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Circadian rhythm of cytochrome P4502E1 and its effect on disposition kinetics of chlorzoxazone in rats.

Circadian rhythm of cytochrome P4502E1 and its effect on disposition kinetics of chlorzoxazone in rats. Research Abstract Details 

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  • Circadian rhythm of cytochrome P4502E1 and its effect on disposition kinetics of chlorzoxazone in rats. Abstract Text:

    phisit khemawootPhisit Khemawoot,kousuke nishinoKousuke Nishino,junko ishizakiJunko Ishizaki,koichi yokogawaKoichi Yokogawa,ken-ichi miyamotoKen-ichi Miyamoto,phisit khemawootPhisit Khemawoot,kousuke nishinoKousuke Nishino,junko ishizakiJunko Ishizaki,koichi yokogawaKoichi Yokogawa,ken-ichi miyamotoKen-ichi Miyamoto,phisit khemawootPhisit Khemawoot,kousuke nishinoKousuke Nishino,junko ishizakiJunko Ishizaki,koichi yokogawaKoichi Yokogawa,ken-ichi miyamotoKen-ichi Miyamoto,

    The aim of this report is to study the circadian rhythm of cytochrome P4502E1 (CYP2E1) and its effect on the disposition kinetics of chlorzoxazone in male Wistar rats. The rats were housed under a 12-h light/dark cycle (lights from 9:00 to 21:00) with food and water ad libitum for 3 months. It was found that the expression of microsomal CYP2E1 mRNA in the liver during the dark phase was significantly lower than during the light phase, whereas the content of CYP2E1 protein and its hydroxylation activity were significantly higher. Therefore, chlorzoxazone 20 mg/kg was intravenously administered at 12:00 (light phase group) or 24:00 (dark phase group) to determine the effect on the disposition kinetics. The value of the area under the plasma concentration-time curve from 0 to 8 h (AUC(0-8 h)) of chlorzoxazone showed no significant difference between the two groups. However, the value of chlorzoxazone half-life in plasma of the light phase group was significant longer than the dark phase group. The AUC(0-8 h) of 6-hydroxychlorzoxazone, a metabolite formed from chlorzoxazone mainly by CYP2E1, was significantly higher in the dark phase than in the light phase. In conclusion, microsomal CYP2E1 shows a substantial circadian variation in rats, and this was associated with a decrease of chlorzoxazone half life, and an increase of 6-hydroxychlorzoxazone production. Therefore, the temporal variations of therapeutic response and toxicological effects may have to be taken into consideration for other xenobiotics that are predominantly metabolized by CYP2E1, particularly those with a short half-life.

    Circadian rhythm of cytochrome P4502E1 and its effect on disposition kinetics of chlorzoxazone in rats. Publishing Authors By Initials

    p khemawootP Khemawoot,k nishinoK Nishino,j ishizakiJ Ishizaki,k yokogawaK Yokogawa,k miyamotoK Miyamoto,p khemawootP Khemawoot,k nishinoK Nishino,j ishizakiJ Ishizaki,k yokogawaK Yokogawa,k miyamotoK Miyamoto,p khemawootP Khemawoot,k nishinoK Nishino,j ishizakiJ Ishizaki,k yokogawaK Yokogawa,k miyamotoK Miyamoto,

    For similar abstracts research abstracts see: abstracts research

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    Circadian rhythm of cytochrome P4502E1 and its effect on disposition kinetics of chlorzoxazone in rats. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: European journal of pharmacology

    VOLUME: 574

    Page Numbers: 71-6

    Journal Abbreviation: Eur. J. Pharmacol.

    ISSN: 0014-2999

    DAY: 29

    MONTH: 06

    YEAR: 2007

    Circadian rhythm of cytochrome P4502E1 and its effect on disposition kinetics of chlorzoxazone in rats. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 1254354

    Circadian rhythm of cytochrome P4502E1 and its effect on disposition kinetics of chlorzoxazone in rats. Keywords Mesh Terms:

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    Grant and Affiliation Information for Circadian rhythm of cytochrome P4502E1 and its effect on disposition kinetics of chlorzoxazone in rats.

    AFFILIATION: Department of Medicinal Informatics, Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University, Japan.

    Country: Netherlands

    Netherlands Research PublicationNetherlands Research Publication

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    MEDLINETA: Eur J Pharmacol

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