Fujimura H, Tsurumi K, Yanagihara M, Hiramatsu Y, Tamura Y, Shimizu Y, Hojo M, Yoshida Y, Serizawa I
Nihon Yakurigaku Zasshi. 1981 Oct;78(4):249-60.
The action of an anti-histaminic agent, Mequitazine (LM-209) on the central nervous system was investigated. We found that LM-209 did not affect the spontaneous and co-operative movement in mice, did not induce muscle relaxation, analgesic effects or anti-convulsant effect in micr or hypothermic effects in rats. The anti-oxotremorine effect of LM-209 in mice was about 10 times more potent than clemastine fumarate (CL) and the same as promethazine. The activity and duration of the action were also superior to diethazine and orphenadrine used as an anti-Parkinson drug. LM-209 prolonged by 50% the hypnotic time induced by hexobarbital at 50 mg/kg (p.o.) in mice, while CL prolonged 50 and 100% it at 25 and 50 mg/kg (p.o.) respectively. In the EEG of rabbits, LM-209 produced a resting pattern, inhibited the arousal responses and recruiting responses and the effect was the same as CL and less potent than promethazine. From these results, the activity of LM-209 on the central nervous system (except for the anti-oxotremorine effect) seems to be the same as or somewhat less potent than CL. Therefore LM-209 should be an effective and anti-histaminic agent for clinical application.
对抗组胺药美喹他嗪(LM - 209)对中枢神经系统的作用进行了研究。我们发现,LM - 209不影响小鼠的自发和协同运动,不诱导小鼠肌肉松弛、镇痛作用或抗惊厥作用,也不引起大鼠体温过低。LM - 209对小鼠的抗氧化震颤素作用比富马酸氯马斯汀(CL)强约10倍,与异丙嗪相当。其活性和作用持续时间也优于用作抗帕金森病药物的二乙嗪和奥芬那君。在小鼠中,LM - 209使50 mg/kg(口服)己巴比妥诱导的催眠时间延长50%,而CL在25和50 mg/kg(口服)时分别使催眠时间延长50%和100%。在兔脑电图中,LM - 209产生静息模式,抑制觉醒反应和募集反应,其效果与CL相同,但比异丙嗪弱。从这些结果来看,LM - 209对中枢神经系统的作用(除抗氧化震颤素作用外)似乎与CL相同或略弱于CL。因此,LM - 209应是一种临床应用有效的抗组胺药。