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Role of advanced glycation end products in mobility and considerations in possible dietary and nutritional intervention strategies
Advanced glycation end products (AGEs), a group of compounds that are formed by non-enzymatic reactions between carbonyl groups of reducing sugars and free amino groups of proteins, lipids or nucleic acids, can be obtained exogenously from diet or formed endogenously within the body. AGEs accumulate...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6180645/ https://www.ncbi.nlm.nih.gov/pubmed/30337945 http://dx.doi.org/10.1186/s12986-018-0306-7 |
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author | Chen, Jie-Hua Lin, Xu Bu, Cuihong Zhang, Xuguang |
author_facet | Chen, Jie-Hua Lin, Xu Bu, Cuihong Zhang, Xuguang |
author_sort | Chen, Jie-Hua |
collection | PubMed |
description | Advanced glycation end products (AGEs), a group of compounds that are formed by non-enzymatic reactions between carbonyl groups of reducing sugars and free amino groups of proteins, lipids or nucleic acids, can be obtained exogenously from diet or formed endogenously within the body. AGEs accumulate intracellularly and extracellularly in all tissues and body fluids and can cross-link with other proteins and thus affect their normal functions. Furthermore, AGEs can interact with specific cell surface receptors and hence alter cell intracellular signaling, gene expression, the production of reactive oxygen species and the activation of several inflammatory pathways. High levels of AGEs in diet as well as in tissues and the circulation are pathogenic to a wide range of diseases. With respect to mobility, AGEs accumulate in bones, joints and skeletal muscles, playing important roles in the development of osteoporosis, osteoarthritis, and sarcopenia with aging. This report covered the related pathological mechanisms and the potential pharmaceutical and dietary intervention strategies in reducing systemic AGEs. More prospective studies are needed to determine whether elevated serum AGEs and/or skin autofluorescence predict a decline in measures of mobility. In addition, human intervention studies are required to investigate the beneficial effects of exogenous AGEs inhibitors on mobility outcomes. |
format | Online Article Text |
id | pubmed-6180645 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61806452018-10-18 Role of advanced glycation end products in mobility and considerations in possible dietary and nutritional intervention strategies Chen, Jie-Hua Lin, Xu Bu, Cuihong Zhang, Xuguang Nutr Metab (Lond) Review Advanced glycation end products (AGEs), a group of compounds that are formed by non-enzymatic reactions between carbonyl groups of reducing sugars and free amino groups of proteins, lipids or nucleic acids, can be obtained exogenously from diet or formed endogenously within the body. AGEs accumulate intracellularly and extracellularly in all tissues and body fluids and can cross-link with other proteins and thus affect their normal functions. Furthermore, AGEs can interact with specific cell surface receptors and hence alter cell intracellular signaling, gene expression, the production of reactive oxygen species and the activation of several inflammatory pathways. High levels of AGEs in diet as well as in tissues and the circulation are pathogenic to a wide range of diseases. With respect to mobility, AGEs accumulate in bones, joints and skeletal muscles, playing important roles in the development of osteoporosis, osteoarthritis, and sarcopenia with aging. This report covered the related pathological mechanisms and the potential pharmaceutical and dietary intervention strategies in reducing systemic AGEs. More prospective studies are needed to determine whether elevated serum AGEs and/or skin autofluorescence predict a decline in measures of mobility. In addition, human intervention studies are required to investigate the beneficial effects of exogenous AGEs inhibitors on mobility outcomes. BioMed Central 2018-10-10 /pmc/articles/PMC6180645/ /pubmed/30337945 http://dx.doi.org/10.1186/s12986-018-0306-7 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Chen, Jie-Hua Lin, Xu Bu, Cuihong Zhang, Xuguang Role of advanced glycation end products in mobility and considerations in possible dietary and nutritional intervention strategies |
title | Role of advanced glycation end products in mobility and considerations in possible dietary and nutritional intervention strategies |
title_full | Role of advanced glycation end products in mobility and considerations in possible dietary and nutritional intervention strategies |
title_fullStr | Role of advanced glycation end products in mobility and considerations in possible dietary and nutritional intervention strategies |
title_full_unstemmed | Role of advanced glycation end products in mobility and considerations in possible dietary and nutritional intervention strategies |
title_short | Role of advanced glycation end products in mobility and considerations in possible dietary and nutritional intervention strategies |
title_sort | role of advanced glycation end products in mobility and considerations in possible dietary and nutritional intervention strategies |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6180645/ https://www.ncbi.nlm.nih.gov/pubmed/30337945 http://dx.doi.org/10.1186/s12986-018-0306-7 |
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