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Signaling pathways in obesity: mechanisms and therapeutic interventions
Obesity is a complex, chronic disease and global public health challenge. Characterized by excessive fat accumulation in the body, obesity sharply increases the risk of several diseases, such as type 2 diabetes, cardiovascular disease, and nonalcoholic fatty liver disease, and is linked to lower lif...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9420733/ https://www.ncbi.nlm.nih.gov/pubmed/36031641 http://dx.doi.org/10.1038/s41392-022-01149-x |
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author | Wen, Xue Zhang, Bohan Wu, Beiyi Xiao, Haitao Li, Zehua Li, Ruoyu Xu, Xuewen Li, Tao |
author_facet | Wen, Xue Zhang, Bohan Wu, Beiyi Xiao, Haitao Li, Zehua Li, Ruoyu Xu, Xuewen Li, Tao |
author_sort | Wen, Xue |
collection | PubMed |
description | Obesity is a complex, chronic disease and global public health challenge. Characterized by excessive fat accumulation in the body, obesity sharply increases the risk of several diseases, such as type 2 diabetes, cardiovascular disease, and nonalcoholic fatty liver disease, and is linked to lower life expectancy. Although lifestyle intervention (diet and exercise) has remarkable effects on weight management, achieving long-term success at weight loss is extremely challenging, and the prevalence of obesity continues to rise worldwide. Over the past decades, the pathophysiology of obesity has been extensively investigated, and an increasing number of signal transduction pathways have been implicated in obesity, making it possible to fight obesity in a more effective and precise way. In this review, we summarize recent advances in the pathogenesis of obesity from both experimental and clinical studies, focusing on signaling pathways and their roles in the regulation of food intake, glucose homeostasis, adipogenesis, thermogenesis, and chronic inflammation. We also discuss the current anti-obesity drugs, as well as weight loss compounds in clinical trials, that target these signals. The evolving knowledge of signaling transduction may shed light on the future direction of obesity research, as we move into a new era of precision medicine. |
format | Online Article Text |
id | pubmed-9420733 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-94207332022-08-30 Signaling pathways in obesity: mechanisms and therapeutic interventions Wen, Xue Zhang, Bohan Wu, Beiyi Xiao, Haitao Li, Zehua Li, Ruoyu Xu, Xuewen Li, Tao Signal Transduct Target Ther Review Article Obesity is a complex, chronic disease and global public health challenge. Characterized by excessive fat accumulation in the body, obesity sharply increases the risk of several diseases, such as type 2 diabetes, cardiovascular disease, and nonalcoholic fatty liver disease, and is linked to lower life expectancy. Although lifestyle intervention (diet and exercise) has remarkable effects on weight management, achieving long-term success at weight loss is extremely challenging, and the prevalence of obesity continues to rise worldwide. Over the past decades, the pathophysiology of obesity has been extensively investigated, and an increasing number of signal transduction pathways have been implicated in obesity, making it possible to fight obesity in a more effective and precise way. In this review, we summarize recent advances in the pathogenesis of obesity from both experimental and clinical studies, focusing on signaling pathways and their roles in the regulation of food intake, glucose homeostasis, adipogenesis, thermogenesis, and chronic inflammation. We also discuss the current anti-obesity drugs, as well as weight loss compounds in clinical trials, that target these signals. The evolving knowledge of signaling transduction may shed light on the future direction of obesity research, as we move into a new era of precision medicine. Nature Publishing Group UK 2022-08-28 /pmc/articles/PMC9420733/ /pubmed/36031641 http://dx.doi.org/10.1038/s41392-022-01149-x Text en © The Author(s) 2022, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Article Wen, Xue Zhang, Bohan Wu, Beiyi Xiao, Haitao Li, Zehua Li, Ruoyu Xu, Xuewen Li, Tao Signaling pathways in obesity: mechanisms and therapeutic interventions |
title | Signaling pathways in obesity: mechanisms and therapeutic interventions |
title_full | Signaling pathways in obesity: mechanisms and therapeutic interventions |
title_fullStr | Signaling pathways in obesity: mechanisms and therapeutic interventions |
title_full_unstemmed | Signaling pathways in obesity: mechanisms and therapeutic interventions |
title_short | Signaling pathways in obesity: mechanisms and therapeutic interventions |
title_sort | signaling pathways in obesity: mechanisms and therapeutic interventions |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9420733/ https://www.ncbi.nlm.nih.gov/pubmed/36031641 http://dx.doi.org/10.1038/s41392-022-01149-x |
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