Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/112254
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dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.creatorLiu, T-
dc.creatorLei, C-
dc.creatorHuang, Q-
dc.creatorSong, W-
dc.creatorLi, C-
dc.creatorSun, N-
dc.creatorLiu, Z-
dc.date.accessioned2025-04-08T00:43:41Z-
dc.date.available2025-04-08T00:43:41Z-
dc.identifier.urihttp://hdl.handle.net/10397/112254-
dc.language.isoenen_US
dc.publisherDove Medical Press Ltd.en_US
dc.rights© 2024 Liu et al. This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).en_US
dc.rightsThe following publication Liu T, Lei C, Huang Q, Song W, Li C, Sun N, Liu Z. Hesperidin and Fecal Microbiota Transplantation Modulate the Composition of the Gut Microbiota and Reduce Obesity in High Fat Diet Mice. Diabetes Metab Syndr Obes. 2024;17:3643-3656 is available at https://dx.doi.org/10.2147/DMSO.S474034.en_US
dc.subjectFecal microbiota transplantationen_US
dc.subjectGut microbiotaen_US
dc.subjectHesperidinen_US
dc.subjectHigh-fat dieten_US
dc.subjectObesityen_US
dc.titleHesperidin and fecal microbiota transplantation modulate the composition of the gut microbiota and reduce obesity in high fat diet miceen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage3643-
dc.identifier.epage3656-
dc.identifier.volume17-
dc.identifier.doi10.2147/DMSO.S474034-
dcterms.abstractIntroduction: Obesity, which is associated with gut microbiota dysbiosis, low-grade chronic inflammation and intestinal barrier dysfunction, can cause a variety of chronic metabolic diseases. Phytochemical flavonoids have a variety of biological activities, among which there may be safe and effective anti-obesity solutions.-
dcterms.abstractMethods: We tested a plant-derived flavonoid hesperidin and fecal microbiota transplantation (FMT) to alleviate diet-induced obesity. High-fat diet (HFD)-fed mice were treated with hesperidin (100 and 200 mg/kg BW) and FMT.-
dcterms.abstractResults: Results indicated that hesperidin had the effects of reducing obesity as indicated by reduction of body weight, fat accumulation and blood lipids, reducing inflammation as indicated by reduction of pro-inflammation factors including TNFα, IL-6, IL-1βand iNOS, and improving gut integrity as indicated by increasing colon length, reducing plasma gut permeability indicators iFABP and LBP, increased mRNA expression of mucus protein Muc2, tight junction p Claudin 2, Occludin and ZO-1 in the HFD-fed mice. The anti-obesity effects of hesperidin treatment have a dose-dependent manner. In addition, 16S rRNA-based gut microbiota analysis revealed that hesperidin selectively promoted the growth of Lactobacillus salivarius, Staphylococcus sciuri and Desulfovibrio C21_c20 while inhibiting Bifidobacterium pseudolongum, Mucispirillum schaedleri, Helicobacter ganmani and Helicobacter hepaticus in the HFD-fed mice. Horizontal feces transfer from the normal diet (ND)-fed mice to the HFD-fed mice conferred anti-obesity effects and transmitted some of the HFD-modulated microbes.-
dcterms.abstractConclusion: We concluded that hesperidin and FMT both affect the reduction of body weight and improve HFD-related disorders in the HFD-fed mice possibly through modulating the composition of the gut microbiota.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationDiabetes, metabolic syndrome and obesity , 2024, v. 17, p. 3643-3656-
dcterms.isPartOfDiabetes, metabolic syndrome and obesity-
dcterms.issued2024-
dc.identifier.scopus2-s2.0-85207500912-
dc.identifier.eissn1178-7007-
dc.description.validate202504 bcrc-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOSen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNational Natural Science Foundation of China; Guangzhou Science and Technology Plan Joint Foundation of City and University; University-Industry Cooperation Innovation Foundation of Science and Technology Development Center of the Ministry of Education of China; Key Laboratory of Guangdong Higher Education Institutes; Guangzhou Workstation Open Project of State Key Laboratory of Dampness Syndrome of Chinese Medicineen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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