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  • 标题:Effects of Dietary Pantethine Levels on Drug-Metabolizing System in the Liver of Rats Orally Administered Varying Amounts of Autoxidized Linoleate
  • 本地全文:下载
  • 作者:Naoko HIRAMATSU ; Tadaaki KISHIDA ; Masato NATAKE
  • 期刊名称:Journal of Nutritional Science and Vitaminology
  • 印刷版ISSN:0301-4800
  • 电子版ISSN:1881-7742
  • 出版年度:1989
  • 卷号:35
  • 期号:4
  • 页码:303-313
  • DOI:10.3177/jnsv.35.303
  • 出版社:Center for Academic Publications Japan
  • 摘要:The effects of dietary pantethine levels on the drugmetabolizing system were investigated under administration of varying amounts of autoxidized linoleate (AL) with rat liver microsomes and S-9 fractions. AL having 800meq/kg of peroxide value and 1, 700meq/kg of carbonyl value was dosed to the rats of each group given drinking water containing 0mg% (deficient), 6.25mg% (normal), and 125mg% pantethine (sufficient). The contents and activities of the enzymes in the drugmetabolizing system in the rat liver of each pantethine-level group changed essentially in a similar manner, that is, they were induced at an AL daily dose of 0.2ml/100g body weight ( i.e. , small dose) for 5 successive days and lowered at a daily dose of 0.4ml/100g body weight ( i.e. , large dose) by the same administration period, compared with respective nonAL groups in each of the three pantethine levels. In both non-AL and the small-dose AL, enzyme activities of the electron transfer system in rat liver microsomes, aminopyrin-N-demethylase activity, and metabolic activation of 2-acetylaminofluorene in S-9 fractions were significantly higher in the pantethine-deficient group than in the pantethine-normal and sufficient groups. In the large-dose AL, the enzyme activities in the drugmetabolizing system decreased significantly in any pantethine levels, though the survival rate of the rats was higher in the pantethine-sufficient group than in the pantethine-normal groups. The results suggest that the pantethine relieves the effect of dosed AL on the drug-metabolizing system in rat liver.
  • 关键词:autoxidized linoleic acid;microsome;cytochrome P-450;cytochrome b5;electron transfer system;drug-metabolizing activity;aminopyrin-N-demethylase;S-9 activity;pantethine
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