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首页> 外文期刊>Molecular and Cellular Biochemistry: An International Journal for Chemical Biology >Protective effects of arachidonic acid against palmitic acid-mediated lipotoxicity in HIT-T15 cells.
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Protective effects of arachidonic acid against palmitic acid-mediated lipotoxicity in HIT-T15 cells.

机译:花生四烯酸对棕榈酸介导的HIT-T15细胞脂毒性的保护作用。

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摘要

Saturated fatty acids have been considered major contributing factors in type 2 diabetes, whereas unsaturated fatty acids have beneficial effects for preventing the development of diabetes. However, the effects of polyunsaturated fatty acids in pancreatic β cells have not been reported. Here, we examined the effects of arachidonic acid (AA) on palmitic acid (PA)-mediated lipotoxicity in clonal HIT-T15 pancreatic β cells. AA prevented the PA-induced lipotoxicity as indicated by cell viability, DNA fragmentation and mitochondrial membrane potential, whereas eicosatetraynoic acid (ETYA), a non-metabolizable AA, had little effect on PA-induced lipotoxicity. In parallel with its protective effects against PA-induced lipotoxicity, AA restored impaired insulin expression and secretion induced by PA. AA but not ETYA increased intracellular triglyceride (TG) in the presence of PA compared with PA alone, and xanthohumol, a diacylglycerol acyltransferase (DGAT) inhibitor, reversed AA-induced protection from PA. Taken together, our results suggest that AA protects against PA-induced lipotoxicity in clonal HIT-T15 pancreatic β cells, and the protective effects may be associated with TG accumulation, possibly through sequestration of lipotoxic PA into TG.
机译:饱和脂肪酸被认为是2型糖尿病的主要促成因素,而不饱和脂肪酸具有预防糖尿病发展的有益作用。然而,尚未报道多不饱和脂肪酸在胰腺β细胞中的作用。在这里,我们检查了花生四烯酸(AA)对棕榈酸(PA)介导的克隆HIT-T15胰腺β细胞中脂毒性的影响。如细胞活力,DNA片段化和线粒体膜电位所示,AA阻止了PA诱导的脂毒性,而不可代谢的AA二十碳四烯酸(ETYA)对PA诱导的脂毒性几乎没有影响。与抗PA诱导的脂毒性的保护作用同时,AA恢复了PA诱导的胰岛素表达和分泌受损。与单独使用PA相比,在存在PA的情况下,AA而不是ETYA会增加细胞内甘油三酸酯(TG),而黄腐酚,一种二酰基甘油酰基转移酶(DGAT)抑制剂,则逆转了AA诱导的对PA的保护作用。两者合计,我们的结果表明,AA可预防PA诱导的克隆HIT-T15胰腺β细胞的脂毒性,并且这种保护作用可能与TG积累有关,可能是通过将脂毒性PA螯合到TG中来实现的。

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