of metabolic dysfunction. Studies with healthy animals and humans show that physical exercise and a high-lipid diet increase FAT/CD36 expression and caloric expenditure. However, several aspects such as obesity, diabetes, Single Nucleotide polymorphisms (SNPs), and oxidative stress affect the normal FAs metabolism and function of FAT/CD36, inducing metabolic disease. Through a comprehensive systematic review of primary studies, this work aimed to document molecular mechanisms related to FAT/CD36 in FAs oxidation and trafficking in skeletal muscle under basal conditions, physical exercise, and diet in healthy individuals. |
format | Online Article Text |
id | pubmed-9821548 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-98215482023-01-07 FAT/CD36 Participation in Human Skeletal Muscle Lipid Metabolism: A Systematic Review Ramos-Jiménez, Arnulfo Zavala-Lira, Ruth A. Moreno-Brito, Verónica González-Rodríguez, Everardo J Clin Med Review Fatty acid translocase/cluster of differentiation 36 (FAT/CD36) is a multifunctional membrane protein activated by a high-fat diet, physical exercise, fatty acids (FAs), leptin, and insulin. The principal function of FAT/CD36 is to facilitate the transport of long-chain fatty acids through cell membranes such as myocytes, adipocytes, heart, and liver. Under high-energy expenditure, the different isoforms of FAT/CD36 in the plasma membrane and mitochondria bind to the mobilization and oxidation of FAs. Furthermore, FAT/CD36 is released in its soluble form and becomes a marker of metabolic dysfunction. Studies with healthy animals and humans show that physical exercise and a high-lipid diet increase FAT/CD36 expression and caloric expenditure. However, several aspects such as obesity, diabetes, Single Nucleotide polymorphisms (SNPs), and oxidative stress affect the normal FAs metabolism and function of FAT/CD36, inducing metabolic disease. Through a comprehensive systematic review of primary studies, this work aimed to document molecular mechanisms related to FAT/CD36 in FAs oxidation and trafficking in skeletal muscle under basal conditions, physical exercise, and diet in healthy individuals. MDPI 2022-12-31 /pmc/articles/PMC9821548/ /pubmed/36615118 http://dx.doi.org/10.3390/jcm12010318 Text en © 2022 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 Ramos-Jiménez, Arnulfo Zavala-Lira, Ruth A. Moreno-Brito, Verónica González-Rodríguez, Everardo FAT/CD36 Participation in Human Skeletal Muscle Lipid Metabolism: A Systematic Review |
title | FAT/CD36 Participation in Human Skeletal Muscle Lipid Metabolism: A Systematic Review |
title_full | FAT/CD36 Participation in Human Skeletal Muscle Lipid Metabolism: A Systematic Review |
title_fullStr | FAT/CD36 Participation in Human Skeletal Muscle Lipid Metabolism: A Systematic Review |
title_full_unstemmed | FAT/CD36 Participation in Human Skeletal Muscle Lipid Metabolism: A Systematic Review |
title_short | FAT/CD36 Participation in Human Skeletal Muscle Lipid Metabolism: A Systematic Review |
title_sort | fat/cd36 participation in human skeletal muscle lipid metabolism: a systematic review |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9821548/ https://www.ncbi.nlm.nih.gov/pubmed/36615118 http://dx.doi.org/10.3390/jcm12010318 |
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