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A high-fat diet changes the interaction of the extracellular matrix, cytokines, and growth factors in gastric ulcer repair

dc.contributor.authorOhara, Rie [UNESP]
dc.contributor.authorDario, Felipe Lima [UNESP]
dc.contributor.authorEmílio-Silva, Maycon Tavares [UNESP]
dc.contributor.authorAssunção, Renata [UNESP]
dc.contributor.authorRodrigues, Vinícius Peixoto [UNESP]
dc.contributor.authorBueno, Gabriela [UNESP]
dc.contributor.authorRaimundo, Priscila Romano [UNESP]
dc.contributor.authorJustulin, Luis Antonio [UNESP]
dc.contributor.authorda Rocha, Lúcia Regina Machado [UNESP]
dc.contributor.authorHiruma-Lima, Clelia Akiko [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.date.accessioned2025-04-29T18:59:31Z
dc.date.issued2025-04-01
dc.description.abstractBackground: Obesity is characterized by persistent low-grade inflammation that alters the gastrointestinal system and healing process. The link between obesity and the prevalence of stomach ulcers has not yet been fully established. Aims: We investigated the healing features of gastric lesions in male Swiss mice fed a standard diet (SD) or high-fat diet (HFD) using morphometric, biochemical, and molecular parameters. Methods: After 12 weeks on different diets, the animals underwent acetic acid-induced stomach ulcer surgery. To evaluate healing patterns, the stomachs of the animals were studied at five post-induction times, including the early, middle, and late phases of healing (1, 3, 7, 10, and 14 days). Morphometric features, activity of matrix metalloproteinases 2 and 9 (MMP-2 and 9), and measurement of inflammatory and growth factors were investigated using multiplex immunoassays. Results: Compared with the SD group, the HFD group demonstrated slowing of the early healing process. During the initial phase of the healing process, the SD group had significantly higher levels of EGF, VEGF-A, and VEGF-D than the HFD group. In the intermediate phase, only the SD group showed a 70 % increase in the regeneration area compared with the initial phase of the procedure. In this phase, the SD group also had higher levels of MMP-9, VEGF-D, and HGF than the HFD group. Conclusions: HFD can have a negative impact on the healing process of gastric ulcers in animals by delaying repair in gastric tissue when compared with animals consuming SD.en
dc.description.affiliationDepartment of Structural and Functional Biology Physiology Sector Institute of Biosciences São Paulo State University (UNESP), Botucatu
dc.description.affiliationDepartment of Structural and Functional Biology Morphology Sector Institute of Biosciences São Paulo State University (UNESP), Botucatu
dc.description.affiliationUnespDepartment of Structural and Functional Biology Physiology Sector Institute of Biosciences São Paulo State University (UNESP), Botucatu
dc.description.affiliationUnespDepartment of Structural and Functional Biology Morphology Sector Institute of Biosciences São Paulo State University (UNESP), Botucatu
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 2018/09873-0
dc.description.sponsorshipIdFAPESP: 2020/07384-2
dc.description.sponsorshipIdFAPESP: 2020/15225-1
dc.identifierhttp://dx.doi.org/10.1016/j.bbrc.2025.151565
dc.identifier.citationBiochemical and Biophysical Research Communications, v. 755.
dc.identifier.doi10.1016/j.bbrc.2025.151565
dc.identifier.issn1090-2104
dc.identifier.issn0006-291X
dc.identifier.scopus2-s2.0-85219237803
dc.identifier.urihttps://hdl.handle.net/11449/301838
dc.language.isoeng
dc.relation.ispartofBiochemical and Biophysical Research Communications
dc.sourceScopus
dc.subjectGastric ulcers
dc.subjectGrowth factors
dc.subjectHigh-fat diet
dc.subjectMatrix metalloproteinases
dc.subjectObesity
dc.titleA high-fat diet changes the interaction of the extracellular matrix, cytokines, and growth factors in gastric ulcer repairen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublicationab63624f-c491-4ac7-bd2c-767f17ac838d
relation.isOrgUnitOfPublication.latestForDiscoveryab63624f-c491-4ac7-bd2c-767f17ac838d
unesp.author.orcid0000-0003-4430-0016[1]
unesp.author.orcid0000-0002-1957-6152[2]
unesp.author.orcid0000-0001-5466-3414[3]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Botucatupt

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