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Crocin-I Protects Against High-Fat Diet-Induced Obesity via Modulation of Gut Microbiota and Intestinal Inflammation in Mice

Crocin-I can regulate physiological changes in the human body by altering inflammation and microbial composition. Gut microbiota are also involved in modulating the pathophysiology of obesity. However, crocin-I’s effect on obesity and the mechanism underlying its effects on gut microbiota and inflam...

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Autores principales: Xie, Xiaoxian, Zhang, Mengya, Sun, Lei, Wang, Ting, Zhu, Zhengyan, Shu, Ruonan, Wu, Fengchun, Li, Zezhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9403484/
https://www.ncbi.nlm.nih.gov/pubmed/36034852
http://dx.doi.org/10.3389/fphar.2022.894089
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author Xie, Xiaoxian
Zhang, Mengya
Sun, Lei
Wang, Ting
Zhu, Zhengyan
Shu, Ruonan
Wu, Fengchun
Li, Zezhi
author_facet Xie, Xiaoxian
Zhang, Mengya
Sun, Lei
Wang, Ting
Zhu, Zhengyan
Shu, Ruonan
Wu, Fengchun
Li, Zezhi
author_sort Xie, Xiaoxian
collection PubMed
description Crocin-I can regulate physiological changes in the human body by altering inflammation and microbial composition. Gut microbiota are also involved in modulating the pathophysiology of obesity. However, crocin-I’s effect on obesity and the mechanism underlying its effects on gut microbiota and inflammation remain poorly understood. Here, high-fat diet (HFD) -induced obese mice were administrated crocin-I (20 mg/kg/day) for 10 weeks using an oral gavage (HFD-C20 group). HFD-C20, HFD, and Normal chow (NC) groups were compared. The fat content, colon tissue inflammatory cytokine levels, gut microbiota, and short-chain fatty acids (SCFAs) levels were measured. We show that crocin-I reduced body weight and liver weight and improved glucose resistance in HFD-induced mice, and reduced the lipid accumulation in the liver. Strikingly, crocin-I alleviated intestinal microbial disorders and decreased the F/B ratio and the abundance of Proteobacteria in HFD-induced obese mice. Crocin-I also rescued the decrease in the levels of SCFAs and repaired altered intestinal barrier functioning and intestinal inflammation in HFD-induced obese mice. These findings indicate that crocin-I may inhibit obesity by modulating the composition of gut microbiota and intestinal inflammation.
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spelling pubmed-94034842022-08-26 Crocin-I Protects Against High-Fat Diet-Induced Obesity via Modulation of Gut Microbiota and Intestinal Inflammation in Mice Xie, Xiaoxian Zhang, Mengya Sun, Lei Wang, Ting Zhu, Zhengyan Shu, Ruonan Wu, Fengchun Li, Zezhi Front Pharmacol Pharmacology Crocin-I can regulate physiological changes in the human body by altering inflammation and microbial composition. Gut microbiota are also involved in modulating the pathophysiology of obesity. However, crocin-I’s effect on obesity and the mechanism underlying its effects on gut microbiota and inflammation remain poorly understood. Here, high-fat diet (HFD) -induced obese mice were administrated crocin-I (20 mg/kg/day) for 10 weeks using an oral gavage (HFD-C20 group). HFD-C20, HFD, and Normal chow (NC) groups were compared. The fat content, colon tissue inflammatory cytokine levels, gut microbiota, and short-chain fatty acids (SCFAs) levels were measured. We show that crocin-I reduced body weight and liver weight and improved glucose resistance in HFD-induced mice, and reduced the lipid accumulation in the liver. Strikingly, crocin-I alleviated intestinal microbial disorders and decreased the F/B ratio and the abundance of Proteobacteria in HFD-induced obese mice. Crocin-I also rescued the decrease in the levels of SCFAs and repaired altered intestinal barrier functioning and intestinal inflammation in HFD-induced obese mice. These findings indicate that crocin-I may inhibit obesity by modulating the composition of gut microbiota and intestinal inflammation. Frontiers Media S.A. 2022-08-11 /pmc/articles/PMC9403484/ /pubmed/36034852 http://dx.doi.org/10.3389/fphar.2022.894089 Text en Copyright © 2022 Xie, Zhang, Sun, Wang, Zhu, Shu, Wu and Li. 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 Pharmacology
Xie, Xiaoxian
Zhang, Mengya
Sun, Lei
Wang, Ting
Zhu, Zhengyan
Shu, Ruonan
Wu, Fengchun
Li, Zezhi
Crocin-I Protects Against High-Fat Diet-Induced Obesity via Modulation of Gut Microbiota and Intestinal Inflammation in Mice
title Crocin-I Protects Against High-Fat Diet-Induced Obesity via Modulation of Gut Microbiota and Intestinal Inflammation in Mice
title_full Crocin-I Protects Against High-Fat Diet-Induced Obesity via Modulation of Gut Microbiota and Intestinal Inflammation in Mice
title_fullStr Crocin-I Protects Against High-Fat Diet-Induced Obesity via Modulation of Gut Microbiota and Intestinal Inflammation in Mice
title_full_unstemmed Crocin-I Protects Against High-Fat Diet-Induced Obesity via Modulation of Gut Microbiota and Intestinal Inflammation in Mice
title_short Crocin-I Protects Against High-Fat Diet-Induced Obesity via Modulation of Gut Microbiota and Intestinal Inflammation in Mice
title_sort crocin-i protects against high-fat diet-induced obesity via modulation of gut microbiota and intestinal inflammation in mice
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9403484/
https://www.ncbi.nlm.nih.gov/pubmed/36034852
http://dx.doi.org/10.3389/fphar.2022.894089
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