Prolonged exposure to palmitate impairs fatty acid oxidation despite activation of AMP-activated protein kinase in skeletal muscle cells


Autoria(s): PIMENTA, A. S.; GAIDHU, M. P.; HABIB, S.; SO, M.; FEDIUC, S.; MIRPOURIAN, M.; MUSHEEV, M.; Curi, Rui; CEDDIA, R. B.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2008

Resumo

The aim of this study was to investigate the chronic effects of palmitate on fatty acid (FA) oxidation, AMPK/ACC phosphorylation/activation, intracellular lipid accumulation, and the molecular Mechanisms involved in these processes in skeletal muscle cells. Exposure of L6 myotubes for 8 h to 200, 400, 600, and 800 mu M of palmitate did rot affect cel viability but significantly reduced FA oxidation by similar to 26.5%, similar to 43.5%, similar to 50%, and similar to 47%, respectively. Interestingly, this occurred despite significant increases in AMPK (similar to 2.5-fold) and ACC (similar to 3-fold) phosphorylation and in malonyl-CoA decarboxylase activity (similar to 38-60%). Low concentrations of palmitate (50-100 mu M) caused an increase (similar to 30%) in CPT-I activity. However, as the concentration of palmitate increased, CPT-I activity decreased by similar to 32% after exposure for 8 h to 800 mu M of palmitate. Although FA uptake was reduced (similar to 35%) in cells exposed to increasing, palmitate concentrations, intracellular lipid accumulation increased in a dose-dependent manner, reaching values similar to 2.3-, similar to 3-, and 4-fold higher than control in muscle cells exposed to 400, 600, and 800 mu M palmitate, respectively. Interestingly, myotubes exposed to 400 mu M of palmitate for 1h increased basal glucose uptake and glycogen synthesis by similar to 40%. However, as time of incubation in the presence of palmitate progressed from 1 to 8h, these increases were abolished and a time-dependent inhibition of insulin-stimulated glucose uptake (similar to 65%) and glycogen synthesis (30%) was observed in myotubes. These findings may help explain the dysfunctional adaptations that occur in glucose and FA Metabolism in skeletal muscle under conditions of chronically elevated circulating levels of non-esterified FAs. Such as in obesity and Type 2 Diabetes.

National Science and Engineering Research Council (NSERC)

National Science and Engineering Research Council (NSERC)

Canada Foundation for Innovation (CFI)

Canada Foundation for Innovation (CFI)

Canadian Diabetes Association

Canadian Diabetes Association

Brazilian Ministry of Education (CAPES)

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

CIHR Canadian Graduate Scholarship-Doctoral Award

CIHR Canadian Graduate Scholarship-Doctoral Award

Identificador

JOURNAL OF CELLULAR PHYSIOLOGY, v.217, n.2, p.478-485, 2008

0021-9541

http://producao.usp.br/handle/BDPI/27930

10.1002/jcp.21520

http://dx.doi.org/10.1002/jcp.21520

Idioma(s)

eng

Publicador

WILEY-LISS

Relação

Journal of Cellular Physiology

Direitos

restrictedAccess

Copyright WILEY-LISS

Palavras-Chave #MALONYL-COA DECARBOXYLASE #INDUCED INSULIN-RESISTANCE #GLUCOSE-METABOLISM #INHIBITION #CARNITINE #TISSUES #CYCLE #Cell Biology #Physiology
Tipo

article

original article

publishedVersion