Facial thermography is a sensitive tool to determine antihistaminic activity: comparison of levocetirizine and fexofenadine

被引:16
作者
Larbig, Michael
Burtin, Bernard
Martin, Laurent
Stamm, Holger
Luettig, Birgit
Hohlfeld, Jens M.
Krug, Norbert
机构
[1] Fraunhofer Inst Toxicol & Exp Med, D-30625 Hannover, Germany
[2] UCB Bioprod SA, Pharma Sector, Braine Lalleud, Belgium
关键词
facial thermography; fexofenadine; healthy subjects; levocetirizine; nasal histamine provocation; nasal skin temperature; wheal and flare;
D O I
10.1111/j.1365-2125.2006.02647.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Aims To assess the antihistaminic activity of levocetirizine and fexofenadine 2 h and 24 h after drug administration using facial thermography and to compare the results with those using well-established parameters of antihistaminic activity in the nose and skin. Methods This was a randomized, double-blind, three-treatment, three-period, single-dose, cross-over study in healthy males taking levocetirizine 5 mg, fexofenadine 120 mg or placebo. The primary endpoint was nasal skin temperature after nasal histamine challenge recorded for 20 min at 2 and 24 h after drug intake. The secondary endpoints were nasal symptoms and a histamine skin prick test. Results Thirty subjects were randomized. At 2 h after drug intake the inhibition of the nasal temperature increase from baseline was not significantly different between levocetirizine and fexofenadine. At 24 h it was significantly more pronounced after levocetirizine than fexofenadine (difference: least-squares mean: -0.13 degrees C; P <= 0.024, 95% CI -0.24, -0.02). Both drugs significantly reduced (P <= 0.001) the mean temperature increase from baseline compared with placebo at 2 and 24 h (least-squares mean increase and (95% CI): levocetirizine, -0.28 degrees C (-0.42, -0.14) and -0.32 degrees C (-0.43, -0.21); fexofenadine -0.35 degrees C (-0.49, -0.21) and -0.19 degrees C (-0.30, -0.08), respectively). Results of nasal symptom score and wheal and flare were consistent with the thermography results. Conclusions Facial thermography is an objective, non-invasive and sensitive method to study antihistaminic activity at the nose level. Levocetirizine and fexofenadine demonstrate the same activity at 2 h after drug intake, but levocetirizine has a more sustained activity at 24 h.
引用
收藏
页码:158 / 164
页数:7
相关论文
共 19 条
[1]   Histamine in the immune regulation of allergic inflammation [J].
Akdis, CA ;
Blaser, K .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2003, 112 (01) :15-22
[2]  
BROWN H, 1999, APPL MIXED MODELS ME, P261
[3]   Levocetirizine - A new selective H, receptor antagonist for use in allergic disorders [J].
Day, JH ;
Ellis, AK ;
Rafeiro, E .
DRUGS OF TODAY, 2004, 40 (05) :415-421
[4]   Comparison of the effects of desloratadine and levocetirizine on histamine-induced wheal, flare and itch in human skin [J].
Denham, KJ ;
Boutsiouki, P ;
Clough, GR ;
Church, MK .
INFLAMMATION RESEARCH, 2003, 52 (10) :424-427
[5]   Histamine H1 receptor occupancy and pharmacodynamics of second generation H1-antihistamines [J].
Gillard, M ;
Benedetti, MS ;
Chatelain, P ;
Baltes, E .
INFLAMMATION RESEARCH, 2005, 54 (09) :367-369
[6]   A double-blind, randomized, single-dose, crossover comparison of levocetirizine with ebastine, fexofenadine, loratadine, mizolastine, and placebo: suppression of histamine-induced wheal-and-flare response during 24 hours in healthy male subjects [J].
Grant, JA ;
Riethuisen, JM ;
Moulaert, B ;
DeVos, C .
ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY, 2002, 88 (02) :190-197
[7]   Controlled comparison of the efficacy and safety of cetirizine 10 mg od and fexofenadine 120 mg od in reducing symptoms of seasonal allergic rhinitis [J].
Horak, F ;
Stübner, P ;
Zieglmayer, R ;
Kavina, A ;
De Vos, C ;
Burtin, B ;
Donnelly, F .
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 2001, 125 (01) :73-79
[8]  
Jones B, 2003, DESIGN ANAL CROSS OV, P151
[9]   Relative potency of fexofenadine HCl 180 mg, loratadine 10 mg, and placebo using a skin test model of wheal-and-flare suppression [J].
Kaliner, MA ;
White, MV ;
Economides, A ;
Crisalida, T ;
Hale, M ;
Liao, YN ;
Christian, CD ;
Georges, GC ;
Woodworth, TH ;
Meeves, SG .
ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY, 2003, 90 (06) :629-634
[10]  
MacGlashan Donald Jr., 2003, Journal of Allergy and Clinical Immunology, V112, pS53, DOI 10.1016/S0091-6749(03)01877-3