Why the study?
Does intranasal administration of CV-11974 or PD123319 reduce antigen-induced airway hyperresponsiveness and inflammation in guinea pigs?
Does intranasal administration of CV-11974 or PD123319 reduce antigen-induced airway hyperresponsiveness and inflammation in guinea pigs?
Intranasal administration of the AT1 receptor antagonist CV-11974 reduces antigen-induced airway hyperresponsiveness in a guinea pig model of asthma.
BACKGROUND: Angiotensin II is a putative mediator in asthma, but the effect of topical administration of type 1 angiotensin II (AT1) receptor antagonists on allergic airway reactions is not known. OBJECTIVE: To investigate the effect of intranasal administration of CV-11974, an AT1 receptor antagonist, and of PD123319, a type 2 angiotensin II (AT2) receptor antagonist, on antigen-induced airway reactions in guinea pigs. METHODS: Thirty minutes after intranasal topical administration of CV-11974 (0.1 or 1.0 mg/ml) or PD123319 (10 mg/ml) into the airways, the animals were given an antigen challenge. Airway hyperresponsiveness and bronchoalveolar lavage fluid were analyzed 24 h after the antigen challenge. RESULTS: Although these compounds did not inhibit antigen-induced early-phase bronchoconstriction or late-phase airway eosinophilia, intranasal administration of CV-11974 (but not PD123319) inhibited antigen-induced airway hyperresponsiveness in a dose-dependent manner 24 h after the antigen challenge. CONCLUSION: Intranasal administration of an AT1 receptor antagonist reduces antigen-induced airway hyperresponsiveness.
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Myou et al. (2002) studied this question.
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