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细胞色素P4504A1的共诱导与过氧化物酶体增殖:因果关系还是偶然关系?

Co-induction of cytochrome P4504A1 and peroxisome proliferation: a causal or casual relationship?

作者信息

Gibson G G

机构信息

University of Surrey, School of Biological Sciences, Molecular Toxicology Group, Guildford, UK.

出版信息

Xenobiotica. 1992 Sep-Oct;22(9-10):1101-9. doi: 10.3109/00498259209051864.

DOI:10.3109/00498259209051864
PMID:1441601
Abstract
  1. The hypothesis that xenobiotic induction of hepatic microsomal cytochrome P4504A1 and peroxisome proliferation are closely-related phenomena has been further investigated. 2. Five rat strains (Gunn, Fischer, Wistar, Long Evans and Sprague Dawley) were all susceptible to xenobiotic induction of both microsomal cytochrome P4504A1 and peroxisome proliferation, and no strain exhibited a dissociation of these phenomena. 3. In comparison to rat, the marmoset was substantially less susceptible to the above hepatic changes. 4. Induction of both cytochrome P4504A1 and peroxisome proliferation by a structural analogue of clofibrate (2-(4-(4-chlorophenyl)benzyloxy)-2-phenyl acetic acid) demonstrated stereochemical selectivity, in that the R(-)-isomer was a more potent inducer of both phenomena than the S(+)-antipode, with the racemic mixture exhibiting an intermediate potency. 5. Cycloheximide inhibition of clofibrate-dependent induction of acyl CoA mRNA, but not cytochrome P4504A1 mRNA has indicated a protein dependency for peroxisome proliferation, not inconsistent with participation of cytochrome P4504A1 in the biogenesis of peroxisome proliferation. 6. Taken collectively, the data described herein provide further evidence for a close linkage between xenobiotic induction of cytochrome P4504A1 and peroxisome proliferation, and possible molecular mechanisms inter-relating these two phenomena are discussed.
摘要
  1. 关于外源化学物诱导肝微粒体细胞色素P4504A1和过氧化物酶体增殖是密切相关现象的假说已得到进一步研究。2. 五种大鼠品系(冈恩、费希尔、Wistar、长 Evans 和斯普拉格·道利)对外源化学物诱导微粒体细胞色素P4504A1和过氧化物酶体增殖均敏感,没有品系表现出这些现象的分离。3. 与大鼠相比,狨猴对上述肝脏变化的敏感性要低得多。4. 氯贝丁酯的一种结构类似物(2-(4-(4-氯苯基)苄氧基)-2-苯基乙酸)对细胞色素P4504A1和过氧化物酶体增殖的诱导表现出立体化学选择性,即R(-)-异构体比S(+)-对映体对这两种现象的诱导作用更强,外消旋混合物表现出中等效力。5. 环己酰亚胺抑制氯贝丁酯依赖性酰基辅酶A mRNA的诱导,但不抑制细胞色素P4504A1 mRNA,这表明过氧化物酶体增殖存在蛋白质依赖性,这与细胞色素P4504A1参与过氧化物酶体增殖的生物发生并不矛盾。6. 总体而言,本文所述数据为细胞色素P4504A1的外源化学物诱导与过氧化物酶体增殖之间的紧密联系提供了进一步证据,并讨论了与这两种现象相关的可能分子机制。

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