Mizuno H, Kawamura Y, Iwase N, Ohno H
Central Research Laboratories, SS Pharmaceutical Co., Ltd., Narita, Japan.
Jpn J Pharmacol. 1991 Mar;55(3):321-8. doi: 10.1254/jjp.55.321.
The effects of flutropium on histamine (Hist)-induced increase in intranasal pressure in non-sensitized guinea pigs and nasal mucosa capillary permeability in passively sensitized guinea pigs were investigated. Flutropium (0.3%), atropine (0.3%), diphenhydramine (0.01%) and cimetidine (0.1%) were directly inhaled into the nasal cavities by an ultrasonic nebulizer for 20 min, followed by inhalation of Hist (0.1%) for 10 min. Flutropium, atropine and diphenhydramine had an inhibitory action on the Hist-induced increase in intranasal pressure in guinea pigs. Cimetidine had no effect on this system. In passively sensitized guinea pigs (the challenge was performed 48 hr after sensitization), a 0.1-1.0 mg/kg injection of flutropium (i.v.) dose-dependently inhibited the allergic nasal mucosa capillary permeability. Atropine (10 mg/kg, i.v.) had no inhibitory action on this system. These results suggest that inhalation into the nasal cavities and i.v. injection of flutropium are effective in experimental models of drug- and allergy-induced rhinitis of the guinea pig.
研究了氟托溴铵对未致敏豚鼠组胺(Hist)诱导的鼻内压升高以及对被动致敏豚鼠鼻黏膜毛细血管通透性的影响。通过超声雾化器将氟托溴铵(0.3%)、阿托品(0.3%)、苯海拉明(0.01%)和西咪替丁(0.1%)直接吸入鼻腔20分钟,随后吸入组胺(0.1%)10分钟。氟托溴铵、阿托品和苯海拉明对组胺诱导的豚鼠鼻内压升高具有抑制作用。西咪替丁对该系统无影响。在被动致敏豚鼠中(致敏后48小时进行激发),静脉注射0.1 - 1.0 mg/kg剂量的氟托溴铵可剂量依赖性地抑制过敏性鼻黏膜毛细血管通透性。阿托品(10 mg/kg,静脉注射)对该系统无抑制作用。这些结果表明,鼻腔吸入和静脉注射氟托溴铵在豚鼠药物性和过敏性鼻炎的实验模型中是有效的。