Both α- and α-adrenoceptor subtypes are involved in contractions of rat spleen.

BACKGROUND

The spleen is a reservoir for circulating blood cells, and can contract to expel them.

METHODS

We have investigated the adrenoceptors involved in isometric contractions of rat spleen produced by noradrenaline (NA) and the α-adrenoceptor agonist phenylephrine (Phe).

RESULTS

Contractions to NA were antagonized by both the α-adrenoceptor antagonist prazosin (10 M) and the α-adrenoceptor antagonist yohimbine (10M), and the combination produced further shifts in NA potency. Contractions to Phe were antagonized by prazosin (10 M) which caused a marked parallel shift in the concentration-response curve. High non-selective concentrations of the α-adrenoceptor antagonist BMY7378 (10 M), the α-adrenoceptor antagonist RS100329 ((3 × 10 M), and the putative α-adrenoceptor antagonist cyclazosin (10 M) also produced parallel shifts in the Phe concentration-response curve. BMY7378 at the selective concentration of 3 × 10 M had no effect on responses to Phe, but RS100329 in the selective concentration of 3 × 10 M produced a marked shift in the effects of high concentrations of Phe. Hence, antagonists in concentrations that block both α- and α-adrenoceptors produce approximately parallel shifts in Phe potency.

CONCLUSIONS

Contractions of rat spleen to adrenergic agonists involve α- and α-adrenoceptors, with a lesser role for α-adrenoceptors. This confirms the suggestion that smooth muscle contractions commonly involve multiple subtypes.