Abstract
We have investigated the ability of compound 48 80 and of histamine H 1 and H 2 receptor antagonists to inhibit toluene diisocyanate-induced contractions in isolated guinea-pig bronchi. Compound 48 80 (100 μg/ml) significantly inhibited toluene diisocyanate-induced contractions. By contrast, the two histamine H 1 and H 2 receptor antagonists, chlorpheniramine (10 μM) and cimetidine, (10 μM) did not affect toluene diisocyanate-induced contractions, but significantly inhibited contractions induced by exogenously applied histamine (100 μM) and by 48 80 . We investigated which mechanisms 48 80 used to inhibit toluene diisocyanate-induced contractions, paying particular attention to the possible involvement of capsaicin-sensitive primary afferents. In vitro capsaicin desensitization (10 μM for 30 min followed by washing) significantly reduced compound 48 80 - induced contractions. A capsaicin-resistant component of contraction was also evident. Ruthenium red (3 μM), an inorganic dye which acts as a selective functional antagonist of capsaicin, did not affect 48 80 - induced contraction. MEN 10,207 (Tyr 5, D-Trp 6,8,9,Arg 10)-neurokinin A A (4–10) (3 μM) a selective antagonist of NK 2-tachykinin receptors significantly reduced 48 80 - induced contractions. These results show that compound 48 80 inhibits toluene diisocyanate-induced contractions in isolated guinea-pig bronchi. It is likely that two mechanisms are involved in the inhibition: (1) the release of mediators other than histamine by mast cells, (2) an effect of 48 80 on sensory nerves.
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More From: European Journal of Pharmacology: Environmental Toxicology and Pharmacology
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