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首页> 外文期刊>Hormone and Metabolic Research >Increase of peroxisome proliferator-activated receptor δ (PPARδ) by digoxin to improve lipid metabolism in the heart of diabetic rats
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Increase of peroxisome proliferator-activated receptor δ (PPARδ) by digoxin to improve lipid metabolism in the heart of diabetic rats

机译:地高辛增加过氧化物酶体增殖物激活受体δ(PPARδ)以改善糖尿病大鼠心脏的脂质代谢

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Increase of peroxisome proliferator-activated receptor δ (PPARδ) expression by digoxin in the heart of diabetic rats has been documented. The present study investigated the mediation of PPARδ in lipid metabolism improved by digoxin in the heart of diabetic rats and in the hyperglycemia-treated cardiomyocytes using the primary cultured cardiomyocytes from neonatal rat. The lipid deposition within the heart section was assessed in diabetic rats by oil red O staining. The fatty acid oxidation genes in cardiomyocytes were also examined. Inhibitor of calcium ions and siRNA-PPARδ were employed to investigate the potential mechanisms. After a 20-day digoxin treatment, the PPARδ expression was elevated in hearts of diabetic rats while the cardiac lipid deposition was reduced. In neonatal cardiomyocytes, digoxin also caused an increase in expressions of PPARδ and fatty acid oxidation genes. But both actions of digoxin were blocked by BAPTA-AM to chelate calcium ions and by siRNA-PPARδ in cardiomyocytes. The obtained results show that increase of PPARδ by digoxin is related to regulation of fatty acid oxidation genes in cardiac cells mediated by calcium-triggered signals.
机译:地高辛在糖尿病大鼠心脏中增加了过氧化物酶体增殖物激活的受体δ(PPARδ)表达。本研究调查了地高辛对糖尿病大鼠心脏和高血糖治疗的心肌细胞中PPARδ在脂质代谢中的介导作用,并使用了新生大鼠的原代培养心肌细胞。通过油红O染色评估糖尿病大鼠心脏部分内的脂质沉积。还检查了心肌细胞中的脂肪酸氧化基因。使用钙离子抑制剂和siRNA-PPARδ来研究其潜在机制。地高辛治疗20天后,糖尿病大鼠心脏PPARδ表达升高,而心脏脂质沉积减少。在新生儿心肌细胞中,地高辛还引起PPARδ和脂肪酸氧化基因表达的增加。但是地高辛的两种作用都被BAPTA-AM螯合钙离子和siRNA-PPARδ阻断了。获得的结果表明,地高辛增加PPARδ与钙触发信号介导的心肌细胞脂肪酸氧化基因的调节有关。

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