Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/117766
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dc.contributorDepartment of Food Science and Nutrition-
dc.creatorCheng, CK-
dc.creatorYe, L-
dc.creatorWang, Y-
dc.creatorWang, YL-
dc.creatorXia, Y-
dc.creatorWong, SHS-
dc.creatorChen, S-
dc.creatorHuang, Y-
dc.date.accessioned2026-03-05T07:56:16Z-
dc.date.available2026-03-05T07:56:16Z-
dc.identifier.issn2095-2546-
dc.identifier.urihttp://hdl.handle.net/10397/117766-
dc.language.isoenen_US
dc.publisherShanghai University of Sporten_US
dc.rights© 2025 Published by Elsevier B.V. on behalf of Shanghai University of Sport. This is an open access article under the CC BY-NC-ND license. (http://creativecommons.org/licenses/by-nc-nd/4.0/)en_US
dc.rightsThe following publication Cheng, C. K., Ye, L., Wang, Y., Wang, Y.-L., Xia, Y., Wong, S. H.-S., Chen, S., & Huang, Y. (2025). Exercised gut microbiota improves vascular and metabolic abnormalities in sedentary diabetic mice through gut‒vascular connection. Journal of Sport and Health Science, 14, 101026 is available at https://doi.org/10.1016/j.jshs.2025.101026.en_US
dc.subjectDiabetes mellitusen_US
dc.subjectEndothelial dysfunctionen_US
dc.subjectExerciseen_US
dc.subjectFecal microbiota transplantationen_US
dc.subjectMicroRNAen_US
dc.titleExercised gut microbiota improves vascular and metabolic abnormalities in sedentary diabetic mice through gut-vascular connectionen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume14-
dc.identifier.doi10.1016/j.jshs.2025.101026-
dcterms.abstractBackground: Exercise elicits cardiometabolic benefits, reducing the risks of cardiovascular diseases and type 2 diabetes. This study aimed to investigate the vascular and metabolic effects of gut microbiota from exercise-trained donors on sedentary mice with type 2 diabetes and the potential mechanism.-
dcterms.abstractMethods: Leptin receptor-deficient diabetic (db/db) and nondiabetic (db/m+) mice underwent running treadmill exercise for 8 weeks, during which fecal microbiota transplantation (FMT) was parallelly performed from exercise-trained to sedentary diabetic (db/db) mice. Endothelial function, glucose homeostasis, physical performance, and vascular signaling of recipient mice were assessed. Vascular and intestinal stresses, including inflammation, oxidative stress, and endoplasmic reticulum (ER) stress, were investigated. RNA sequencing analysis on mouse aortic and intestinal tissues was performed. Gut microbiota profiles of recipient mice were evaluated by metagenomic sequencing.-
dcterms.abstractResults: Chronic exercise improved vascular and metabolic abnormalities in donor mice. Likewise, FMT from exercised donors retarded body weight gain and slightly improved grip strength and rotarod performance in recipient mice. Exercise-associated FMT enhanced endothelial function in different arteries, suppressed vascular and intestinal stresses, and improved glucose homeostasis in recipient mice, with noted microRNA–181b upregulation in aortas and intestines. Altered gut microbiota profiles and gut-derived factors (e.g., short-chain fatty acids and glucagon-like peptide-1) as well as improved intestinal integrity shall contribute to the cardiometabolic benefits, implying a gut‒vascular connection.-
dcterms.abstractConclusion: This proof-of-concept study indicates that exercised microbiota confers cardiometabolic benefits on sedentary db/db mice, extending the beneficial mechanism of exercise through gut‒vascular communication. The findings open up new therapeutic opportunities for cardiometabolic diseases and shed light on the development of exercise mimetics by targeting the gut microbiota.-
dcterms.abstractGraphical abstract: [Figure not available: see fulltext.]-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationJournal of sport and health science, Dec. 2025, v. 14, 101026-
dcterms.isPartOfJournal of sport and health science-
dcterms.issued2025-12-
dc.identifier.scopus2-s2.0-86000758438-
dc.identifier.pmid39827989-
dc.identifier.eissn2213-2961-
dc.identifier.artn101026-
dc.description.validate202603 bcch-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOSen_US
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThis study was funded by the Health and Medical Research Fund (Grant No. 08190776) and Hong Kong Research Grants Council (T12-101/23-N, SRFS2021-4S04 to Yu Huang, and T11-104/22-R to Sheng Chen). The work described in this paper was also substantially supported by a fellowship award from the Research Grants Council of the Hong Kong Special Administrative Region, China (Project No. CityU PDFS2223-1S01). We thank members of the Yu Huang group for the constructive discussions. Some figure panels were created with BioRender.com.en_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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