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首页> 外文期刊>Journal of Molecular Endocrinology >PPAR ligands improve impaired metabolic pathways in fetal hearts of diabetic rats
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PPAR ligands improve impaired metabolic pathways in fetal hearts of diabetic rats

机译:PPAR配体可改善糖尿病大鼠胎儿心脏中受损的代谢途径

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In maternal diabetes, the fetal heart can be structurally and functionally affected. Maternal diets enriched in certain unsaturated fatty acids can activate the nuclear receptors peroxisome proliferator-activated receptors (PPARs) and regulate metabolic and anti-inflammatory pathways during development. Our aim was to investigate whether PPARα expression, lipid metabolism, lipoperoxidation, and nitric oxide (NO) production are altered in the fetal hearts of diabetic rats, and to analyze the putative effects of in vivo PPAR activation on these parameters. We found decreased PPARα expression in the hearts of male but not female fetuses of diabetic rats when compared with controls. Fetal treatments with the PPARα ligand leukotriene B4 upregulated the expression of PPARα and target genes involved in fatty acid oxidation in the fetal hearts. Increased concentrations of triglycerides, cholesterol, and phospholipids were found in the hearts of fetuses of diabetic rats. Maternal treatments with diets supplemented with 6% olive oil or 6% safflower oil, enriched in unsaturated fatty acids that can activate PPARs, led to few changes in lipid concentrations, but up-regulated PPARα expression in fetal hearts. NO production, which was increased in the hearts of male and female fetuses in the diabetic group, and lipoperoxidation, which was increased in the hearts of male fetuses in the diabetic group, was reduced by the maternal treatments supplemented with safflower oil. In conclusion, impaired PPARα expression, altered lipid metabolism, and increased oxidative and nitridergic pathways were evidenced in hearts of fetuses of diabetic rats and were regulated in a gender-dependent manner by treatments enriched with PPAR ligands.
机译:在孕产妇糖尿病中,胎儿心脏会受到结构和功能的影响。富含某些不饱和脂肪酸的孕妇饮食可以激活核受体过氧化物酶体增殖物激活受体(PPAR),并在发育过程中调节代谢和抗炎途径。我们的目的是研究糖尿病大鼠胎儿心脏中PPARα的表达,脂质代谢,脂过氧化和一氧化氮(NO)的产生是否发生改变,并分析体内PPAR激活对这些参数的假定影响。我们发现,与对照组相比,糖尿病大鼠雄性而非雌性胎儿心脏中PPARα表达降低。用PPARα配体白三烯B4进行的胎儿治疗上调了胎儿心脏中PPARα和涉及脂肪酸氧化的靶基因的表达。在糖尿病大鼠的胎儿心脏中发现甘油三酯,胆固醇和磷脂的浓度增加。孕妇饮食中添加了6%橄榄油或6%红花油,富含不饱和脂肪酸,可以激活PPAR,导致血脂浓度变化很小,但在胎儿心脏中PPARα表达上调。补充红花油的孕产妇治疗减少了糖尿病组男女胎儿心脏中NO的产生,而糖尿病组男女胎儿心脏中脂质过氧化的增加。总之,在糖尿病大鼠的胎儿心脏中,PPARα表达受损,脂质代谢改变,氧化和硝化途径增加,并通过富含PPAR配体的治疗以性别依赖性方式受到调节。

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