Characterization of α 2 ‐adrenoceptors mediating contraction of dog saphenous vein: identity with the human α 2A subtype

• Published in: British journal of pharmacology 2009-02, Vol.121 (8), p.1721-1729
• Main Authors: MacLennan, S. J., Luong, L. A., Jasper, J. R., To, Z. P., Eglen, R. M.
• Format: Article
• Language: English
• ISSN: 0007-1188; 1476-5381
• DOI: 10.1038/sj.bjp.0701296

In the dog saphenous vein α 1 ‐ and α 2 ‐adrenoceptors mediate noradrenaline‐induced contractions in vitro . In order to study the α 2 ‐adrenoceptor in isolation, α 1 ‐adrenoceptors were inactivated by treatment of tissues with the alkylating agent phenoxybenzamine (3.0 μ M for 30 min) in the presence of rauwolscine (1 μ M ) to protect α 2 ‐adrenoceptors. Noradrenaline‐induced contractions of tissues treated with phenoxybenzamine were antagonized competitively by the selective α 2 ‐adrenoceptor antagonist rauwolscine, p K B =8.63±0.07 (means±s.e.mean; n =3), consistent with an interaction at α 2 ‐adrenoceptors. Noradrenaline was a full agonist at α 2 ‐adrenoceptors in dog saphenous vein. By use of the method of partial receptor alkylation and analysis of concentration‐effect curve data by direct, operational model fitting methods, the affinity (p K A ) and efficacy (τ) were 5.74±0.07 and 7.50±1.05, respectively ( n =6). Nine other agonists which were examined each had affinities higher than noradrenaline, but with the exception of the imidazoline, A‐54741 (5,6‐dihydroxy‐1,2,3,4‐tetrahydro‐1‐naphthyl‐imidazoline) had relatively lower efficacies. To compare the α 2 ‐adrenoceptor in dog saphenous vein to the human recombinant subtypes, the affinities of twenty‐one compounds were estimated in functional studies in the dog saphenous vein and in radioligand binding studies for the human α 2A , α 2B and α 2C receptor subtypes expressed in Chinese hamster lung (CHL) cells. Of twenty‐one compounds examined in ligand binding studies, only nine had greater than ten fold selectivity for one human receptor subtype over either of the other two. These compounds were A‐54741, oxymetazoline, guanfacine, guanabenz, prazosin, spiroxatrine, tolazoline, WB 4101 and idazoxan. In dog saphenous vein, their affinities (p K A and p K B for agonists and antagonists respectively) were: A‐54741 (p K A =8.03±0.05), oxymetazoline (p K A =7.67±0.09), guanfacine (p K A =6.79±0.03); guanabenz (p K A =7.02±0.13); prazosin (p K B =5.19±0.08), spiroxatrine (p K B =6.59±0.04), tolazoline (p K B =6.21±0.07), WB 4101 (p K B =7.42±0.09) and idazoxan (p K B =7.11±0.08). Comparisons of affinity estimates for these nine compounds at the receptor in dog saphenous vein and at the human recombinant subtypes suggest that the vascular receptor is most similar to the h α 2A subtype; correlation coefficients ( r ) were 0.82 (h α 2A ), 0.24 (h α 2B ) and 0.04 (h α 2C ). British Journal of Pharmacology (1997