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
Metformin plus low-dose glimeperide significantly improves Homeostasis Model Assessment for insulin resistance (HOMA(IR)) and beta-cell function (HOMA(beta-cell)) without hyperinsulinemia in patients with type 2 diabetes mellitus.
Valmore Bermúdez-Pirela,Clímaco Cano,M. Medina,Aida Souki,Miguel A Lemus,Elliuz Leal,Hamid Seyfi,Raquel Cano,Ana Ciscek,Fernando Bermúdez-Arias,Freddy Contreras,Zafar H Israili,Rafael Hernández-Hernández,Manuel Valasco +13 more
TL;DR: Determination of HOMAIR and HOMAβ-cell values is an inexpensive, reliable, less invasive, and less labor-intensive method than other tests to estimate insulin resistance and β-cell function in patients with type 2 diabetes mellitus.
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Palmitate induces apoptosis in Schwann cells via both ceramide-dependent and independent pathways.
J. Suzuki,K. Akahane,Jiro Nakamura,Keiko Naruse,Hideki Kamiya,Tatsuhito Himeno,Nobuhisa Nakamura,Taiga Shibata,Masaki Kondo,Hiroshi Nagasaki,Atsushi Fujiya,Yutaka Oiso,Yoji Hamada +12 more
TL;DR: It is concluded that palmitate induces apoptosis in Schwann cells via both a ceramide-mediated, caspase-3-independent pathway and ceramicamide-independent, cospase- 3-dependent pathways.
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Oleic acid protects insulin-secreting INS-1E cells against palmitic acid-induced lipotoxicity along with an amelioration of ER stress.
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TL;DR: OA alleviated PA-induced lipotoxicity in INS-1E cells and improved insulin sensitivity in HFD rats and regulated the ER Ca2+ homeostasis, which may be responsible for its beneficial effects in β cells.
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The TLR4-IRE1α pathway activation contributes to palmitate-elicited lipotoxicity in hepatocytes
Chen Shen,Wang Ma,Lei Ding,Songtao Li,Xiaobing Dou,Zhenyuan Song,Zhenyuan Song,Zhenyuan Song +7 more
TL;DR: The findings suggest that targeting TLR4‐IRE1α pathway can be a potential therapeutic choice for the treatment of NAFLD as well as other metabolic disorders, with lipotoxicity being the principal pathomechanism.
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