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dc.contributor.authorSantos, Juliana
dc.contributor.authorGotardo, Érica
dc.contributor.authorBrianti, Mitsue
dc.contributor.authorPiraee, Mahmood
dc.contributor.authorGambero, Alessandra
dc.contributor.authorRibeiro, Marcelo
dc.date.accessioned2025-04-09T18:27:29Z
dc.date.available2025-04-09T18:27:29Z
dc.date.issued2014
dc.identifier.urihttp://repositorio.sis.puc-campinas.edu.br/xmlui/handle/123456789/17787
dc.description.abstractWe aimed to evaluate the in vitro effects of yerba maté, YGD (a herbal preparation containing yerba maté, guarana and damiana), and resveratrol on adipogenesis. The anti-adipogenic effects of yerba mate, YGD, resveratrol and YGD + resveratrol and yerba mate + resveratrol combinations were evaluated in 3T3-L1 cells by Oil Red staining, cellular triglyceride content, and PCR quantitative array. The results demonstrated that all of the tested compounds inhibited adipogenesis. Yerba maté extract significantly down-regulated the expression of genes that play an important role in regulating adipogenesis, such as Adig, Axin, Cebpa, Fgf10, Lep, Lpl, and Pparγ2. In addition, these genes, YGD also repressed Bmp2, Ccnd1, Fasn, and Srebf1. Resveratrol also modulated the expression of Adig, Bmp2, Ccnd1, C/EBPα, Fasn, Fgf10, Lep, Lpl, and Pparγ2. Moreover, resveratrol repressed Cebpb, Cdk4, Fgf2, and Klf15. The yerba maté extract and YGD up-regulated the expression of genes involved in inhibiting adipogenesis, such as Dlk-1, Klf2, and Ucp1. Resveratrol also induced the expression of Klf2 and Ucp1. In addition resveratrol modulated the Ddit3, Foxo1, Sirt1, and Sirt2. The combined effects of these compounds on gene expression showed similar results observed from individual treatments. Our data indicates that the synergy between the compounds favors the inhibition of adipogenesis.pt_BR
dc.language.isoInglês
dc.publisherMDPI AGpt_BR
dc.rightsAcesso abertopt_BR
dc.subjectYerba maté
dc.subjectResveratrol
dc.subjectAdipogenesis
dc.titleEffects of Yerba maté, a plant extract formulation (“YGD”) and resveratrol in 3T3-L1 adipogenesispt_BR
dc.typeArtigopt_BR
dc.contributor.institutionPontifícia Universidade Católica de Campinas (PUC-Campinas)pt_BR
dc.identifier.doihttps://doi.org/10.3390/molecules191016909pt_BR
dc.identifier.lattes7165708428659026pt_BR


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