THE COMPARATIVE ACTIONS AND ADVERSE EFFECT PROFILE OF SINGLE DOSES OF H(1)-RECEPTOR ANTIHISTAMINES IN THE AIRWAYS AND SKIN OF SUBJECTS WITH ASTHMA

被引:51
作者
WOODBAKER, R [1 ]
HOLGATE, ST [1 ]
机构
[1] SOUTHAMPTON GEN HOSP,DEPT IMMUNOPHARMACOL,SOUTHAMPTON SO9 4XY,HANTS,ENGLAND
关键词
ANTIHISTAMINES; ASTHMA; H(1)-RECEPTOR ANTAGONISTS;
D O I
10.1016/0091-6749(93)90213-Y
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: The development of potent H-1-receptor antagonists that are free of adverse effects has renewed interest in their use in the treatment of asthma. Methods: We performed a study of the action of chlorpheniramine, terfenadine, brompheniramine, cetirizine, cyproheptadine, clemastine, and astemizole compared with placebo on histamine-induced skin wheals and bronchoconstriction in a single group of patients with asthma. Another group underwent methacholine bronchoprovocation. Results: Antihistamine pretreatment increased mean baseline measurements of forced expiratory volume in 1 second (FEV1) between 2.58% and 9.28% compared with placebo, which was significant for all drugs except brompheniramine and clemastine. Compared with placebo, all antihistamines provided significant protection against histamine-induced bronchoconstriction when measured as the provocation concentration required to cause a 20% fall in FEV1; terfenadine and cetirizine provided significantly greater protection than other antihistamines. Protection against histamine-induced skin wheals, measured as the slope of the log concentration-response curve, was only significant for the new drugs, terfenadine and cetirizine. There was a good correlation between the protective effect of the drugs in the skin and airways (r = 0.85; p < 0.01). No significant difference in methacholine provocation concentration required to cause a 20% fall in FEV1 values between treatments was found. Conclusions: The new H-1-receptor antagonists terfenadine and cetirizine provided significantly better protection than the older antihistamines against the action of histamine in the skin and airways. None of the antihistamines showed evidence of anticholinergic activity in the asthmatic airways at the doses studied.
引用
收藏
页码:1005 / 1014
页数:10
相关论文
共 39 条
[31]   TERFENADINE, A POTENT HISTAMINE H1-RECEPTOR ANTAGONIST IN THE TREATMENT OF GRASS-POLLEN SENSITIVE ASTHMA [J].
RAFFERTY, P ;
JACKSON, L ;
SMITH, R ;
HOLGATE, ST .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1990, 30 (02) :229-235
[32]   THE PHARMACOKINETICS AND ANTIHISTAMINIC EFFECTS OF BROMPHENIRAMINE [J].
SIMONS, FER ;
FRITH, EM ;
SIMONS, KJ .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1982, 70 (06) :458-464
[33]  
SIMONS FER, 1990, J ALLERGY CLIN IMMUN, V86, P540
[34]  
STERNBERG L, 1948, Ann Allergy, V6, P569
[35]  
THAM R, 1978, ARZNEIMITTEL-FORSCH, V28-1, P1017
[36]   COMPARISON OF THE EFFECT OF LORATADINE ON THE AIRWAY AND SKIN-RESPONSES TO HISTAMINE, METHACHOLINE, AND ALLERGEN IN SUBJECTS WITH ASTHMA [J].
TOWN, GI ;
HOLGATE, ST .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1990, 86 (06) :886-893
[37]  
WEINER M, 1982, ARZNEIMITTEL-FORSCH, V32-2, P1193
[38]   DOSE-RESPONSE RELATIONSHIP OF THE H1-HISTAMINE ANTAGONIST, EBASTINE, AGAINST HISTAMINE AND METHACHOLINE-INDUCED BRONCHOCONSTRICTION IN PATIENTS WITH ASTHMA [J].
WOODBAKER, R ;
HOLGATE, ST .
AGENTS AND ACTIONS, 1990, 30 (1-2) :284-286
[39]  
WOODWARD JK, 1982, ARZNEIMITTEL-FORSCH, V32-2, P1154