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首页> 外文期刊>Biochemical and Biophysical Research Communications >Peroxisome proliferator-activated receptor a agonist-induced down-regulation of hepatic glucocorticoid receptor expression in SD rats
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Peroxisome proliferator-activated receptor a agonist-induced down-regulation of hepatic glucocorticoid receptor expression in SD rats

机译:过氧化物体增殖物激活受体A激动剂诱导的SD大鼠肝糖皮质激素受体表达的下调

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摘要

It was reported that glucocorticoid production was inhibited by fenofibrate through suppression of type-1 11 beta-hydroxysteroid dehydrogenase gene expression in liver. The inhibition might be a negative-feedback regulation of glucocorticoid receptor (GR) activity by peroxisome proliferator-activated receptor alpha (PPAR alpha), which is quickly induced by glucocorticoid in the liver. However, it is not clear if GR expression is changed by fenofibrate-induced PPAR alpha activation. In this study, we tested this possibility in the liver of Sprague-Dawley rats. GR expression was reduced by fenolibrate in a time- and does-dependent manner. The inhibition was observed in liver, but not in fat and muscle. The corticosterone level in the blood was increased significantly by fenofibrate. These effects of fenofibrate were abolished by PPAR alpha inhibitor MK886, suggesting that fenofibrate activated through PPAR alpha. In conclusion, inhibition of GR expression may represent a new molecular mechanism for the negative feedback regulation of GR activity by PPAR alpha. (C) 2008 Elsevier Inc. All rights reserved.
机译:据报道,通过抑制肝脏抑制111型β-羟类脱氢酶基因表达,通过糖纤维酸盐抑制糖皮质激素产生。抑制可能是过氧化物体增殖物激活的受体α(PPARα)的糖皮质激素受体(GR)活性的负反馈调节,其通过肝脏在肝脏中快速诱导。但是,如果通过面包纤维诱导的PPARα激活改变GR表达,则尚不清楚。在这项研究中,我们测试了Sprague-Dawley大鼠肝脏的这种可能性。芬尔纤板以时间和依赖性方式减少了GR表达。在肝脏中观察到抑制,但不含脂肪和肌肉。血纤维血液中皮质酮水平显着增加。通过PPARα抑制剂MK886废除了非芬纤维的这些效果,表明通过PPARα激活非芬纤维。总之,GR表达的抑制可以代表PPARα的GR活性对GR活性的负反馈调节的新分子机制。 (c)2008年elestvier Inc.保留所有权利。

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