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首页> 外文期刊>Chemico-biological interactions >Differential effect of valproate and its Delta2- and Delta4-unsaturated metabolites, on the beta-oxidation rate of long-chain and medium-chain fatty acids.
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Differential effect of valproate and its Delta2- and Delta4-unsaturated metabolites, on the beta-oxidation rate of long-chain and medium-chain fatty acids.

机译:丙戊酸酯及其Delta2和Delta4不饱和代谢物对长链和中链脂肪酸的β-氧化速率的差异作用。

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Overall fatty acid oxidation rates were investigated in rat hepatocytes using [9,10-3H]-palmitic, [9,10-3H]-oleic, [9,10-3H]-myristic and [2,3-3H]-phenylpropionic acids. The effect of both valproate (VPA) (0-10 mM) and two of its unsaturated metabolites, Delta2(E)-VPA and Delta4-VPA (0-10 mM), on the overall 3H2O production rate was studied. The results give evidence of a general inhibitory effect of VPA on the beta-oxidation rate of all the tested substrates. Similar effects were observed with both VPA metabolites but these effects appeared to be dependent on the chain length of the substrate. When the effect on the oxidation of the medium-chain fatty acid 3-phenylpropionate (PPA) was studied, Delta2(E)-VPA at 0.5 mM caused a 94% inhibition of the overall beta-oxidation rate. However, with long-chain substrates, 0.5 mM Delta(4)-VPA was a more potent inhibitor (20-30% of control activity) than 0.5 mM Delta(2E)-VPA (60-80% of control activity). Our results suggest that VPA and/or its metabolites inhibitfatty acyl-CoA metabolism within the mitochondrion by two different mechanisms. The first mechanism involves CoASH sequestration, which affects the oxidation rate of all fatty acids with different chain length. The second mechanism is more specific in nature and involves selective inhibition of particular enzymes implicated in fatty acid beta-oxidation.
机译:使用[9,10-3H]-棕榈酸,[9,10-3H]-油酸,[9,10-3H]-肉豆蔻酸和[2,3-3H]-苯基丙酸在大鼠肝细胞中研究了总脂肪酸氧化速率酸。研究了丙戊酸酯(VPA)(0-10 mM)及其两个不饱和代谢物Delta2(E)-VPA和Delta4-VPA(0-10 mM)对3H2O总体生产率的影响。结果提供了VPA对所有被测底物的β-氧化速率具有一般抑制作用的证据。两种VPA代谢物均观察到相似的作用,但这些作用似乎取决于底物的链长。当研究了对中链脂肪酸3-苯基丙酸酯(PPA)氧化的影响时,0.5 mM的Delta2(E)-VPA对总β-氧化速率产生94%的抑制作用。但是,对于长链底物,与0.5 mM Delta(2E)-VPA(控制活性的60-80%)相比,0.5 mM Delta(4)-VPA是更有效的抑制剂(控制活性的20-30%)。我们的结果表明,VPA和/或其代谢产物通过两种不同的机制抑制线粒体内的脂肪酰基CoA代谢。第一种机制涉及CoASH螯合,这会影响具有不同链长的所有脂肪酸的氧化速率。第二种机制本质上更具特异性,涉及选择性抑制与脂肪酸β-氧化有关的特定酶。

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