Rihoux J P, Van Neste D J
UCB, International Development, Braine-l'Alleud, Brussels, Belgium.
Dermatologica. 1989;179(3):129-34. doi: 10.1159/000248338.
A controlled, randomized, double-blind, crossover study was performed in 10 healthy volunteers to compare changes of cutaneous blood flow values (CBFV) determined by laser Doppler flowmetry before and after intake of a capsule containing either 10 mg cetirizine or 60 mg terfenadine. After the determination of the initial response to the anti-H1 agents, drugs were taken daily (cetirizine 10 mg, terfenadine 120 mg) over a 3-week period and the cutaneous response to histamine and saline was evaluated weekly, exactly 4 h after the last drug intake. The following significant variations were observed (analysis of variance for repeated measurements, p less than 0.05): (1) there is a decrease of histamine-induced wheal and flare under antihistamines (anti-H1), cetirizine being more potent than terfenadine; (2) CBFV, measured on the usual flare area, i.e. at 1 cm of the site of agonist injection, decreased after drug intake. There was a gradual increase of the CBFV inhibition over the 3-week follow-up, cetirizine being more effective than terfenadine, and (3) at the site of agonist injection, reduction of the edematous wheal was associated with significant increases of CBFV after drug intake. This quantitative pharmacologic in vivo assay on the agonist action indicates that at lower doses, cetirizine has a significantly higher anti-H1 activity than terfenadine and that this effect is maintained over a 3-week period. There was no tachyphylaxis.
对10名健康志愿者进行了一项对照、随机、双盲、交叉研究,以比较服用含有10毫克西替利嗪或60毫克特非那定的胶囊前后,通过激光多普勒血流仪测定的皮肤血流值(CBFV)的变化。在确定对抗组胺药的初始反应后,连续3周每天服用药物(西替利嗪10毫克,特非那定120毫克),并在最后一次服药后4小时每周评估对组胺和生理盐水的皮肤反应。观察到以下显著变化(重复测量方差分析,p<0.05):(1)抗组胺药(抗H1)治疗下组胺诱发的风团和潮红减少,西替利嗪比特非那定更有效;(2)在通常的潮红区域(即激动剂注射部位1厘米处)测量的CBFV在服药后降低。在3周的随访中,CBFV抑制作用逐渐增加,西替利嗪比特非那定更有效,并且(3)在激动剂注射部位,服药后水肿性风团的减少与CBFV的显著增加相关。这种对激动剂作用的定量体内药理学测定表明,在较低剂量下,西替利嗪的抗H1活性比特非那定显著更高,并且这种作用在3周内持续存在。没有快速耐受性。