Murata T, Matsumoto Y, Suzuki T, Naito K, Takata I, Tsuzurahara K
Marugo Research Service.
Arerugi. 1997 Jul;46(7):576-84.
We investigated the effect of betotastine besilate (betotastine) on the experimental allergic rhinitis. The oral administration of betotastine (1, 3 and 10 mg/kg) inhibited the increase in dye leakage during and after the nasal perfusion of antigen in actively sensitized rats. It also prevented the increase in intranasal pressure induced by topically applied histamine in non-sensitized guinea pigs. Cetirizine and terfenadine dose-dependently inhibited the increase in a similar manner. Ketotifen (0.01-0.3 mg/kg, p.o.) inhibited the increase more than 50% at 0.01 mg/kg. The ID50s of ketotifen, cetirizine, betotastine and terfenadine for this model were more than 0.01 mg/kg, 0.01 mg/kg, 0.03 mg/kg and 0.5 mg/kg, respectively. Furthermore, in actively sensitized guinea pigs, nasal airway resistance showed a biphasic increase after the topical antigen challenge to the nasal cavity; the first peak at 0.5 hr and a second peak at 4 hr. Both the responses of first and second peaks were significantly inhibited by orally administered betotastine besilate, and its inhibitory effect on the second peak was the strongest among drugs tested. Since betotastine showed significantly inhibitory effects in experimental allergic rhinitis models, it was suggested to show a good efficacy for the treatment of allergic rhinitis clinically.
我们研究了甲磺酸倍他司汀(倍他司汀)对实验性变应性鼻炎的作用。在主动致敏大鼠中,口服倍他司汀(1、3和10mg/kg)可抑制抗原鼻腔灌注期间及之后染料渗漏的增加。它还可防止在未致敏豚鼠中局部应用组胺引起的鼻内压力升高。西替利嗪和特非那定以剂量依赖的方式产生类似的抑制作用。酮替芬(0.01 - 0.3mg/kg,口服)在0.01mg/kg时抑制率超过50%。该模型中酮替芬、西替利嗪、倍他司汀和特非那定的半数抑制剂量(ID50)分别大于0.01mg/kg、0.01mg/kg、0.03mg/kg和0.5mg/kg。此外,在主动致敏的豚鼠中,鼻腔局部抗原激发后气道阻力呈双相增加;第一个峰值出现在0.5小时,第二个峰值出现在4小时。口服甲磺酸倍他司汀可显著抑制第一和第二个峰值的反应,且其对第二个峰值的抑制作用在所测试的药物中最强。由于倍他司汀在实验性变应性鼻炎模型中显示出显著的抑制作用,提示其在临床上对变应性鼻炎的治疗可能具有良好疗效。