Arachidonic acid actions on functional integrity and attenuation of the negative effects of palmitic acid in a clonal pancreatic beta-cell line


Autoria(s): KEANEI, Deirdre C.; TAKAHASHI, Hilton K.; DHAYAL, Shalinee; MORGAN, Noel G.; Curi, Rui; NEWSHOLME, Philip
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2011

Resumo

Chronic exposure of pancreatic beta-cells to saturated non-esterified fatty acids can lead to inhibition of insulin secretion and apoptosis. Several previous studies have demonstrated that saturated fatty acids such as PA (palmitic acid) are detrimental to beta-cell function compared with unsaturated fatty acids. In the present study, we describe the effect of the polyunsaturated AA (arachidonic acid) on the function of the clonal pancreatic beta-cell line BRIN-BD11 and demonstrate AA-dependent attenuation of PA effects. When added to beta-cell incubations at 100 mu M, AA can stimulate cell proliferation and chronic (24 h) basal insulin secretion. Microarray analysis and/or real-time PCR indicated significant AA-dependent up-regulation of genes involved in proliferation and fatty acid metabolism [e.g. Angptl (angiopoietin-like protein 4), Ech1 (peroxisomal Delta(3.5),Delta(2.4)-dienoyl-CoA isomerase), Cox-1 (cyclo-oxygenase-1) and Cox-2, P < 0.05]. Experiments using specific COX and LOX (lipoxygenase) inhibitors demonstrated the importance of COX-1 activity for acute (20 min) stimulation of insulin secretion, suggesting that AA metabolites may be responsible for the insulinotropic effects. Moreover, concomitant incubation of AA with PA dose-dependently attenuated the detrimental effects of the saturated fatty acid, so reducing apoptosis and decreasing parameters of oxidative stress [ROS (reactive oxygen species) and NO levels] while improving the GSH/GSSG ratio. AA decreased the protein expression of iNOS (inducible NO synthase), the p65 subunit of NF-kappa B (nuclear factor kappa B) and the p47 subunit of NADPH oxidase in PA-treated cells. These findings indicate that AA has an important regulatory and protective beta-cell action, which may be beneficial to function and survival in the `lipotoxic` environment commonly associated with Type 2 diabetes mellitus.

Health Research Board of Ireland[RP/2002/184]

Health Research Board of Ireland

European Foundation for Study of Diabetes

European Foundation for Study of Diabetes

Diabetes Research and Wellness Foundation (U.K.)

Diabetes Research and Wellness Foundation (U.K.)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq), Brazil

Identificador

CLINICAL SCIENCE, v.120, n.5/Jun, p.195-206, 2011

0143-5221

http://producao.usp.br/handle/BDPI/27983

10.1042/CS20100282

http://dx.doi.org/10.1042/CS20100282

Idioma(s)

eng

Publicador

PORTLAND PRESS LTD

Relação

Clinical Science

Direitos

restrictedAccess

Copyright PORTLAND PRESS LTD

Palavras-Chave #arachidonic acid #lipotoxicity #palmitic acid #pancreatic beta-cell #reactive oxygen species #Type 2 diabetes mellitus #FREE FATTY-ACIDS #ENDOPLASMIC-RETICULUM STRESS #INDUCED INSULIN-SECRETION #NITRIC-OXIDE #DIABETES-MELLITUS #GLUCOSE TOXICITY #OXIDATIVE STRESS #CHAIN-LENGTH #RAT ISLETS #INHIBITION #Medicine, Research & Experimental
Tipo

article

original article

publishedVersion