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Article: Gut microbiota-bile acid crosstalk contributes to the rebound weight gain after calorie restriction in mice

TitleGut microbiota-bile acid crosstalk contributes to the rebound weight gain after calorie restriction in mice
Authors
Issue Date2022
Citation
Nature Communications, 2022, v. 13, n. 1, article no. 2060 How to Cite?
AbstractCalorie restriction (CR) and fasting are common approaches to weight reduction, but the maintenance is difficult after resuming food consumption. Meanwhile, the gut microbiome associated with energy harvest alters dramatically in response to nutrient deprivation. Here, we reported that CR and high-fat diet (HFD) both remodeled the gut microbiota with similar microbial composition, Parabacteroides distasonis was most significantly decreased after CR or HFD. CR altered microbiota and reprogramed metabolism, resulting in a distinct serum bile acid profile characterized by depleting the proportion of non-12α-hydroxylated bile acids, ursodeoxycholic acid and lithocholic acid. Downregulation of UCP1 expression in brown adipose tissue and decreased serum GLP-1 were observed in the weight-rebound mice. Moreover, treatment with Parabacteroides distasonis or non-12α-hydroxylated bile acids ameliorated weight regain via increased thermogenesis. Our results highlighted the gut microbiota-bile acid crosstalk in rebound weight gain and Parabacteroides distasonis as a potential probiotic to prevent rapid post-CR weight gain.
Persistent Identifierhttp://hdl.handle.net/10722/342650
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLi, Mengci-
dc.contributor.authorWang, Shouli-
dc.contributor.authorLi, Yitao-
dc.contributor.authorZhao, Mingliang-
dc.contributor.authorKuang, Junliang-
dc.contributor.authorLiang, Dandan-
dc.contributor.authorWang, Jieyi-
dc.contributor.authorWei, Meilin-
dc.contributor.authorRajani, Cynthia-
dc.contributor.authorMa, Xinran-
dc.contributor.authorTang, Yajun-
dc.contributor.authorRen, Zhenxing-
dc.contributor.authorChen, Tianlu-
dc.contributor.authorZhao, Aihua-
dc.contributor.authorHu, Cheng-
dc.contributor.authorShen, Chengxing-
dc.contributor.authorJia, Weiping-
dc.contributor.authorLiu, Ping-
dc.contributor.authorZheng, Xiaojiao-
dc.contributor.authorJia, Wei-
dc.date.accessioned2024-04-17T07:05:17Z-
dc.date.available2024-04-17T07:05:17Z-
dc.date.issued2022-
dc.identifier.citationNature Communications, 2022, v. 13, n. 1, article no. 2060-
dc.identifier.urihttp://hdl.handle.net/10722/342650-
dc.description.abstractCalorie restriction (CR) and fasting are common approaches to weight reduction, but the maintenance is difficult after resuming food consumption. Meanwhile, the gut microbiome associated with energy harvest alters dramatically in response to nutrient deprivation. Here, we reported that CR and high-fat diet (HFD) both remodeled the gut microbiota with similar microbial composition, Parabacteroides distasonis was most significantly decreased after CR or HFD. CR altered microbiota and reprogramed metabolism, resulting in a distinct serum bile acid profile characterized by depleting the proportion of non-12α-hydroxylated bile acids, ursodeoxycholic acid and lithocholic acid. Downregulation of UCP1 expression in brown adipose tissue and decreased serum GLP-1 were observed in the weight-rebound mice. Moreover, treatment with Parabacteroides distasonis or non-12α-hydroxylated bile acids ameliorated weight regain via increased thermogenesis. Our results highlighted the gut microbiota-bile acid crosstalk in rebound weight gain and Parabacteroides distasonis as a potential probiotic to prevent rapid post-CR weight gain.-
dc.languageeng-
dc.relation.ispartofNature Communications-
dc.titleGut microbiota-bile acid crosstalk contributes to the rebound weight gain after calorie restriction in mice-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1038/s41467-022-29589-7-
dc.identifier.pmid35440584-
dc.identifier.scopuseid_2-s2.0-85128348411-
dc.identifier.volume13-
dc.identifier.issue1-
dc.identifier.spagearticle no. 2060-
dc.identifier.epagearticle no. 2060-
dc.identifier.eissn2041-1723-
dc.identifier.isiWOS:000784997300044-

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