Department of Dermatology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Int Arch Allergy Immunol. 2012;158(2):191-5. doi: 10.1159/000330663. Epub 2012 Jan 26.
Urticaria is mainly caused by mast cell-derived histamine through the histamine H(1) receptor. Antihistamines are occasionally used on demand upon a recurrence of urticaria; therefore, rapidly acting agents should be explored. The onset of action is assumed to depend on time to maximum concentration (T(max)), but the speed of action needs to be evaluated not only through blood concentration analysis but also by measuring in vivo effectiveness.
In this study, we chose two representative second-generation antihistamines (bepotastine and fexofenadine) with relatively short T(max) values and evaluated their effects on histamine-induced skin responses using both visual and laser Doppler imaging scales.
Suppression of histamine-induced flare and itch was observed 3 and 6 h after administration of both antihistamines. Attenuation of itch was seen 30 min after the administration of each drug and thereafter until 6 h. In addition, bepotastine suppressed flare formation after only 30 min following application.
These results suggest that antihistamines suppress histamine-induced itch and flare, followed by wheal formation, and that bepotastine suppresses skin symptoms sooner after administration than fexofenadine does, which is relatively consistent with the T(max) results.
荨麻疹主要由肥大细胞衍生的组胺通过组胺 H(1)受体引起。抗组胺药偶尔在荨麻疹复发时按需使用;因此,应该探索起效迅速的药物。起效时间被认为取决于达到最大浓度的时间(T(max)),但不仅需要通过血液浓度分析,还需要通过测量体内效果来评估作用速度。
在这项研究中,我们选择了两种具有相对较短 T(max)值的代表性第二代抗组胺药(贝他斯汀和非索非那定),并使用视觉和激光多普勒成像量表评估了它们对组胺诱导的皮肤反应的影响。
两种抗组胺药给药后 3 和 6 小时观察到抑制组胺诱导的红斑和瘙痒。在给予每种药物后 30 分钟即可观察到瘙痒减轻,此后直至 6 小时。此外,贝他斯汀在给药后仅 30 分钟即可抑制红斑形成。
这些结果表明抗组胺药抑制组胺诱导的瘙痒和红斑,随后是风团形成,并且贝他斯汀在给药后比非索非那定更快地抑制皮肤症状,这与 T(max)结果相对一致。