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Perspective of Small-Molecule AdipoR Agonist for Type 2 Diabetes and Short Life in Obesity
Obesity associated with unhealthy diet and lack of exercise is shown to contribute to the onset and/or aggravation of the metabolic syndrome and diabetes, thus placing affected individuals at increased risk of cardiovascular disease and cancer. Plasma adiponectin levels are decreased in obesity, whi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Diabetes Association
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4641965/ https://www.ncbi.nlm.nih.gov/pubmed/26566493 http://dx.doi.org/10.4093/dmj.2015.39.5.363 |
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author | Okada-Iwabu, Miki Iwabu, Masato Ueki, Kohjiro Yamauchi, Toshimasa Kadowaki, Takashi |
author_facet | Okada-Iwabu, Miki Iwabu, Masato Ueki, Kohjiro Yamauchi, Toshimasa Kadowaki, Takashi |
author_sort | Okada-Iwabu, Miki |
collection | PubMed |
description | Obesity associated with unhealthy diet and lack of exercise is shown to contribute to the onset and/or aggravation of the metabolic syndrome and diabetes, thus placing affected individuals at increased risk of cardiovascular disease and cancer. Plasma adiponectin levels are decreased in obesity, which causes insulin resistance and diabetes. Therefore, we identified adiponectin receptors (AdipoRs) as the therapeutic target. It was suggested that, similarly to caloric restriction and exercise, activation of the AdipoRs may have the potential not only to improve lifestyle-related diseases but to contribute to prolonged the shortened lifespan on a high caloric unhealthy diet. To this end, we have identified "AdipoRon" as an adiponectin receptor agonist. Indeed, AdipoRon ameliorated diabetes associated with obesity as well as to increase exercise endurance, thus prolonging shortened lifespan of obese mice fed on a high fat diet. Additionally, we have recently determined the crystal structures of the human AdipoRs. The seven-transmembrane helices of AdipoRs are structurally distinct from those of G-protein coupled receptors. It is expected that these findings will contribute not only to the elucidation of the AdipoR-related signal transduction but to the development and optimization of AdipoR-targeted therapeutics for obesity-related diseases such as diabetes. |
format | Online Article Text |
id | pubmed-4641965 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Korean Diabetes Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-46419652015-11-12 Perspective of Small-Molecule AdipoR Agonist for Type 2 Diabetes and Short Life in Obesity Okada-Iwabu, Miki Iwabu, Masato Ueki, Kohjiro Yamauchi, Toshimasa Kadowaki, Takashi Diabetes Metab J Review Obesity associated with unhealthy diet and lack of exercise is shown to contribute to the onset and/or aggravation of the metabolic syndrome and diabetes, thus placing affected individuals at increased risk of cardiovascular disease and cancer. Plasma adiponectin levels are decreased in obesity, which causes insulin resistance and diabetes. Therefore, we identified adiponectin receptors (AdipoRs) as the therapeutic target. It was suggested that, similarly to caloric restriction and exercise, activation of the AdipoRs may have the potential not only to improve lifestyle-related diseases but to contribute to prolonged the shortened lifespan on a high caloric unhealthy diet. To this end, we have identified "AdipoRon" as an adiponectin receptor agonist. Indeed, AdipoRon ameliorated diabetes associated with obesity as well as to increase exercise endurance, thus prolonging shortened lifespan of obese mice fed on a high fat diet. Additionally, we have recently determined the crystal structures of the human AdipoRs. The seven-transmembrane helices of AdipoRs are structurally distinct from those of G-protein coupled receptors. It is expected that these findings will contribute not only to the elucidation of the AdipoR-related signal transduction but to the development and optimization of AdipoR-targeted therapeutics for obesity-related diseases such as diabetes. Korean Diabetes Association 2015-10 2015-10-22 /pmc/articles/PMC4641965/ /pubmed/26566493 http://dx.doi.org/10.4093/dmj.2015.39.5.363 Text en Copyright © 2015 Korean Diabetes Association http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Okada-Iwabu, Miki Iwabu, Masato Ueki, Kohjiro Yamauchi, Toshimasa Kadowaki, Takashi Perspective of Small-Molecule AdipoR Agonist for Type 2 Diabetes and Short Life in Obesity |
title | Perspective of Small-Molecule AdipoR Agonist for Type 2 Diabetes and Short Life in Obesity |
title_full | Perspective of Small-Molecule AdipoR Agonist for Type 2 Diabetes and Short Life in Obesity |
title_fullStr | Perspective of Small-Molecule AdipoR Agonist for Type 2 Diabetes and Short Life in Obesity |
title_full_unstemmed | Perspective of Small-Molecule AdipoR Agonist for Type 2 Diabetes and Short Life in Obesity |
title_short | Perspective of Small-Molecule AdipoR Agonist for Type 2 Diabetes and Short Life in Obesity |
title_sort | perspective of small-molecule adipor agonist for type 2 diabetes and short life in obesity |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4641965/ https://www.ncbi.nlm.nih.gov/pubmed/26566493 http://dx.doi.org/10.4093/dmj.2015.39.5.363 |
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