Fukuda T, Saito T, Tajima S, Shimohara K, Ito K
Arzneimittelforschung. 1984;34(7):805-10.
Antiallergic effects of 1-(2-ethoxyethyl)-2-(4-methyl-1-homopiperazinyl)benzimidazol e difumarate (KB-2413) were investigated in immediate type hypersensitivities. KB-2413 (0.005-0.04 mg/kg p.o.) showed a marked inhibition on lethal anaphylaxis in guinea pigs induced by anti-egg albumin rabbit serum, and it was 30 and 1.6 times more potent than chlorpheniramine and ketotifen, respectively. KB-2413 (0.003-0.1 mg/kg p.o.) showed a dose-dependent inhibition on vascular permeability increase induced by 48 h homologous passive cutaneous anaphylaxis (PCA) and histamine in guinea pigs, being about 10-30 times and 3 times more potent than chlorpheniramine and ketotifen, respectively. All drugs did not completely inhibit 4 h heterologous PCA in guinea pigs induced by the anti-egg albumin rabbit serum in the doses used here, but KB-2413 was more effective than chlorpheniramine and ketotifen. No difference in inhibitory effect on the vascular permeability increase between the single and daily oral administration for 4 weeks of KB-2413 could be found. KB-2413, as well as chlorpheniramine and ketotifen, showed a dose-dependent inhibition on 48 h homologous PCA in rats at doses of 1-10 mg/kg p.o., and showed a concentration-dependent inhibition on Schultz-Dale reaction at 10(-8) - 10(-7) mol/l. KB-2413 (10(-5) - 10(-3) mol/l) showed a concentration-dependent inhibition of anaphylactic histamine release from isolated rat peritoneal mast cells which were passively sensitized by rat IgE. KB-2413 also inhibited compound 48/80-induced histamine release from rat peritoneal mast cells.(ABSTRACT TRUNCATED AT 250 WORDS)
研究了1-(2-乙氧基乙基)-2-(4-甲基-1-高哌嗪基)苯并咪唑二富马酸盐(KB-2413)在速发型超敏反应中的抗过敏作用。KB-2413(0.005-0.04mg/kg口服)对豚鼠由抗卵清蛋白兔血清诱导的致死性过敏反应有显著抑制作用,其效力分别比氯苯那敏和酮替芬强30倍和1.6倍。KB-2413(0.003-0.1mg/kg口服)对豚鼠48小时同源被动皮肤过敏反应(PCA)和组胺诱导的血管通透性增加呈剂量依赖性抑制,效力分别比氯苯那敏和酮替芬强约10-30倍和3倍。在此所用剂量下,所有药物均未完全抑制豚鼠由抗卵清蛋白兔血清诱导的4小时异源PCA,但KB-2413比氯苯那敏和酮替芬更有效。未发现KB-2413单次口服和每日口服4周对血管通透性增加的抑制作用有差异。KB-2413以及氯苯那敏和酮替芬在1-10mg/kg口服剂量下对大鼠48小时同源PCA呈剂量依赖性抑制,在10(-8)-10(-7)mol/l时对舒尔茨-戴尔反应呈浓度依赖性抑制。KB-2413(10(-5)-10(-3)mol/l)对经大鼠IgE被动致敏的离体大鼠腹腔肥大细胞的过敏性组胺释放呈浓度依赖性抑制。KB-2413还抑制化合物48/80诱导的大鼠腹腔肥大细胞组胺释放。(摘要截短至250字)