Sagara Y, Harano T, Omura T
J Biochem. 1978 Mar;83(3):807-12. doi: 10.1093/oxfordjournals.jbchem.a131976.
Nuclei and microsomes were prepared from the livers of normal, phenobarbital (PB)-treated and beta-naphthoflavone (beta-NF)-treated rats, and the contents of several enzymes in both subcellular fractions were examined. In normal rats, the enzyme activities in the nuclear fraction were about one-third of those of microsomes on a phospholipid basis. The induction of some particular enzymes by the drugs was observed with nuclei as well as with microsomes. Cytochrome P-450 and NADPH-cytochrome c reductase were increased by PB treatment and cytochrome P-448 was induced by beta-NF treatment both in nuclei and in microsomes. The extents of inhibition of nuclear enzyme activities by the antibodies against corresponding microsomal enzymes were almost the same as those of the microsomal activities. It was concluded that a microsomal type electron transport system exists in rat liver nuclei, and that nuclear drug-oxidizing activities are inducible by PB or beta-NF as their microsomal counterparts are.
从正常大鼠、经苯巴比妥(PB)处理的大鼠和经β-萘黄酮(β-NF)处理的大鼠肝脏中制备细胞核和微粒体,并检测这两种亚细胞组分中几种酶的含量。在正常大鼠中,以磷脂为基础,细胞核组分中的酶活性约为微粒体的三分之一。在细胞核以及微粒体中均观察到药物对某些特定酶的诱导作用。经PB处理后,细胞核和微粒体中的细胞色素P-450和NADPH-细胞色素c还原酶均增加;经β-NF处理后,细胞核和微粒体中的细胞色素P-448均被诱导。针对相应微粒体酶的抗体对细胞核酶活性的抑制程度与对微粒体活性的抑制程度几乎相同。得出的结论是,大鼠肝脏细胞核中存在微粒体类型的电子传递系统,并且细胞核中的药物氧化活性可像微粒体中的对应活性一样被PB或β-NF诱导。