首页> 美国卫生研究院文献>Nutrients >Effect of Cudrania tricuspidata and Kaempferol in Endoplasmic Reticulum Stress-Induced Inflammation and Hepatic Insulin Resistance in HepG2 Cells
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Effect of Cudrania tricuspidata and Kaempferol in Endoplasmic Reticulum Stress-Induced Inflammation and Hepatic Insulin Resistance in HepG2 Cells

机译:dra木和山emp酚对内质网应激诱导的HepG2细胞炎症和肝胰岛素抵抗的影响

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摘要

In this study, we quantitated kaempferol in water extract from Cudrania tricuspidata leaves (CTL) and investigated its effects on endoplasmic reticulum (ER) stress-induced inflammation and insulin resistance in HepG2 cells. The concentration of kaempferol in the CTL was 5.07 ± 0.08 mg/g. The HepG2 cells were treated with 300 µg/mL of CTL, 500 µg/mL of CTL, 1.5 µg/mL of kaempferol or 2.5 µg/mL of kaempferol, followed immediately by stimulation with 100 nM of thapsigargin for ER stress induction for 24 h. There was a marked increase in the activation of the ER stress and inflammation response in the thapsigargin-stimulated control group. The CTL treatment interrupted the ER stress response and ER stress-induced inflammation. Kaempferol partially inhibited the ER stress response and inflammation. There was a significant increase in serine phosphorylation of insulin receptor substrate (IRS)-1 and the expression of C/EBPα and gluconeogenic genes in the thapsigargin-stimulated control group compared to the normal control. Both CTL and kaempferol suppressed serine phosphorylation of IRS-1, and the treatments did not interrupt the C/EBPα/gluconeogenic gene pathway. These results suggest that kaempferol might be the active compound of CTL and that it might protect against ER stress-induced inflammation and hyperglycemia.
机译:在这项研究中,我们定量从虎杖叶片(CTL)的水提取物中定量山茱emp醇,并研究其对内质网(ER)应激诱导的HepG2细胞炎症和胰岛素抵抗的影响。 CTL中山奈酚的浓度为5.07±0.08 mg / g。用300 µg / mL的CTL,500 µg / mL的CTL,1.5 µg / mL的山emp酚或2.5 µg / mL的山emp酚处理HepG2细胞,然后立即用100 nM thapsigargin刺激以诱导ER应激24小时。在毒胡萝卜素刺激的对照组中,ER应激的激活和炎症反应明显增加。 CTL处理中断了ER应激反应和ER应激引起的炎症。山萘酚部分抑制内质网应激反应和炎症。与正常对照组相比,在毒胡萝卜素刺激的对照组中,胰岛素受体底物(IRS)-1的丝氨酸磷酸化以及C /EBPα和糖异生基因的表达显着增加。 CTL和山emp酚都抑制了IRS-1的丝氨酸磷酸化,并且这些处理均未中断C /EBPα/糖异生基因途径。这些结果表明,山fer酚可能是CTL的活性化合物,并且可以预防ER应激引起的炎症和高血糖。

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