Pre-junctional α2-adrenoceptor activity of B-HT920

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Abstract
An in-vitro study has been carried out on the pre-junctional α2-adrenoceptor activity of the thiazoloazepine derivative B-HT 920 (6-allyl-2-amino-5,6,7,8-tetrahydro-4H-thiazolo-[4,5-d]-azepine) using isolated, field-stimulated rat vas deferens and guinea-pig ileum. The α2-selective agonists clonidine (an imidazoline derivative) and α-methyl noradrenaline (a β-phenethylamine derivative) were compared. Results show that B-HT 920 is a potent agonist on pre-junctional α2-adrenoceptors and is competitively antagonized by the selective α2-adrenoceptor antagonist yohimbine. The characteristics of the pharmacological responses obtained with B-HT920 indicate that it interacts with the receptor in an imidazoline-like, rather than a β-phenethylamine-like, manner.