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Tremella fuciformis polysaccharide reduces obesity in high-fat diet-fed mice by modulation of gut microbiota

Obesity is a metabolic disease associated with gut microbiota and low-grade chronic inflammation. Tremella fuciformis is a medicinal and edible fungus; polysaccharide (TP) is the main active component, which has a variety of biological activities, such as hypoglycemic and hypolipidemic. However, the...

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Autores principales: He, Gang, Chen, Tangcong, Huang, Lifen, Zhang, Yiyuan, Feng, Yanjiao, Qu, Shaokui, Yin, Xiaojing, Liang, Li, Yan, Jun, Liu, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9760882/
https://www.ncbi.nlm.nih.gov/pubmed/36545204
http://dx.doi.org/10.3389/fmicb.2022.1073350
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author He, Gang
Chen, Tangcong
Huang, Lifen
Zhang, Yiyuan
Feng, Yanjiao
Qu, Shaokui
Yin, Xiaojing
Liang, Li
Yan, Jun
Liu, Wei
author_facet He, Gang
Chen, Tangcong
Huang, Lifen
Zhang, Yiyuan
Feng, Yanjiao
Qu, Shaokui
Yin, Xiaojing
Liang, Li
Yan, Jun
Liu, Wei
author_sort He, Gang
collection PubMed
description Obesity is a metabolic disease associated with gut microbiota and low-grade chronic inflammation. Tremella fuciformis is a medicinal and edible fungus; polysaccharide (TP) is the main active component, which has a variety of biological activities, such as hypoglycemic and hypolipidemic. However, the anti-obesity effects and potential mechanisms of TP have never been reported. This study was conducted to elucidate the inhibitory effect of TP on high-fat diet (HFD)-induced obesity in mice. Mice were split into five groups: normal chow diet (NCD) group, NCD_TP_H group, HFD group, HFD_TP_L group and HFD_TP_H group. Our study showed that TP inhibited high-fat diet-induced weight gain and fat accumulation in mice and reduced blood glucose, hyperlipidemia and inflammation. TP also improved gut microbiota disorders by reducing the Firmicutes/Bacteroidetes ratio and modulating the relative abundance of specific gut microbiota. We also found that the anti-obesity and gut microbiota-modulating effects of TP could be transferred to HFD-fed mice via faecal microbiota transplantation (FMT), confirming that the gut microbiota was one of the targets of TP for obesity inhibition. Further studies showed that TP increased the production of short-chain fatty acids and the secretion of intestinal hormones. Our studies showed that TP inhibited obesity by modulating inflammation and the microbe-gut-brain axis, providing a rationale for developing TP to treat obesity and its complications.
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spelling pubmed-97608822022-12-20 Tremella fuciformis polysaccharide reduces obesity in high-fat diet-fed mice by modulation of gut microbiota He, Gang Chen, Tangcong Huang, Lifen Zhang, Yiyuan Feng, Yanjiao Qu, Shaokui Yin, Xiaojing Liang, Li Yan, Jun Liu, Wei Front Microbiol Microbiology Obesity is a metabolic disease associated with gut microbiota and low-grade chronic inflammation. Tremella fuciformis is a medicinal and edible fungus; polysaccharide (TP) is the main active component, which has a variety of biological activities, such as hypoglycemic and hypolipidemic. However, the anti-obesity effects and potential mechanisms of TP have never been reported. This study was conducted to elucidate the inhibitory effect of TP on high-fat diet (HFD)-induced obesity in mice. Mice were split into five groups: normal chow diet (NCD) group, NCD_TP_H group, HFD group, HFD_TP_L group and HFD_TP_H group. Our study showed that TP inhibited high-fat diet-induced weight gain and fat accumulation in mice and reduced blood glucose, hyperlipidemia and inflammation. TP also improved gut microbiota disorders by reducing the Firmicutes/Bacteroidetes ratio and modulating the relative abundance of specific gut microbiota. We also found that the anti-obesity and gut microbiota-modulating effects of TP could be transferred to HFD-fed mice via faecal microbiota transplantation (FMT), confirming that the gut microbiota was one of the targets of TP for obesity inhibition. Further studies showed that TP increased the production of short-chain fatty acids and the secretion of intestinal hormones. Our studies showed that TP inhibited obesity by modulating inflammation and the microbe-gut-brain axis, providing a rationale for developing TP to treat obesity and its complications. Frontiers Media S.A. 2022-12-05 /pmc/articles/PMC9760882/ /pubmed/36545204 http://dx.doi.org/10.3389/fmicb.2022.1073350 Text en Copyright © 2022 He, Chen, Huang, Zhang, Feng, Qu, Yin, Liang, Yan and Liu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
He, Gang
Chen, Tangcong
Huang, Lifen
Zhang, Yiyuan
Feng, Yanjiao
Qu, Shaokui
Yin, Xiaojing
Liang, Li
Yan, Jun
Liu, Wei
Tremella fuciformis polysaccharide reduces obesity in high-fat diet-fed mice by modulation of gut microbiota
title Tremella fuciformis polysaccharide reduces obesity in high-fat diet-fed mice by modulation of gut microbiota
title_full Tremella fuciformis polysaccharide reduces obesity in high-fat diet-fed mice by modulation of gut microbiota
title_fullStr Tremella fuciformis polysaccharide reduces obesity in high-fat diet-fed mice by modulation of gut microbiota
title_full_unstemmed Tremella fuciformis polysaccharide reduces obesity in high-fat diet-fed mice by modulation of gut microbiota
title_short Tremella fuciformis polysaccharide reduces obesity in high-fat diet-fed mice by modulation of gut microbiota
title_sort tremella fuciformis polysaccharide reduces obesity in high-fat diet-fed mice by modulation of gut microbiota
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9760882/
https://www.ncbi.nlm.nih.gov/pubmed/36545204
http://dx.doi.org/10.3389/fmicb.2022.1073350
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