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甲氨蝶呤在小鼠中的时辰毒性和时辰药代动力学:进食时间表的影响

Chronotoxicity and chronopharmacokinetics of methotrexate in mice: modification by feeding schedule.

作者信息

Song J G, Nakano S, Ohdo S, Ogawa N

机构信息

Department of Pharmacology, Ehime University School of Medicine, Japan.

出版信息

Jpn J Pharmacol. 1993 Aug;62(4):373-8. doi: 10.1254/jjp.62.373.

Abstract

The circadian rhythms of the toxicity and the pharmacokinetics of methotrexate (MTX), as well as the effects of manipulation of feeding schedule on the rhythms, were investigated in mice. Male ICR mice were housed under a standardized light-dark cycle (12:12) with food and water ad libitum (ALF) or under the time-restricted feeding (TRF) schedule (8 hr during the light phase) for 1 day or 14 days before the drug administration. The animals received MTX (100 mg/kg, i.p.) once daily for 7 days in the toxicity studies and a single dose of MTX (100 mg/kg, i.p.) for the kinetic studies. Under the ALF, a significant dosing time dependency was demonstrated for the toxicity of MTX with a longer survival time for the middark dosing and a shorter one for the midlight dosing. The MTX kinetics also showed a significant rhythm, with the highest clearance at middark and the lowest one at midlight. The rhythm in MTX kinetics well coincided with that in the toxicity of the drug. The TRF had a marked influence on the rhythms of MTX kinetics and toxicity. Thus, the timing of dosing is important in the kinetics and the toxicity of MTX in mice, and the manipulation of feeding schedule can modify the rhythm of the toxicity by changing that of the MTX kinetics.

摘要

在小鼠中研究了甲氨蝶呤(MTX)的毒性和药代动力学的昼夜节律,以及进食时间安排的改变对这些节律的影响。雄性ICR小鼠在给药前1天或14天,饲养于标准化的明暗循环(12:12)下,自由摄食和饮水(ALF),或采用限时进食(TRF)方案(光照期8小时)。在毒性研究中,动物每天腹腔注射MTX(100mg/kg),连续7天;在药代动力学研究中,动物单次腹腔注射MTX(100mg/kg)。在ALF条件下,MTX的毒性表现出明显的给药时间依赖性,午夜给药存活时间较长,中午给药存活时间较短。MTX的药代动力学也呈现出显著的节律性,午夜清除率最高,中午最低。MTX药代动力学的节律与药物毒性的节律非常吻合。TRF对MTX药代动力学和毒性的节律有显著影响。因此,给药时间对小鼠MTX的药代动力学和毒性很重要,改变进食时间安排可以通过改变MTX药代动力学的节律来改变毒性节律。

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