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Article: Calorie restriction and its impact on gut microbial composition and global metabolism

TitleCalorie restriction and its impact on gut microbial composition and global metabolism
Authors
Keywordscaloric restriction
gut microbiota
metabolome
Issue Date2018
Citation
Frontiers of Medicine, 2018, v. 12, n. 6, p. 634-644 How to Cite?
AbstractCalorie restriction (CR) is a dietary regimen that reduces calorie intake without incurring malnutrition or a reduction in essential nutrients. It has long been recognized as a natural strategy for promoting health, extending longevity, and prevents the development of metabolic and age-related diseases. In the present review, we focus on the general effect of CR on gut microbiota composition and global metabolism. We also propose mechanisms for its beneficial effect. Results showed that probiotic and butyrate-producing microbes increased their relative abundance, whereas proinflammatory strains exhibited suppressed relative abundance following CR. Analyses of the gut microbial and host metabolisms revealed that most host microbial co-metabolites were changed due to CR. Examples of dramatic CR-induced changes in host metabolism included a decrease in the rate of lipid biosynthesis and an increase in the rates of fatty acid catabolism, β-oxidation, glycogenolysis, and gluconeogenesis. The observed phenotypes and the further verification of the direct link between gut microbiota and metabolome may benefit patients that are at risk for developing metabolic disease. Thus, improved gut microbiota composition and metabolome are potential biomarkers for determining the effectiveness of dietary interventions for age-related and metabolic diseases.
Persistent Identifierhttp://hdl.handle.net/10722/342583
ISSN
2023 Impact Factor: 3.9
2023 SCImago Journal Rankings: 1.468
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorZheng, Xiaojiao-
dc.contributor.authorWang, Shouli-
dc.contributor.authorJia, Wei-
dc.date.accessioned2024-04-17T07:04:50Z-
dc.date.available2024-04-17T07:04:50Z-
dc.date.issued2018-
dc.identifier.citationFrontiers of Medicine, 2018, v. 12, n. 6, p. 634-644-
dc.identifier.issn2095-0217-
dc.identifier.urihttp://hdl.handle.net/10722/342583-
dc.description.abstractCalorie restriction (CR) is a dietary regimen that reduces calorie intake without incurring malnutrition or a reduction in essential nutrients. It has long been recognized as a natural strategy for promoting health, extending longevity, and prevents the development of metabolic and age-related diseases. In the present review, we focus on the general effect of CR on gut microbiota composition and global metabolism. We also propose mechanisms for its beneficial effect. Results showed that probiotic and butyrate-producing microbes increased their relative abundance, whereas proinflammatory strains exhibited suppressed relative abundance following CR. Analyses of the gut microbial and host metabolisms revealed that most host microbial co-metabolites were changed due to CR. Examples of dramatic CR-induced changes in host metabolism included a decrease in the rate of lipid biosynthesis and an increase in the rates of fatty acid catabolism, β-oxidation, glycogenolysis, and gluconeogenesis. The observed phenotypes and the further verification of the direct link between gut microbiota and metabolome may benefit patients that are at risk for developing metabolic disease. Thus, improved gut microbiota composition and metabolome are potential biomarkers for determining the effectiveness of dietary interventions for age-related and metabolic diseases.-
dc.languageeng-
dc.relation.ispartofFrontiers of Medicine-
dc.subjectcaloric restriction-
dc.subjectgut microbiota-
dc.subjectmetabolome-
dc.titleCalorie restriction and its impact on gut microbial composition and global metabolism-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1007/s11684-018-0670-8-
dc.identifier.pmid30446879-
dc.identifier.scopuseid_2-s2.0-85056717741-
dc.identifier.volume12-
dc.identifier.issue6-
dc.identifier.spage634-
dc.identifier.epage644-
dc.identifier.eissn2095-0225-
dc.identifier.isiWOS:000453348800004-

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