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降血脂及致癌剂氯贝丁酯诱导的大鼠肝脏过氧化物酶体的多分散性。

Polydispersity of rat liver peroxisomes induced by the hypolipidemic and carcinogenic agent clofibrate.

作者信息

Flatmark T, Christiansen E N, Kryvi H

出版信息

Eur J Cell Biol. 1981 Apr;24(1):62-9.

PMID:7238535
Abstract
  1. The present study has confirmed that the hypolipidemic and carcinogenic agent clofibrate induces a marked increase in the specific activity of some peroxisomal marker enzymes in rat liver homogenates, notably of the palmitoyl-CoA dependent dehydrogenase and catalase activities. 2. Clofibrate was found to induce a marked polydispersity of the peroxisomes as determined by analytical differential centrifugation of homogenates and morphometric analysis of hepatocytes. 3. Two major populations of peroxisomes were detected by analytical differential centrifugation under conditions which reduce the hydrostatic pressure effects on the organelle to a minimum. Using urate oxidase as the marker enzyme, the S4,B-values of the two populations were estimated to 1 1 860 S and 4240 S, both different from that of the homogenous population of peroxisomes in the control animals (S4,B approximately equal to 6680 S). The 4240 S-population induced by clofibrate revealed a high specific activity relative to that of of urate oxidase and particularly relative to that of catalase, which was very low. In addition, a less distinct population of particles (870 S lees than S lees than 4240 S) contained more than 50% of the total particle-bound palmitoyl-CoA dependent dehydrogenase activity sedimented at a centrifugal effect of t integral of 0 rmp(2)dt = 1.5 x 10(10) min(-1), but not urate oxidase and catalase activities. This fraction was not observed in the homogenates of normal rats. As in the normal controls, the palmitoyl-CoA dependent dehydrogenase activity was found to be particle-bound (S greater than 870 S). 4. Morphometric analyses of randomly selected hepatocytes revealed that after clofibrate treatment the relative volume fraction of the peroxisomes increased by a factor of 5.5 and thier average diameter and volume by a factor of 1.3 and 2.1, respectively. Furthermore, the frequency of electron-dense matrix cores decreased on clofibrate treatment. In contrast, no change was observed in the average size of the mitochondria, and their relative volume fraction increased only by a factor of 1.2. 5. The clofibrate induced changes in eh morphological and biochemical properties of rat liver peroxisomes appears to be a very useful model system in which to study the biogenesis as well as the biochemical and physiological role(s) of this organelle in mammalian cells.
摘要
  1. 本研究证实,降血脂及致癌剂氯贝丁酯可使大鼠肝脏匀浆中某些过氧化物酶体标记酶的比活性显著增加,尤其是棕榈酰辅酶A依赖性脱氢酶和过氧化氢酶的活性。2. 通过对匀浆进行分析性差速离心及对肝细胞进行形态计量分析发现,氯贝丁酯可诱导过氧化物酶体出现明显的多分散性。3. 在将细胞器上的流体静压效应降至最低的条件下,通过分析性差速离心检测到了过氧化物酶体的两个主要群体。以尿酸氧化酶作为标记酶,估计这两个群体的S4,B值分别为11860 S和4240 S,均与对照动物过氧化物酶体的均匀群体(S4,B约等于6680 S)不同。氯贝丁酯诱导产生的4240 S群体相对于尿酸氧化酶,尤其是相对于过氧化氢酶,显示出较高的比活性,而过氧化氢酶的比活性非常低。此外,一个不太明显的颗粒群体(870 S<S<4240 S)含有超过50%的与颗粒结合的棕榈酰辅酶A依赖性脱氢酶活性,在离心力积分t∫0 rmp(2)dt = 1.5×10(10) min(-1)时沉淀,但不含有尿酸氧化酶和过氧化氢酶活性。在正常大鼠的匀浆中未观察到该部分。与正常对照一样,棕榈酰辅酶A依赖性脱氢酶活性被发现与颗粒结合(S>870 S)。4. 对随机选取的肝细胞进行形态计量分析显示,氯贝丁酯处理后,过氧化物酶体的相对体积分数增加了5.5倍,其平均直径和体积分别增加了1.3倍和2.1倍。此外,氯贝丁酯处理后电子致密基质核心的频率降低。相比之下,线粒体的平均大小未观察到变化,其相对体积分数仅增加了1.2倍。5. 氯贝丁酯诱导的大鼠肝脏过氧化物酶体形态和生化特性的变化似乎是一个非常有用的模型系统,可用于研究该细胞器在哺乳动物细胞中的生物发生以及生化和生理作用。

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Polydispersity of rat liver peroxisomes induced by the hypolipidemic and carcinogenic agent clofibrate.降血脂及致癌剂氯贝丁酯诱导的大鼠肝脏过氧化物酶体的多分散性。
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