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首页> 外文期刊>The biochemical journal >Comparison of the activities of some peroxisomal and extraperoxisomal lipid-metabolizing enzymes in liver and extrahepatic tissues of the rat
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Comparison of the activities of some peroxisomal and extraperoxisomal lipid-metabolizing enzymes in liver and extrahepatic tissues of the rat

机译:肝脏肝脏肝外组织中一些过氧甲基酶体和题象素脂质代谢酶活性的比较

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pPeroxisomal (acyl-CoA oxidase and peroxisomal dihydroxyacetone-phosphate acyltransferase) and extraperoxisomal (mitochondrial fatty acid oxidation, extraperoxisomal dihydroxyacetone-phosphate acyltransferase, mitochondrial and microsomal glycerophosphate acyltransferases) lipid-metabolizing enzymes were measured in homogenates from rat liver and from seven extrahepatic tissues. Except for jejunal mucosa and kidney, extrahepatic tissues contained very little acyl-CoA oxidase activity. Peroxisomal dihydroxyacetone-phosphate acyltransferase, taken as the activity that was not inhibited by 5 mM-glycerol 3-phosphate, was present in all tissues examined, and its specific activity in liver and extrahepatic tissues was roughly of the same order of magnitude. Clofibrate treatment increased the activity of acyl-CoA oxidase in liver, and to a smaller extent also in kidney, but did not influence the activity of peroxisomal dihydroxyacetone-phosphate acyltransferase. Comparison of the activities of peroxisomal and extraperoxisomal lipid-metabolizing enzymes in extrahepatic tissues and in liver, an organ in which the contribution of peroxisomes to fatty acid oxidation and to glycerolipid synthesis has been estimated previously, suggests that, as in liver, peroxisomal long-chain fatty acid oxidation is of minor quantitative importance in extrahepatic tissues, but that in these tissues (micro)-peroxisomes are responsible for most of the dihydroxyacetone phosphate acylation and, consequently, for initiating ether glycerolipid synthesis./p
机译:[p>过氧乙酰酶(酰基-CoA氧化酶和过氧磷酸异甲酸氨基丙酮酰酰基转移酶)和外体异素(线粒体脂肪酸氧化,左旋体异素二羟基丙酮 - 磷酸酰氯转移酶,线粒体和微粒体甘油磷酸酰酰基转移酶)在大鼠肝脏均质中测量脂质代谢酶,七分脱胸部组织。除Jejunal Mucosa和肾脏外,肝外组织含有非常小的酰基-CoA氧化酶活性。在所有检查的组织中存在过氧化异喹啉二羟基丙酮 - 磷酸酰基转移酶作为未被5mM-甘油3-磷酸盐抑制的活性,其在肝脏和嗜肠组织中的特异性活性大致是相同的数量级。 Clofibrate治疗增加了肝脏酰基-CoA氧化酶的活性,并且在肾脏中也较小程度,但没有影响过氧异甲基二羟基丙酮磷酸酰酰基转移酶的活性。过分血磷和外素脂质脂质代谢酶活性的比较初中组织和肝脏中的一种器官,其中过氧缺氧对脂肪酸氧化和甘油脂合成的贡献已经估计,表明,如肝脏,过氧硅片长 - 链脂肪酸氧化在脱胸部组织中具有轻微的定量重要性,但在这些组织(微)(微) - 氧血清素中对大多数二羟基丙酮磷酸酰化丙烯化负责,因此用于启动醚甘油脂合成。

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