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BALB/c and C57BL/6 mouse strains influence gastric function outcomes with administration of cisplatin and dexamethasone

dc.contributor.authorGama, Loyane Almeida [UNESP]
dc.contributor.authorMachado, Mariana Pirani Rocha [UNESP]
dc.contributor.authorCorá, Luciana Aparecida
dc.contributor.authorBeckmann, Ana Paula Simões
dc.contributor.authorAlves, Wellington David Luz
dc.contributor.authorMiranda, José Ricardo de Arruda [UNESP]
dc.contributor.authorAmérico, Madileine Francely [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionUFMT
dc.contributor.institutionUNCISAL
dc.date.accessioned2025-04-29T20:15:37Z
dc.date.issued2023-01-01
dc.description.abstractOur aim was to evaluate the effects of cisplatin and dexamethasone alone and combined on gastric contractility and histomorphometry of BALB/c and C57BL/6 mice. BALB/c and C57BL/6 male mice (8-week-old) were randomly separated into: Control; Cisplatin (7.5 mg/Kg); Dexamethasone (2.0 mg/Kg); and Dexamethasone plus Cisplatin (2.0 mg/Kg of dexamethasone 1-hour prior to 7.5 mg/Kg of cisplatin). Drugs were administered intraperitoneally for three days. Body weight and food intake were evaluated on 2nd day. Alternating Current Biosusceptometry technique was employed to measure gastric contractions on 3rd day. Afterward, mice were killed for gastric histomorphometric analysis. Cisplatin decreased food intake and caused bradygastria in BALB/c mice; however, the amplitude of gastric contractions decreased in both BALB/c and C57BL/6. Dexamethasone and cisplatin combined restored the gastric frequency and food intake only in BALB/c, but drug combination reduced the gastric amplitude of contractions in both strains. Dexamethasone alone increased gastric mucosa thickness in C57BL/6 and decreased muscular thickness in BALB/c. In conclusion, the mouse strains presented differences in acute effects of cisplatin and dexamethasone alone and combined on gastric function. This reinforces the importance of choosing the appropriate mouse strain for studying the acute effects of drugs on the gastrointestinal tract.en
dc.description.affiliationInstitute of Biosciences São Paulo State University UNESP, SP
dc.description.affiliationInstitute of Biological Sciences and Health Federal University of Mato Grosso UFMT, MT
dc.description.affiliationIntegrative Sciences Center Alagoas State University of Health Sciences UNCISAL, AL
dc.description.affiliationUnespInstitute of Biosciences São Paulo State University UNESP, SP
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipIdCAPES: 001
dc.identifierhttp://dx.doi.org/10.1590/s2175-97902023e22718
dc.identifier.citationBrazilian Journal of Pharmaceutical Sciences, v. 59.
dc.identifier.doi10.1590/s2175-97902023e22718
dc.identifier.issn2175-9790
dc.identifier.issn1984-8250
dc.identifier.scopus2-s2.0-85169810367
dc.identifier.urihttps://hdl.handle.net/11449/309462
dc.language.isoeng
dc.relation.ispartofBrazilian Journal of Pharmaceutical Sciences
dc.sourceScopus
dc.subjectBALB/c
dc.subjectBradygastria
dc.subjectC57BL/6
dc.subjectGastric motility
dc.subjectStomach
dc.titleBALB/c and C57BL/6 mouse strains influence gastric function outcomes with administration of cisplatin and dexamethasoneen
dc.typeArtigopt
dspace.entity.typePublication
unesp.author.orcid0000-0001-8474-3765[7]

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