首页> 美国卫生研究院文献>Biochemical Journal >Alteration in gene expression of branched-chain keto acid dehydrogenase kinase but not in gene expression of its substrate in the liver of clofibrate-treated rats.
【2h】

Alteration in gene expression of branched-chain keto acid dehydrogenase kinase but not in gene expression of its substrate in the liver of clofibrate-treated rats.

机译:支链酮酸脱氢酶激酶的基因表达改变,但在氯贝贝特治疗的大鼠肝脏中其底物的基因表达没有改变。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

We previously showed that the oxidation of branched-chain amino acids is increased in rats treated with clofibrate [Paul and Adibi (1980) J. Clin. Invest. 65, 1285-1293]. Two subsequent studies have reported contradictory results regarding the effect of clofibrate treatment on gene expression of branched-chain keto acid dehydrogenase (BCKDH) in rat liver. Furthermore, there has been no previous study of the effect of clofibrate treatment on gene expression of BCKDH kinase, which regulates the activity of BCKDH by phosphorylation. The purpose of the present study was to investigate the above issues. Clofibrate treatment for 2 weeks resulted in (a) a 3-fold increase in the flux through BCKDH in mitochondria isolated from rat liver, and (b) a modest but significant increase in the activity of BCKDH. However, clofibrate treatment had no significant effect on the mass of E1 alpha, E1 beta, and E2 subunits of BCKDH or the abundance of mRNAs encoding these subunits. On the other hand, clofibrate treatment significantly reduced the activity, the protein mass and the mRNA levels of BCKDH kinase in the liver. In contrast to the results obtained in liver, clofibrate treatment had no significant effect on any of these parameters of BCKDH kinase in the skeletal muscle. In conclusion, our results show that clofibrate treatment increases the activity of BCKDH in the liver and the mechanism of this effect is the inhibition of gene expression of the BCKDH kinase.
机译:我们先前表明,用氯贝贝特治疗的大鼠中支链氨基酸的氧化增加[Paul and Adibi(1980)J. Clin。Biol。投资。 65,1285-1293]。随后的两项研究报道了氯贝贝特治疗对大鼠肝脏支链酮酸脱氢酶(BCKDH)基因表达的影响的矛盾结果。此外,以前还没有关于氯贝特治疗对BCKDH激酶基因表达的影响的研究,该基因通过磷酸化调节BCKDH的活性。本研究的目的是调查上述问题。氯贝特治疗2周导致(a)从大鼠肝脏分离的线粒体中通过BCKDH的通量增加了3倍,并且(b)BCKDH活性适度但显着增加。但是,氯贝贝特治疗对BCKDH的E1 alpha,E1 beta和E2亚基的质量或编码这些亚基的mRNA的丰度没有显着影响。另一方面,氯贝贝特治疗显着降低了肝脏中BCKDH激酶的活性,蛋白质质量和mRNA水平。与在肝脏中获得的结果相反,氯贝贝特治疗对骨骼肌中BCKDH激酶的任何这些参数均无明显影响。总之,我们的结果表明,氯贝贝特治疗可增加肝脏中BCKDH的活性,其作用机制是抑制BCKDH激酶的基因表达。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号