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ARTIGO_GQ16NovelPeroxisome.pdf2,69 MBAdobe PDFVisualizar/Abrir
Título : GQ-16, a novel peroxisome proliferator-activated receptor (PPAR ) ligand, promotes insulin sensitization without weight gain
Autor : Amato, Angélica Amorim
Rajagopalan, Senapathy
Lin, Jean Z.
Carvalho, Bruno de Melo
Figueira, Ana Carolina Migliorini
Lu, Jenny
Ayers, Stephen D.
Mottin, Melina
Silveira, Rodrigo Leandro
Souza, Paulo Cesar Telles de
Mourão, Rosa Helena Veras
Saad, Mário José Abdalla
Togashi, Marie
Simeoni, Luiz Alberto
Abdalla, Dulcineia Saes Parra
Skaf, Munir Salomao
Polikarpov, Igor
Lima, Maria do Carmo Alves de
Galdino, Suely Lins
Brennan, Richard G.
Baxter, John Darling
Pitta, Ivan da Rocha
Webb, Paul
Phillips, Kevin J.
Neves, Francisco de Assis Rocha
Assunto:: Resistência à insulina
Diabetes
Medicamentos - uso terapêutico
Ganho/Perda de peso
Fecha de publicación : 10-ago-2012
Editorial : The American Society for Biochemistry and Molecular Biology, Inc.
Citación : AMATO, Angélica A. et al. GQ-16, a novel peroxisome proliferator-activated receptor (PPAR) ligand, promotes insulin sensitization without weight gain. The Journal of Biological Chemistry, v. 287, n. 33, p. 28169-28179, ago. 2012. Disponível em: <http://www.jbc.org/content/287/33/28169.full.pdf+html?sid=05080e27-cfc7-48aa-abf6-c1149dbce8ed>. Acesso em: 17 maio 2013.
Resumen : ABSTRACT
Background: PPAR agonists improve insulin sensitivity but also evoke weight gain. Results: GQ-16 is a PPAR partial agonist that blocks receptor phosphorylation by Cdk5 and improves insulin sensitivity in diabetic mice in the absence of weight gain. Conclusion: The unique binding mode of GQ-16 appears to be responsible for the compound’s advantageous pharmacological profile. Significance: Similar compounds could have promise as anti-diabetic therapeutics.
Licença:: The Journal of Biological Chemistry - The final version of the manuscript will be covered under the Creative Commons Attribution license (CC BY), the most accommodating of licenses offered. Click here for details.The final version of the manuscript will be released immediately on the publisher’s website and PubMed Central. Fonte: http://www.jbc.org/site/misc/Copyright_Permission.xhtml
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