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首页> 外文期刊>The 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
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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基因表达的改变,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

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pWe previously showed that the oxidation of branched-chain amino acids is increased in rats treated with clofibrate [Paul and Adibi (1980) J. Clin. Invest. b65/b, 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 Esub1/subα, Esub1/subβ, and Esub2/sub 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./p
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。Chem.Soc.Sci。,2001,9,1596-1,1992]。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,氯贝贝治疗对BCKDH的E 1 α,E 1 β和E 2 亚基的质量或丰度没有明显影响。编码这些亚基的mRNA。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。

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