Jpn. J. Pharmacol. 75 (3), 283-290 (1997)


Chronotoxicity of Methotrexate in Mice and Its Relation to Circadian Rhythm of DNA Synthesis and Pharmacokinetics

Shigehiro Ohdo (1), Kouichi Inoue (1), Eiji Yukawa (1), Shun Higuchi (1), Shigeyuki Nakano (2) and Nobuya Ogawa (3)


(1) Department of Clinical Pharmacokinetics, Division of Pharmaceutical Science, Kyushu University, Fukuoka 812, Japan
(2) Department of Clinical Pharmacology and Therapeutics, Oita Medical University, Oita 879-55, Japan
(3) Department of Pharmacology, Ehime University School of Medicine, Ehime 791-02, Japan

Abstract: The mechanisms underlying the circadian rhythm of methotrexate (MTX-induced toxicity (body weight loss and leukopenia) were investigated from the viewpoints of the sensitivity of living organisms to the drug and the pharmacokinetics of the drug. ICR male mice were housed in a standardized light-dark cycle (lights on at 0700, off at 1900) with food and water ad libitum. The body weight loss after an intraperitoneal injection of MTX (400 mg/kg) was more serious in the late dark period and the early light period and milder in the late light period and the early dark period. The MTX-induced leukopenia was more serious in the late dark period and the light period and milder in the early dark period. Lower toxicity was observed when DNA synthesis, dihydrofolate reductase (DHFR) activity in bone marrow cells and folate level in plasma decreased, and higher toxicity was observed when they increased. There was a significant circadian rhythm in plasma MTX concentration, with a higher level in the light period and a lower level in the dark period. The circadian rhythm of plasma MTX concentration was associated with that of MTX-induced toxicity. The present study suggests that the circadian rhythm of MTX-induced toxicity is caused by that of the sensitivity of living organisms to the drug and the pharmacokinetics of the drug.

Keywords: Methotrexate, Chronotoxicity, Chronopharmacokinetics, Cell cycle, Circadian rhythm


Copyrightę The Japanese Pharmacological Society 1997

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