Endurance exercise training increases APPL1 expression and improves insulin signaling in the hepatic tissue of diet-induced obese mice, independently of weight loss


Autoria(s): Marinho, R.; Ropelle, E. R.; Cintra, D. E.; Souza, C. T. de; Silva, A. S. R. da; Bertoli, F. C.; Colantonio, E.; D'Almeida, V.; Pauli, J. R.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

03/10/2013

03/10/2013

01/07/2012

Resumo

Hepatic insulin resistance is the major contributor to fasting hyperglycemia in type 2 diabetes. The protein kinase Akt plays a central role in the suppression of gluconeogenesis involving forkhead box O1 (Foxo1) and peroxisome proliferator-activated receptor gamma co-activator 1 alpha (PGC-1a), and in the control of glycogen synthesis involving the glycogen synthase kinase beta (GSK3 beta) in the liver. It has been demonstrated that endosomal adaptor protein APPL1 interacts with Akt and blocks the association of Akt with its endogenous inhibitor, tribbles-related protein 3 (TRB3), improving the action of insulin in the liver. Here, we demonstrated that chronic exercise increased the basal levels and insulin-induced Akt serine phosphorylation in the liver of diet-induced obese mice. Endurance training was able to increase APPL1 expression and the interaction between APPL1 and Akt. Conversely, training reduced both TRB3 expression and TRB3 and Akt association. The positive effects of exercise on insulin action are reinforced by our findings that showed that trained mice presented an increase in Foxo1 phosphorylation and Foxo1/PGC-1a association, which was accompanied by a reduction in gluconeogenic gene expressions (PEPCK and G6Pase). Finally, exercised animals demonstrated increased at basal and insulin-induced GSK3 beta phosphorylation levels and glycogen content at 24?h after the last session of exercise. Our findings demonstrate that exercise increases insulin action, at least in part, through the enhancement of APPL1 and the reduction of TRB3 expression in the liver of obese mice, independently of weight loss. J. Cell. Physiol. 227: 29172926, 2012. (C) 2011 Wiley Periodicals, Inc.

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [2010/04290-5]

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico

Identificador

JOURNAL OF CELLULAR PHYSIOLOGY, MALDEN, v. 227, n. 7, pp. 2917-2926, JUL, 2012

0021-9541

http://www.producao.usp.br/handle/BDPI/34000

10.1002/jcp.23037

http://dx.doi.org/10.1002/jcp.23037

Idioma(s)

eng

Publicador

WILEY-BLACKWELL

MALDEN

Relação

Journal of Cellular Physiology

Direitos

restrictedAccess

Copyright WILEY-BLACKWELL

Palavras-Chave #TRANSCRIPTION FACTOR FKHR #HUMAN SKELETAL-MUSCLE #PHYSICAL-EXERCISE #COACTIVATOR PGC-1 #GLUCOSE #LIVER #GLUCONEOGENESIS #RESISTANCE #PHOSPHORYLATION #METABOLISM #CELL BIOLOGY #PHYSIOLOGY
Tipo

article

original article

publishedVersion