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  • 标题:Multiplicity of Cytochrome P-450 Species Involved in Theophylline Metabolism in Mouse Hepatic Microsomes
  • 本地全文:下载
  • 作者:Hiroki KONISHI ; Kunihiko MORITA ; Akira YAMAJI
  • 期刊名称:Biological and Pharmaceutical Bulletin
  • 印刷版ISSN:0918-6158
  • 电子版ISSN:1347-5215
  • 出版年度:1995
  • 卷号:18
  • 期号:4
  • 页码:576-580
  • DOI:10.1248/bpb.18.576
  • 出版社:The Pharmaceutical Society of Japan
  • 摘要:To ascertain the multiplicity of the cytochrome P-450 (P-450) species participating in the individual metabolic conversion of theophylline by 8-hydroxylation, 3-demethylation and 1-demethylation in mice, kinetics were studied under various conditions using untreated and inducer-treated mouse hepatic microsomes. Eadie-Hofstee plots of 1-demethylation in untreated microsomes exhibited a straight line, whereas those of 8-hydroxylation and 3-demethylation were curved lines. The biphasic kinetics indicated the contribution of two P-450 populations to the respective metabolic pathways ; one characterized by high affinity and low capacity, the other by low affinity and high capacity. The high affinity population was efficiently induced by β-naphthoflavone (β-NF), and was highly susceptible to inhibition by a specific CYP1A inhibitor. The low affinity population was sensitive to induction by phenobarbital (PB), and was markedly inhibited by preferential inhibitors for PB-inducible P-450 species. The present results indicated that two P-450 populations contributed to the theophylline metabolism in mouse hepatic microsomes, and that the high and low affinity populations corresponded, respectively, to CYP1A, and a PB-inducible P-450 species having a much higher capacity than CYP1A.
  • 关键词:theophylline metabolism;cytochrome P-450 species;theophylline 8-hydroxylation;theophylline demethylation;CYP1A;mouse hepatic microsome
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