Tosihihiro Okamoto1,*, Shinichi Yoshida1, Tadashi
Kobayashi1 and Susumu Okabe2
1Research Laboratories, Nippon Chemiphar Co., Ltd., 1-22 Hikokawato,
Misato, Saitama 341-0005, Japan
2Department of Applied Pharmacology, Kyoto Pharmaceutical University,
Kyoto 607-8414, Japan
*Corresponding author. FAX: +81-489-52-0743
E-mail: ncokamot@green.ocn.ne.jp
Abstract: The effects of coumarin derivatives, osthole, imperatorin,
Pd-Ia, Pd-II and Pd-III, on mice concanavalin A (Con A) (0.2 mg/mouse, i.v.)-induced
hepatitis were studied. At the dose of 200 mg/kg (i.p.), these coumarins
inhibited more than 90% of the Con A-induced elevation of plasma alanine
aminotransferase activity, but glycyrrhizin (200 mg/kg, i.p.) caused only
45% inhibition. At the dose of 100 mg/kg (i.p.), osthole produced the strongest
inhibition among these coumarins. The inhibitory activity of osthole is
lost when its 7-methoxy group is replaced by a 7-hydroxy group to form osthenol.
The present results showed that coumarin derivatives inhibited Con A-induced
hepatitis, with osthole being the most inhibitory.
Keywords: Coumarin, Concanavalin A, Liver
Copyright The Japanese Pharmacological Society
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