Shizawa T, Ohmori S, Maeda K, Sakata K, Ishii T, Kamitani T
Research & Development Center, Terumo Corp., Kanagawa, Japan.
Arzneimittelforschung. 1996 Nov;46(11):1072-6.
The ability of linetastine (TMK688, 1-[¿5'-(3"-methoxy-4"-ethoxycarbonyloxyphenyl)-2',4'-pentadieno yl¿ aminoethyl]-4-diphenylmethoxypiperidine, CAS 110501-66-1) to inhibit leukotriene production and to antagonize the effect of histamine was examined in comparison with the ability of azelastine, an antiallergic drug having an antihistamine activity. Linetastine and its active metabolite TMK777 (1-[¿5'-(3"-methoxy-4"-hydroxyphenyl)-2',4'-pentadienoyl¿ aminoethyl]-4-diphenylmethoxypiperidine, CAS 101619-11-8) inhibited the release of leukotrienes B4 and C4 from calcium ionophore-stimulated human leukocytes. The respective IC50 values of leukotriene B4 were 1.2 x 10(-7) mol/l and 8.6 x 10(-8) mol/l, and those of leukotriene C4 were 1.5 x 10(-7) mol/l and 7.1 x 10(-8) mol/l. Azelastine also inhibited the release of leukotriene B4 and C4, but its IC50 values were higher than 1 x 10(-5) mol/l. Linetastine at 1-10 mg/kg p.o. inhibited the increase in leukotriene B4 and C4 production in the lungs during late asthmatic responses in actively sensitized guinea-pigs. The effect of 3.2 mg/kg lasted for more than 16 b. Since repeated oral administration of linetastine, 1 mg/kg once a day for 7 successive days, showed the same inhibitory effect on the increase in respiratory resistance and the leukotriene production as single oral administration, the effect of linetastine was neither tachyphylactic nor cumulative. Azelastine at 10 mg/kg had no effect on the leukotriene production. Linetastine TMK777 and azelastine dose-dependently inhibited the histamine-induced contraction of isolated guinea-pig trachea in a noncompetitive manner, the respective pD2 values were 7.28, 7.98 and 8.07. Linetastine inhibited histamine-induced bronchoconstriction dose-dependently at 1-10 mg/kg (p.o.) in guinea-pigs, and the effect lasted for more than 24 h. Repeated oral administration of linetastine, 0.32 to 3.2 mg/kg once a day for 7 successive days inhibited the histamine-induced bronchoconstriction, the same as single oral dosing. Azelastine at 0.32 mg/kg p.o. also showed antihistamine activity. In conclusion, linetastine inhibits both the production of leukotrienes and the effect of histamine at almost the same dose and the effects were long lasting.
将利奈司汀(TMK688,1 - [5' - (3'' - 甲氧基 - 4'' - 乙氧基羰基氧基苯基) - 2',4' - 戊二烯基]氨基乙基 - 4 - 二苯甲氧基哌啶,CAS 110501 - 66 - 1)抑制白三烯生成以及拮抗组胺作用的能力,与具有抗组胺活性的抗过敏药物氮卓斯汀的能力进行了比较研究。利奈司汀及其活性代谢产物TMK777(1 - [5' - (3'' - 甲氧基 - 4'' - 羟基苯基) - 2',4' - 戊二烯酰]氨基乙基 - 4 - 二苯甲氧基哌啶,CAS 101619 - 11 - 8)抑制了钙离子载体刺激的人白细胞中白三烯B4和C4的释放。白三烯B4的各自IC50值分别为1.2×10(-7)mol/L和8.6×10(-8)mol/L,白三烯C4的IC50值分别为1.5×10(-7)mol/L和7.1×10(-8)mol/L。氮卓斯汀也抑制白三烯B4和C4的释放,但其IC50值高于1×10(-5)mol/L。口服1 - 10mg/kg的利奈司汀抑制了主动致敏豚鼠迟发性哮喘反应期间肺中白三烯B4和C4生成的增加。3.2mg/kg的作用持续超过16小时。由于连续7天每天一次口服1mg/kg的利奈司汀对呼吸阻力增加和白三烯生成的抑制作用与单次口服相同,利奈司汀的作用既不是快速耐受性的也不是累积性的。10mg/kg的氮卓斯汀对白三烯生成没有影响。利奈司汀、TMK777和氮卓斯汀以非竞争性方式剂量依赖性地抑制组胺诱导的离体豚鼠气管收缩,各自的pD2值分别为7.28、7.98和8.07。利奈司汀在1 - 10mg/kg(口服)剂量下剂量依赖性地抑制豚鼠组胺诱导的支气管收缩,且作用持续超过24小时。连续7天每天一次口服0.32至3.2mg/kg的利奈司汀抑制组胺诱导的支气管收缩,与单次口服给药相同。口服0.32mg/kg的氮卓斯汀也显示出抗组胺活性。总之,利奈司汀以几乎相同的剂量抑制白三烯的生成和组胺的作用,且作用持久。