Niemegeers C J, Awouters F, Janssen P A
Agents Actions. 1986 Apr;18(1-2):141-4. doi: 10.1007/BF01988005.
In the compound 48/80 lethality test in rats, which is based on the specific activation of mast cells, astemizole was selected as a potent, long-acting and orally very effective inhibitor of anaphylactoid shock. In comparison to other histamine-H1 antagonists astemizole was also a very effective inhibitor of allergic reactions in rats and dogs and remarkably free of non-specific interactions with other biological amines and normal body functions. In numerous tests no evidence of central activity was found and toxicity studies have shown astemizole to be a very safe drug despite of its long duration of action. A daily dose of 10 mg of astemizole was found clinically free of side-effects and more effective than conventional antihistamine treatment.
在基于肥大细胞特异性激活的大鼠复合48/80致死性试验中,阿司咪唑被选为类过敏性休克的一种强效、长效且口服非常有效的抑制剂。与其他组胺H1拮抗剂相比,阿司咪唑也是大鼠和犬类过敏反应的非常有效的抑制剂,并且与其他生物胺和正常身体功能无明显非特异性相互作用。在众多试验中未发现中枢活性的证据,毒性研究表明,尽管阿司咪唑作用持续时间长,但它是一种非常安全的药物。临床发现,每日服用10毫克阿司咪唑无副作用,且比传统抗组胺治疗更有效。