首页> 外文期刊>Biopharmaceutics and Drug Disposition >Pharmacokinetics of intravenous chlorzoxazone in rats with dehydration and rehydration: effects of food intakes.
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Pharmacokinetics of intravenous chlorzoxazone in rats with dehydration and rehydration: effects of food intakes.

机译:脱水和补液大鼠静脉内氯唑沙宗的药代动力学:食物摄入量的影响。

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The following results were obtained recently from our laboratories; in rats with 72-h water deprivation (rats with dehydration), the hepatic cytochrome P450 2E1 (CYP2E1) was three-fold induced with an increase in the mRNA. Rehydration of 48-h water-deprived rats for the next 24 h with free access of food (rats with rehydration) restored CYP2E1 level to that of control. However, rehydration of 48-h water-deprived rats for the next 24 h with limited food supply (20% of control) failed to restore the CYP2E1 level to that of control. Hence, the CYP2E1 changes in rats with dehydration and rehydration resulted from differences in food intakes but not from dehydration or rehydration per'se. Chlorzoxazone (CZX) is metabolized to 6-hydroxychlorzoxazone (OH-CZX) mainly by CYP2E1 in rats. Therefore, the pharmacokinetics of CZX and OH-CZX were compared after intravenous administration of CZX, 25 mg/kg, to control rats and rats with dehydration and rehydration with free access of food. In rats with dehydration, theamount of 24-h urinary excretion of free OH-CZX plus its glucuronide conjugates (Ae (OH-CZX, 0-24 h,) expressed in terms of intravenous dose of CZX) was significantly greater (45.6 compared with 35.6%) and area under the plasma concentration-time curve from time zero to time infinity (AUC) of CZX was significantly smaller (2190 compared with 3200 micro g min/ml) than those in control rats. The above data indicated that the formation of OH-CZX increased significantly in rats with dehydration due to 3-fold induction of CYP2E1. In rats with rehydration with free access of food, the Ae (OH-CZX, 0-24 h) (39.0 compared with 35.6%) and AUC of CZX (2870 compared with 3200 micro g min/ml) were restored (comparable) to control levels since the expression of CYP2E1 in rats with dehydration returned to control level by rehydration. The above data indicate that CZX could be used as a chemical probe to assess the activity of CYP2E1 in rats with dehydration and rehydration. Copyright 2003 John Wiley & Sons, Ltd.
机译:最近从我们的实验室获得了以下结果;在缺水72小时的大鼠(有脱水的大鼠)中,肝细胞色素P450 2E1(CYP2E1)被诱导了三倍的mRNA表达增加。在接下来的24小时内,自由进食的48 h缺水大鼠(补充水分的大鼠)补液可将CYP2E1水平恢复至对照水平。然而,在食物供应有限(对照组的20%)的情况下,在接下来的24小时内,补水48小时的大鼠的补液未能使CYP2E1水平恢复至对照水平。因此,CYP2E1在具有脱水和补液作用的大鼠中的变化是由于食物摄入量的差异引起的,而不是由脱水或补液本身引起的。氯唑沙宗(CZX)主要通过CYP2E1在大鼠中代谢为6-羟基氯唑沙宗(OH-CZX)。因此,比较了静脉注射25 mg / kg的CZX来控制大鼠和具有脱水和补液作用且可自由进食的大鼠后CZX和OH-CZX的药代动力学。在脱水大鼠中,游离OH-CZX加上其葡糖苷酸结合物(Ae(OH-CZX,0-24 h,)以CZX静脉内剂量表示)的24小时尿排泄量显着增加(45.6与CZX的从零时到无限时(AUC)的血浆浓度-时间曲线下面积为35.6%,比对照大鼠要小得多(2190,而3200 micro g min / ml)。上述数据表明,由于CYP2E1的3倍诱导,脱水大鼠中OH-CZX的形成显着增加。在可自由进食的补液大鼠中,Ae(OH-CZX,0-24 h)(39.0比35.6%)和CZX的AUC(2870与3200 micro g min / ml比较)恢复到由于CYP2E1在脱水大鼠中的表达通过补液恢复到对照水平,因此控制水平。上述数据表明,CZX可用作化学探针,以评估脱水和补液大鼠中CYP2E1的活性。版权所有2003 John Wiley&Sons,Ltd.

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