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Anti-Obesity Effect of Chitoglucan in High-Fat-Induced Obesity Mice
Background: Chitoglucan (CG) is a bioactive component obtained from Flammulina velutipes Sing, an edible mushroom, which is known to have an anti-obesity effect. However, its biological and hormonal activities in alleviating obesity through regulation of adipocyte-derived proteins have not been exam...
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/PMC9819012/ https://www.ncbi.nlm.nih.gov/pubmed/36612600 http://dx.doi.org/10.3390/ijerph20010281 |
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author | Park, Hyun-Jung Lee, SunYoung Ye, Minsook Han, Bong Hee Shim, Hyun Soo Jang, Daehyuk Shim, Insop |
author_facet | Park, Hyun-Jung Lee, SunYoung Ye, Minsook Han, Bong Hee Shim, Hyun Soo Jang, Daehyuk Shim, Insop |
author_sort | Park, Hyun-Jung |
collection | PubMed |
description | Background: Chitoglucan (CG) is a bioactive component obtained from Flammulina velutipes Sing, an edible mushroom, which is known to have an anti-obesity effect. However, its biological and hormonal activities in alleviating obesity through regulation of adipocyte-derived proteins have not been examined yet. Purpose: The present study aimed to investigate the anti-obesity effects of chitoglucan and its hormonal mechanisms in high-fat diet (HFD)-induced mice. Methods: The mice were fed either a normal diet (Normal group) or a high fat diet (HFD group) over 6 weeks. The HFD fed mice were administered with saline (HFD group), adipex (HFD + adipex group), chitoglucan 50, 150, or 300 mg/kg/day for 3 weeks (HFD + CG groups). The food consumption, body weight, fat contents, and the levels of serum leptin and resistin were assessed after treatment of chitoglucan. Results: the HFD produced a marked increase in body and fat weights after 6 weeks of feeding compared with the Normal group. Administration of chitoglucan for 3 weeks tended to reduce body weight and significantly decreased parametrical adipose tissues in HFD groups. The level of serum leptin in the HFD group was markedly higher than that in the Normal group, whereas the level of leptin in the chitoglucan treated groups was significantly decreased in comparison with the HFD group. In addition, the level of serum resistin in high-fat diet group tended to be more increased than Normal group. However, the serum resistin level was significantly reduced in HF diet groups after treatment with chitoglucan (50 mg/kg or 150 mg/kg). Conclusion: Collectively, these data suggest that chitoglucan from the Flammulina velutipes may be useful in the treatment of high diet-induced obesity and metabolic syndrome. |
format | Online Article Text |
id | pubmed-9819012 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-98190122023-01-07 Anti-Obesity Effect of Chitoglucan in High-Fat-Induced Obesity Mice Park, Hyun-Jung Lee, SunYoung Ye, Minsook Han, Bong Hee Shim, Hyun Soo Jang, Daehyuk Shim, Insop Int J Environ Res Public Health Article Background: Chitoglucan (CG) is a bioactive component obtained from Flammulina velutipes Sing, an edible mushroom, which is known to have an anti-obesity effect. However, its biological and hormonal activities in alleviating obesity through regulation of adipocyte-derived proteins have not been examined yet. Purpose: The present study aimed to investigate the anti-obesity effects of chitoglucan and its hormonal mechanisms in high-fat diet (HFD)-induced mice. Methods: The mice were fed either a normal diet (Normal group) or a high fat diet (HFD group) over 6 weeks. The HFD fed mice were administered with saline (HFD group), adipex (HFD + adipex group), chitoglucan 50, 150, or 300 mg/kg/day for 3 weeks (HFD + CG groups). The food consumption, body weight, fat contents, and the levels of serum leptin and resistin were assessed after treatment of chitoglucan. Results: the HFD produced a marked increase in body and fat weights after 6 weeks of feeding compared with the Normal group. Administration of chitoglucan for 3 weeks tended to reduce body weight and significantly decreased parametrical adipose tissues in HFD groups. The level of serum leptin in the HFD group was markedly higher than that in the Normal group, whereas the level of leptin in the chitoglucan treated groups was significantly decreased in comparison with the HFD group. In addition, the level of serum resistin in high-fat diet group tended to be more increased than Normal group. However, the serum resistin level was significantly reduced in HF diet groups after treatment with chitoglucan (50 mg/kg or 150 mg/kg). Conclusion: Collectively, these data suggest that chitoglucan from the Flammulina velutipes may be useful in the treatment of high diet-induced obesity and metabolic syndrome. MDPI 2022-12-24 /pmc/articles/PMC9819012/ /pubmed/36612600 http://dx.doi.org/10.3390/ijerph20010281 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 | Article Park, Hyun-Jung Lee, SunYoung Ye, Minsook Han, Bong Hee Shim, Hyun Soo Jang, Daehyuk Shim, Insop Anti-Obesity Effect of Chitoglucan in High-Fat-Induced Obesity Mice |
title | Anti-Obesity Effect of Chitoglucan in High-Fat-Induced Obesity Mice |
title_full | Anti-Obesity Effect of Chitoglucan in High-Fat-Induced Obesity Mice |
title_fullStr | Anti-Obesity Effect of Chitoglucan in High-Fat-Induced Obesity Mice |
title_full_unstemmed | Anti-Obesity Effect of Chitoglucan in High-Fat-Induced Obesity Mice |
title_short | Anti-Obesity Effect of Chitoglucan in High-Fat-Induced Obesity Mice |
title_sort | anti-obesity effect of chitoglucan in high-fat-induced obesity mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9819012/ https://www.ncbi.nlm.nih.gov/pubmed/36612600 http://dx.doi.org/10.3390/ijerph20010281 |
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