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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/69574
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dc.contributor.authorVentrucci, Gislaine-
dc.contributor.authorMello, Maria Alice R.-
dc.contributor.authorGomes-Marcondes, Maria Cristina C.-
dc.date.accessioned2014-05-27T11:22:26Z-
dc.date.accessioned2016-10-25T18:23:40Z-
dc.date.available2014-05-27T11:22:26Z-
dc.date.available2016-10-25T18:23:40Z-
dc.date.issued2007-03-06-
dc.identifierhttp://dx.doi.org/10.1186/1471-2407-7-42-
dc.identifier.citationBMC Cancer, v. 7.-
dc.identifier.issn1471-2407-
dc.identifier.urihttp://hdl.handle.net/11449/69574-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/69574-
dc.description.abstractBackground: Cancer-cachexia induces a variety of metabolic disorders on protein turnorver, decreasing protein synthesis and increasing protein degradation. Controversly, insulin, other hormones, and branched-chain amino acids, especially leucine, stimulate protein synthesis and modulate the activity of translation initiation factors involved in protein synthesis. Since the tumour effects are more pronounced when associated with pregnancy, ehancing muscle-wasting proteolysis, in this study, the influence of a leucine-rich diet on the protein synthesis caused by cancer were investigated. Methods: Pregnant rats with or without Walker 256 tumour were distributed into six groups. During 20 days of experiment, three groups were fed with a control diet: C - pregnant control, W - tumour-bearing, and P - pair-fed, which received the same amount of food as ingested by the W group; three other groups of pregnant rats were fed a leucine-rich diet: L - pregnant leucine, WL - tumour-bearing, and PL - pair-fed, which received the same amount of food as ingested by the WL group. Results: The gastrocnemius muscle of WL rats showed increased incorporation of leucine in protein compared to W rats; the leucine-rich diet also prevented the decrease in plasma insulin normally seen in W. The expression of translation initiation factors increased when tumour-bearing rats fed leucine-rich diet, with increase of ∼35% for eIF2α and eIF5, ∼17% for eIF4E and 20% for eIF4G; the expression of protein kinase S6K1 and protein kinase C was also highly enhanced. Conclusion: The results suggest that a leucine-rich diet increased the protein synthesis in skeletal muscle in tumour-bearing rats possibly through the activation of eIF factors and/or the S6kinase pathway. © 2007 Ventrucci et al; licensee BioMed Central Ltd.en
dc.language.isoeng-
dc.sourceScopus-
dc.subjectactin-
dc.subjectinitiation factor-
dc.subjectinitiation factor 2alpha-
dc.subjectinitiation factor 4E-
dc.subjectinitiation factor 4G-
dc.subjectinitiation factor 5-
dc.subjectinsulin-
dc.subjectleucine-
dc.subjectprotein kinase C-
dc.subjectserum and glucocorticoid regulated kinase 1-
dc.subjectanimal experiment-
dc.subjectanimal model-
dc.subjectanimal tissue-
dc.subjectcontrolled study-
dc.subjectdietary intake-
dc.subjectenzyme activation-
dc.subjectfemale-
dc.subjectgastrocnemius muscle-
dc.subjectinsulin blood level-
dc.subjectmale-
dc.subjectmalignant neoplastic disease-
dc.subjectnonhuman-
dc.subjectpregnancy-
dc.subjectprotein expression-
dc.subjectprotein synthesis-
dc.subjectrat-
dc.subjectskeletal muscle-
dc.titleLeucine-rich diet alters the eukaryotic translation initiation factors expression in skeletal muscle of tumour-bearing ratsen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationDepartamento de Fisiologia e Biofísica Instituto de Biologia Universidade Estadual de Campinas (UNICAMP), Campinas 13083-970 São Paulo-
dc.description.affiliationDepartamento de Fisiologia e Biofísica Instituto Biociências Universidade Estadual de São Paulo, Rio Claro 13506-900 São Paulo-
dc.description.affiliationUnespDepartamento de Fisiologia e Biofísica Instituto Biociências Universidade Estadual de São Paulo, Rio Claro 13506-900 São Paulo-
dc.identifier.doi10.1186/1471-2407-7-42-
dc.rights.accessRightsAcesso aberto-
dc.identifier.file2-s2.0-33947729996.pdf-
dc.relation.ispartofBMC Cancer-
dc.identifier.scopus2-s2.0-33947729996-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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