Isoferulic acid attenuates methylglyoxal-induced apoptosis in INS-1 rat pancreatic ?-cell through mitochondrial survival pathways and increasing glyoxalase-1 activity - 04/04/18
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Highlights |
• | Isoferulic acid (IFA) pretreatment decreased MG-induced cell apoptosis. |
• | IFA pretreatment attenuated oxidative stress caused by MG. |
• | IFA pretreatment improved MG-induced impairment of GSIS. |
• | IFA pretreatment decreased upregulation of Ucp 2 mRNA expression. |
• | IFA pretreatment protected MG-induced loss of GLO1 activity. |
Abstract |
Methylglyoxal (MG) is a reactive precursor to advanced glycation end-products (AGEs), which exert deleterious effects on cells and tissues. MG also causes pancreatic β-cell dysfunction and apoptosis. Isoferulic acid (IFA), a naturally occurring cinnamic acid derivative, is considered to be an antiglycating agent. However, the effect of IFA on MG-induced pancreatic β-cell dysfunction remains unknown. The objective of this study was to determine the protective effect of IFA against MG-induced mitochrondrial dysfunction and apoptosis in INS-1 pancreatic β-cells. The results showed that pretreatment of INS-1 cells with 100 μM IFA for 48 h prevented MG-induced decrease in cell viability and impairment of glucose-stimulated insulin secretion (GSIS). In addition, 100 μM IFA pretreatment also decreased MG-induced generation of reactive oxygen species (ROS) and upregulation of mitochondrial uncoupling protein 2 (Ucp2) mRNA expression. Furthermore, IFA pretreatment reduced MG-induced increase in caspase-3 activity, suggesting a reduction of apoptotic cell death. IFA (50–100 μM) itself markedly increased the activity of glyoxalase 1 (GLO1), a major enzyme for the detoxification of MG. The results showed that 100 μM IFA protected MG-induced loss of GLO1 activity in INS-1 cells. These findings suggest that IFA pretreatment attentuates MG-induced dysfunction and apoptosis in INS-1 pancreatic β-cells through mitochondrial survival pathway and increasing GLO1 activity.
Le texte complet de cet article est disponible en PDF.Keywords : Isoferulic acid, Methylglyoxal, Pancreatic β-cells, Mitochondrial uncoupling protein 2, Glyoxalase-1
Plan
Vol 101
P. 777-785 - mai 2018 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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