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Hypothermic effect of acute citral treatment during lps-induced systemic inflammation in obese mice: reduction of serum tnf-α and leptin levels

dc.contributor.authorEmílio-Silva, Maycon T. [UNESP]
dc.contributor.authorRodrigues, Vinicius P. [UNESP]
dc.contributor.authorBueno, Gabriela [UNESP]
dc.contributor.authorOhara, Rie [UNESP]
dc.contributor.authorMartins, Marina G.
dc.contributor.authorHorta-Júnior, José A. C. [UNESP]
dc.contributor.authorBranco, Luiz G. S.
dc.contributor.authorRocha, Lúcia R. M. [UNESP]
dc.contributor.authorHiruma-Lima, Clélia A. [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2021-06-25T10:13:30Z
dc.date.available2021-06-25T10:13:30Z
dc.date.issued2020-10-01
dc.description.abstractCitral is a mixture of monoterpenes present in the essential oil of several plants, such as Cymbopogon citratus and Zingiber officinale, possessing anti-inflammatory, anti-ulcerogenic, and antipyretic actions. We investigated the action of citral on body temperature (Tb) and inflammatory signaling in eutrophic and obese mice during Systemic Inflammation (SI) induced by Lipopolysaccharide (LPS). Thus, we assessed the effect of citral (25, 100, and 300 mg/kg) and ibuprofen in LPS-induced SI in Swiss male mice fed a standard diet (SD) or high-fat diet (HFD) for 12 weeks. Following SI induction, we measured Tb and collected the serum, hypothalamus, and gastric mucosa for biochemical measurements. Acute treatment with citral decreased the Tb of both SD and HFD-fed animals. Citral (300 mg/kg) treatment caused a significantly lower Tb variation in HFD-fed animals than in those fed the SD. Citral reduced peripheral levels of tumor necrosis factor (TNF)-α in SD and HFD mice and decreased serum leptin concentration in HFD mice 90 min after the LPS challenge. Furthermore, citral also reduced interleukin (IL)-6 levels in the hypothalamus of obese mice. In summary, citral effectively reduced Tb during SI by reducing inflammatory mediators with a distinct action profile in HFD mice when compared with SD.en
dc.description.affiliationDepartment of Structural and Functional Biology (Physiology) Institute of Biosciences São Paulo State University (UNESP)
dc.description.affiliationDepartment of Physiology Institute of Biosciences University of São Paulo (USP)
dc.description.affiliationDepartment of Structural and Functional Biology (Anatomy) Institute of Biosciences São Paulo State University (UNESP)
dc.description.affiliationDepartment of Basic and Oral Biology Dental School of Ribeirão Preto University of São Paulo (USP)
dc.description.affiliationUnespDepartment of Structural and Functional Biology (Physiology) Institute of Biosciences São Paulo State University (UNESP)
dc.description.affiliationUnespDepartment of Structural and Functional Biology (Anatomy) Institute of Biosciences São Paulo State University (UNESP)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 2016/13136-6
dc.description.sponsorshipIdFAPESP: 2018/09873-0
dc.description.sponsorshipIdFAPESP: 2018/10935-0
dc.format.extent1-18
dc.identifierhttp://dx.doi.org/10.3390/biom10101454
dc.identifier.citationBiomolecules, v. 10, n. 10, p. 1-18, 2020.
dc.identifier.dimensionspub.1131868378
dc.identifier.doi10.3390/biom10101454
dc.identifier.issn2218-273X
dc.identifier.lattes3814504901386844
dc.identifier.orcid0000-0002-8645-3777
dc.identifier.orcid0000-0003-4430-0016
dc.identifier.orcid0000-0001-5466-3414
dc.identifier.orcid0000-0002-1259-1472
dc.identifier.orcid0000-0003-3639-9861
dc.identifier.orcid0000-0003-0292-4947
dc.identifier.orcid0000-0002-9312-2431
dc.identifier.orcid0000-0002-7911-3862
dc.identifier.pmcidPMC7603063
dc.identifier.pmid33080865
dc.identifier.scopus2-s2.0-85092706238
dc.identifier.urihttp://hdl.handle.net/11449/205326
dc.language.isoeng
dc.publisherMDPI
dc.relation.ispartofBiomolecules
dc.rights.accessRightsAcesso abertopt
dc.rights.sourceRightsoa_all
dc.rights.sourceRightsgold
dc.sourceScopus
dc.sourceDimensions
dc.subjectCitral
dc.subjectLipopolysaccharide
dc.subjectMonoterpene
dc.subjectObesity
dc.subjectSystemic inflammation
dc.titleHypothermic effect of acute citral treatment during lps-induced systemic inflammation in obese mice: reduction of serum tnf-α and leptin levelsen
dc.typeArtigopt
dspace.entity.typePublication
unesp.author.lattes3814504901386844[9]
unesp.author.orcid0000-0002-8645-3777[9]

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