Monounsaturated Fatty Acids Prevent the Deleterious Effects of Palmitate and High Glucose on Human Pancreatic β-Cell Turnover and Function
TL;DR: In human islets, the saturated palmitic acid and elevated glucose concentration induce beta-cell apoptosis, decreasebeta-cell proliferation, and impair beta- cell function, which can be prevented by monounsaturated fatty acids.
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Abstract: Glucotoxicity and lipotoxicity contribute to the impaired β-cell function observed in type 2 diabetes. Here we examine the effect of saturated and monounsaturated fatty acids at different glucose concentrations on human β-cell turnover and secretory function. Exposure of cultured human islets to saturated fatty acid and/or to an elevated glucose concentration for 4 days increased β-cell DNA fragmentation and decreased β-cell proliferation. In contrast, the monounsaturated palmitoleic acid or oleic acid did not affect DNA fragmentation and induced β-cell proliferation. Moreover, each monounsaturated fatty acid prevented the deleterious effects of both palmitic acid and high glucose concentration. The cell-permeable ceramide analogue C 2 -ceramide mimicked both the palmitic acid-induced β-cell apoptosis and decrease in proliferation. Furthermore, the ceramide synthetase inhibitor fumonisin B1 blocked the deleterious effects of palmitic acid on β-cell turnover. In addition, palmitic acid decreased Bcl-2 expression and induced release of cytochrome c from the mitochondria into the cytosol, which was prevented by fumonisin B1 and by oleic acid. Finally, each monounsaturated fatty acid improved β-cell secretory function that was reduced by palmitic acid and by high glucose. Thus, in human islets, the saturated palmitic acid and elevated glucose concentration induce β-cell apoptosis, decrease β-cell proliferation, and impair β-cell function, which can be prevented by monounsaturated fatty acids. The deleterious effect of palmitic acid is mediated via formation of ceramide and activation of the apoptotic mitochondrial pathway, whereas Bcl-2 may contribute to the protective effect of monounsaturated fatty acids.
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Citations
Novel Proapoptotic Effect of Hepatocyte Growth Factor: Synergy with Palmitate to Cause Pancreatic β-Cell Apoptosis
Jose A. Gonzalez-Pertusa,John J. Dubé,Shelley R. Valle,Taylor C. Rosa,Karen K. Takane,José Manuel Mellado-Gil,Germán Perdomo,Rupangi C. Vasavada,Adolfo Garcia-Ocaña +8 more
TL;DR: HGF can be detrimental for beta-cell survival in an environment with excessive fatty acid supply, and treatment of both mouse and human islet cells with the de novo ceramide synthesis inhibitors myriocin and fumonisin B1 abrogates beta- cell apoptosis induced by HGF and palmitate.
Protein kinase C delta (PKCδ) affects proliferation of insulin-secreting cells by promoting nuclear extrusion of the cell cycle inhibitor p21Cip1/WAF1.
Felicia Ranta,Johannes Leveringhaus,Dorothea Theilig,Gabriele Schulz-Raffelt,Anita M. Hennige,Dominic G. Hildebrand,René Handrick,Verena Jendrossek,Fatima Bosch,Klaus Schulze-Osthoff,Hans-Ulrich Häring,Susanne Ullrich +11 more
TL;DR: Observations disclose PKCδ as negative regulator of p21Cip1/WAF1, which facilitates proliferation of insulin secreting cells under stress-free conditions and suggest that additional stress-induced changes push PKC δ into its known pro-apoptotic role.
Palmitate induces DNA damage and senescence in human adipocytes in vitro that can be alleviated by oleic acid but not inorganic nitrate
TL;DR: In this article , the effects of palmitic acid (PA) on human subcutaneous and omental adipocytes were investigated in vitro, showing that PA induced DNA damage and increased p16INK4a levels.
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Sequential activation of caspases and synergistic β-cell cytotoxicity by palmitate and anti-Fas antibodies
TL;DR: Observations suggest that palmitate induces sequential activation of caspase-6 and caspased-3 through a mitochondrial signal(s), and cospase- 6 plays a primary role in the mechanism.
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Suppression of Peroxisome Proliferator-Activated Receptor γ-Coactivator-1α Normalizes the Glucolipotoxicity-Induced Decreased BETA2/NeuroD Gene Transcription and Improved Glucose Tolerance in Diabetic Rats
Ji-Won Kim,Young-Hye You,Dong-Sik Ham,Jae Hyoung Cho,Seung Hyun Ko,Ki-Ho Song,Ho-Young Son,Haeyoung Suh-Kim,Inkyu Lee,Kun-Ho Yoon +9 more
TL;DR: A better understanding of the functions of molecules such as PGC-1alpha, which play key roles in intracellular fuel regulation, could herald a new era of the treatment of patients with type 2 diabetes mellitus by providing protection from glucolipotoxicity, which is an important cause of the development and progression of the disease.
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