ISSN:
1432-1912
Keywords:
Acetylsalicylic acid
;
Bronchial obstruction
;
Guinea pigs
;
Histamine aerosol
;
Histamine receptor antagonists
;
Prostacyclin aerosol
;
Platelets
;
Thromboxane synthetase inhibitors
Source:
Springer Online Journal Archives 1860-2000
Topics:
Medicine
Notes:
Summary Groups of 6–15 guinea pigs sensitized to ovalbumin were challenged by repeated inhalations of a constant histamine dose at time 0, 10, 20, 60 and 70 min. Bronchial obstruction was measured by whole body plethysmography. The degree of bronchial obstruction increased from one challenge to the other reaching maximal values after 70 min. This increase of bronchial responsiveness to histamine after repeated histamine challenges was reduced by pretreatment with clemastine (histamine H1-receptor antagonist, 0.12 mg/kg i.p., n=7, P〈0.05) and more effectively by combined clemastine/cimetidine pretreatment (combined H1-H2-receptor antagonists, 0.12 resp. 10 mg/kg, n=7, P〈0.001); pretreatment with acetylsalicyclic acid (10 mg/kg orally) accelerated the increase of bronchial responsiveness to histamine (n=9, P〈0.01 at the second challenge), inhalation of prostacyclin (1 μg) prior to each histamine inhalation prevented the increase of bronchial histamine sensitivity totally (n=10, P〈0.001), whereas inhibition of thromboxane biosynthesis (imidazol, 10 mg/kg i.p., n=6; 4-[2-(1H-imidazol-1-yl)ethoxy]benzoic acid, 10 mg/kg i.p., n=9; imidazo(1,5-a)pyridine-5-hexanoic acid, 1 mg/kg i.p., n=8) as well as immunologic platelet depletion were ineffective in our test system. We conclude that prostacyclin inhibits the increase of bronchial responsiveness to histamine after sequential histamine inhalation challenges by a platelet independent mechanism. 1-(3-phenyl-2-propenyl)-1H-imidazol, the fourth type of thromboxane synthetase inhibitor tested (10 mg/kg i.p., n=15) showed specific effects which may be attributed to antihistamine functions.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1007/BF00500910
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