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Combretum lanceolatum flowers ethanol extract inhibits hepatic gluconeogenesis: an in vivo mechanism study

dc.contributor.authorSiqueira, Juliany Torres
dc.contributor.authorBatistela, Emanuele
dc.contributor.authorPereira, Mayara Peron
dc.contributor.authorda Silva, Virginia Claudia
dc.contributor.authorde Sousa Junior, Paulo Teixeira
dc.contributor.authorAndrade, Claudia Marlise Balbinotti
dc.contributor.authorKawashita, Nair Honda
dc.contributor.authorBertolini, Gisele Lopes
dc.contributor.authorBaviera, Amanda Martins [UNESP]
dc.contributor.institutionFederal University of Mato Grosso
dc.contributor.institutionUniversidade Estadual de Londrina (UEL)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2018-12-11T17:00:49Z
dc.date.available2018-12-11T17:00:49Z
dc.date.issued2016-09-01
dc.description.abstractContext Ethnopharmacological studies have demonstrated that plants of the Combretum genus presented antidiabetic activity, including Combretum lanceolatum Pohl ex Eichler (Combretaceae). Objective This study investigated the hepatic mechanisms of action of C. lanceolatum flowers ethanol extract (ClEtOH) related to its antihyperglycaemic effect in streptozotocin-diabetic rats. Materials and methods Male Wistar rats were divided into normal (N) and diabetic control (DC) rats treated with vehicle (water); diabetic rats treated with 500 mg/kg metformin (DMet) or 500 mg/kg ClEtOH (DT500). After 21 d of treatment, hepatic glucose and urea production were investigated through in situ perfused liver with l-glutamine. Changes in the phosphoenolpyruvate carboxykinase (PEPCK) levels and in the activation of adenosine monophosphate-activated protein kinase (AMPK) and insulin-signalling intermediates were also investigated. Results Similar to DMet, DT500 rats showed a reduction in the rates of hepatic production of glucose (46%) and urea (22%) in comparison with DC. This reduction was accompanied by a reduction in the PEPCK levels in liver of DT500 (28%) and DMet (43%) when compared with DC. AMPK phosphorylation levels were higher in the liver of DT500 (17%) and DMet (16%) rats. The basal AKT phosphorylation levels were increased in liver of DT500 rats, without differences in the insulin-stimulated AKT phosphorylation and in the insulin receptor levels between DC and DT500 rats. Discussion and conclusion The antidiabetic activity of ClEtOH can be attributed, at least in part, to inhibition of hepatic gluconeogenesis, probably due to the activation of both AMPK and AKT effectors and reduction in the PEPCK levels.en
dc.description.affiliationDepartment of Chemistry Federal University of Mato Grosso
dc.description.affiliationDepartment of Physiological Sciences State University of Londrina
dc.description.affiliationDepartment of Clinical Analysis School of Pharmaceutical Sciences São Paulo State University UNESP
dc.description.affiliationUnespDepartment of Clinical Analysis School of Pharmaceutical Sciences São Paulo State University UNESP
dc.format.extent1671-1679
dc.identifierhttp://dx.doi.org/10.3109/13880209.2015.1120321
dc.identifier.citationPharmaceutical Biology, v. 54, n. 9, p. 1671-1679, 2016.
dc.identifier.doi10.3109/13880209.2015.1120321
dc.identifier.file2-s2.0-84958061291.pdf
dc.identifier.issn1744-5116
dc.identifier.issn1388-0209
dc.identifier.scopus2-s2.0-84958061291
dc.identifier.urihttp://hdl.handle.net/11449/172529
dc.language.isoeng
dc.relation.ispartofPharmaceutical Biology
dc.relation.ispartofsjr0,563
dc.relation.ispartofsjr0,563
dc.rights.accessRightsAcesso abertopt
dc.sourceScopus
dc.subjectAntidiabetic activity
dc.subjectglucose hepatic production
dc.subjectphosphoenolpyruvate carboxykinase
dc.titleCombretum lanceolatum flowers ethanol extract inhibits hepatic gluconeogenesis: an in vivo mechanism studyen
dc.typeArtigopt
dspace.entity.typePublication
relation.isDepartmentOfPublicationa83d26d6-5383-42e4-bb3c-2678a6ddc144
relation.isDepartmentOfPublication.latestForDiscoverya83d26d6-5383-42e4-bb3c-2678a6ddc144
unesp.author.lattes3736475025187750[9]
unesp.author.orcid0000-0003-0987-5295[9]
unesp.departmentAnálises Clínicas - FCFpt

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