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首页> 外文期刊>European journal of nutrition >Hepatic inflammation induced by high-fructose diet is associated with altered 11 beta HSD1 expression in the liver of Wistar rats
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Hepatic inflammation induced by high-fructose diet is associated with altered 11 beta HSD1 expression in the liver of Wistar rats

机译:高果糖饮食诱导的肝炎症与Wistar大鼠肝脏中11 beta HSD1表达的改变有关

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摘要

High fructose consumption provokes metabolic perturbations that result in chronic low-grade inflammation and insulin resistance. Glucocorticoids, potent anti-inflammatory hormones, have important role in pathogenesis of diet-induced metabolic disturbances. The aim of this study was to examine the link between glucocorticoid metabolism and inflammation in the liver of fructose-fed rats. Fructose-fed male Wistar rats consumed 60 % fructose solution for 9 weeks. Glucocorticoid prereceptor metabolism and signaling were analyzed by measuring the level of 11 beta-hydroxysteroid dehydrogenase type 1 (11 beta HSD1) and hexose-6-phosphate dehydrogenase expression, as well as via determination of intracellular corticosterone concentration, glucocorticoid receptor subcellular distribution and expression of its target gene, phosphoenolpyruvate carboxykinase. Nuclear factor kappa B (NF kappa B), tumor necrosis factor alpha (TNF alpha) and the level of inhibitory phosphorylation of insulin receptor substrate-1 (IRS-1) on Ser(307) were analyzed as markers of hepatic inflammation. The protein and/or mRNA levels of all examined molecules were assessed by Western blot and/or qPCR. Fructose-rich diet led to an enhancement of 11 beta HSD1 protein level in the liver, without affecting intracellular level of corticosterone and downstream glucocorticoid signaling. On the other hand, proinflammatory state was achieved through NF kappa B activation and increased TNF alpha expression, while elevated level of inhibitory phosphorylation of IRS-1 was observed as an early hallmark of insulin resistance. High-fructose diet does not influence hepatic glucocorticoid signaling downstream of the receptor, permitting development of NF kappa B-driven inflammation. The alteration in 11 beta HSD1 expression is most likely the consequence of enhanced inflammation, finally leading to disruption of insulin signaling in the rat liver
机译:高果糖摄入量会引起代谢紊乱,从而导致慢性低度炎症和胰岛素抵抗。糖皮质激素是有效的抗炎激素,在饮食引起的代谢紊乱的发病机理中具有重要作用。这项研究的目的是检查果糖喂养大鼠肝脏中糖皮质激素的代谢与炎症之间的联系。用果糖喂养的雄性Wistar大鼠消耗了60%果糖溶液达9周。通过测量11型β-羟类固醇脱氢酶1(11 beta HSD1)和己糖6-磷酸脱氢酶的表达水平,并通过测定细胞内皮质酮浓度,糖皮质激素受体亚细胞分布和表达来分析糖皮质激素受体的代谢和信号转导。其靶基因磷酸烯醇丙酮酸羧激酶。分析了Ser(307)上的核因子κB(NF kappa B),肿瘤坏死因子α(TNF alpha)和胰岛素受体底物1(IRS-1)的抑制磷酸化水平,作为肝炎的标志物。通过Western印迹和/或qPCR评估所有检查分子的蛋白质和/或mRNA水平。富含果糖的饮食可提高肝脏中11βHSD1蛋白的水平,而不会影响皮质酮的细胞内水平和下游糖皮质激素的信号传导。另一方面,通过NFκB活化和TNFα表达增加达到促炎状态,而观察到的IRS-1抑制性磷酸化水平升高是胰岛素抵抗的早期标志。高果糖饮食不影响受体下游的肝糖皮质激素信号传导,从而导致NFκB驱动的炎症的发展。 11 beta HSD1表达的改变很可能是炎症增强的结果,最终导致大鼠肝脏中胰岛素信号的破坏

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