Kamali F, Emanuel M, Rawlins M D
Department of Pharmacological Sciences, The University, Claremont Place, Newcastle Upon Tyne.
Eur J Clin Pharmacol. 1991;40(1):83-5. doi: 10.1007/BF00315144.
The antihistaminic effects of 7 days treatment with each of three doses of noberastine (10, 20 and 30 mg) were compared to placebo in 12 healthy male volunteers. The antihistaminic activity was assessed from the inhibition of weal and flare formation after intradermal histamine injections. For both weal and flare there was a highly significant effect of treatment with each of the three doses of noberastine, compared to placebo. The 30 mg daily dose produced the maximum inhibition of weal and flare. The daily mean values for the assessment of sedation by visual analogue scales at 09.00 h, 15.00 h and 21.00 h showed no significant treatment, or order, effect for any of the three doses of noberastine compared to placebo. The mean steady-state plasma concentrations of noberastine were significantly higher with increasing daily doses of noberastine (trough concentrations: 1.0, 1.6 and 2.2 ng.ml-1; peak concentrations: 3.5, 13.4 and 20.9 ng.ml-1 for 10, 20 and 30 mg daily dose, respectively). The percentage weal inhibition correlated (r = 0.77) with steady-state noberastine plasma trough levels. The percentage flare inhibition showed a weaker correlation (r = 0.35) with steady-state noberastine plasma trough levels.
在12名健康男性志愿者中,比较了三种剂量(10毫克、20毫克和30毫克)的诺贝司汀连续7天治疗的抗组胺作用与安慰剂的效果。通过皮内注射组胺后对风团和红晕形成的抑制来评估抗组胺活性。与安慰剂相比,三种剂量的诺贝司汀治疗对风团和红晕均有高度显著的效果。每日30毫克剂量对风团和红晕的抑制作用最大。在09:00、15:00和21:00通过视觉模拟量表评估镇静的每日平均值显示,与安慰剂相比,三种剂量的诺贝司汀在治疗或给药顺序方面均无显著效果。随着诺贝司汀每日剂量的增加,其平均稳态血浆浓度显著升高(谷浓度:每日10毫克、20毫克和30毫克剂量分别为1.0、1.6和2.2纳克/毫升;峰浓度:分别为3.5、13.4和20.9纳克/毫升)。风团抑制百分比与诺贝司汀稳态血浆谷浓度相关(r = 0.77)。红晕抑制百分比与诺贝司汀稳态血浆谷浓度的相关性较弱(r = 0.35)。