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

Keane DC, Takahashi HK, Dhayal S, Morgan NG, Curi R, Newsholme P - Clin. Sci. (2011)

Bottom Line: 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.AA decreased the protein expression of iNOS (inducible NO synthase), the p65 subunit of NF-κB (nuclear factor κB) and the p47 subunit of NADPH oxidase in PA-treated cells.These findings indicate that AA has an important regulatory and protective β-cell action, which may be beneficial to function and survival in the 'lipotoxic' environment commonly associated with Type 2 diabetes mellitus.

View Article: PubMed Central - PubMed

Affiliation: UCD School of Biomolecular and Biomedical Science, UCD Conway Institute and UCD Institute of Sport and Health, UCD Dublin, Belfield, Dublin 4, Ireland.

ABSTRACT
Chronic exposure of pancreatic β-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 β-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 β-cell line BRIN-BD11 and demonstrate AA-dependent attenuation of PA effects. When added to β-cell incubations at 100 μM, 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 Δ3,5,Δ2,4-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-κB (nuclear factor κB) and the p47 subunit of NADPH oxidase in PA-treated cells. These findings indicate that AA has an important regulatory and protective β-cell action, which may be beneficial to function and survival in the 'lipotoxic' environment commonly associated with Type 2 diabetes mellitus.

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Effect of AA on acute (20 min) insulin secretionBRIN-BD11 β-cells were incubated in the absence (Ctrl) or presence of 100 μM AA for 24 h. Subsequently, an acute (20 min) determination of basal- (1.1 mM glucose; black bars) and nutrient- (16.7 mM glucose and 10 mM alanine; white bars) stimulated insulin secretion was made. Results are expressed as means±S.E.M., for six independent experiments. *P<0.05 compared with basal insulin secretion from control cells.
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Figure 2: Effect of AA on acute (20 min) insulin secretionBRIN-BD11 β-cells were incubated in the absence (Ctrl) or presence of 100 μM AA for 24 h. Subsequently, an acute (20 min) determination of basal- (1.1 mM glucose; black bars) and nutrient- (16.7 mM glucose and 10 mM alanine; white bars) stimulated insulin secretion was made. Results are expressed as means±S.E.M., for six independent experiments. *P<0.05 compared with basal insulin secretion from control cells.

Mentions: A significant increase in basal- (1.1 mM glucose), but not nutrient-, (16.7 mM glucose and 10 mM alanine) stimulated (20 min) insulin secretion (P<0.05) was observed following 24 h exposure to 100 μM AA, when compared with the vehicle control (Figure 2).


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

Keane DC, Takahashi HK, Dhayal S, Morgan NG, Curi R, Newsholme P - Clin. Sci. (2011)

Effect of AA on acute (20 min) insulin secretionBRIN-BD11 β-cells were incubated in the absence (Ctrl) or presence of 100 μM AA for 24 h. Subsequently, an acute (20 min) determination of basal- (1.1 mM glucose; black bars) and nutrient- (16.7 mM glucose and 10 mM alanine; white bars) stimulated insulin secretion was made. Results are expressed as means±S.E.M., for six independent experiments. *P<0.05 compared with basal insulin secretion from control cells.
© Copyright Policy - open-access
Related In: Results  -  Collection

License
Show All Figures
getmorefigures.php?uid=PMC2990202&req=5

Figure 2: Effect of AA on acute (20 min) insulin secretionBRIN-BD11 β-cells were incubated in the absence (Ctrl) or presence of 100 μM AA for 24 h. Subsequently, an acute (20 min) determination of basal- (1.1 mM glucose; black bars) and nutrient- (16.7 mM glucose and 10 mM alanine; white bars) stimulated insulin secretion was made. Results are expressed as means±S.E.M., for six independent experiments. *P<0.05 compared with basal insulin secretion from control cells.
Mentions: A significant increase in basal- (1.1 mM glucose), but not nutrient-, (16.7 mM glucose and 10 mM alanine) stimulated (20 min) insulin secretion (P<0.05) was observed following 24 h exposure to 100 μM AA, when compared with the vehicle control (Figure 2).

Bottom Line: 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.AA decreased the protein expression of iNOS (inducible NO synthase), the p65 subunit of NF-κB (nuclear factor κB) and the p47 subunit of NADPH oxidase in PA-treated cells.These findings indicate that AA has an important regulatory and protective β-cell action, which may be beneficial to function and survival in the 'lipotoxic' environment commonly associated with Type 2 diabetes mellitus.

View Article: PubMed Central - PubMed

Affiliation: UCD School of Biomolecular and Biomedical Science, UCD Conway Institute and UCD Institute of Sport and Health, UCD Dublin, Belfield, Dublin 4, Ireland.

ABSTRACT
Chronic exposure of pancreatic β-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 β-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 β-cell line BRIN-BD11 and demonstrate AA-dependent attenuation of PA effects. When added to β-cell incubations at 100 μM, 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 Δ3,5,Δ2,4-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-κB (nuclear factor κB) and the p47 subunit of NADPH oxidase in PA-treated cells. These findings indicate that AA has an important regulatory and protective β-cell action, which may be beneficial to function and survival in the 'lipotoxic' environment commonly associated with Type 2 diabetes mellitus.

Show MeSH
Related in: MedlinePlus