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The role of calcium in phorbol-12,13-dibutyrate (PDB)-induced contractions of the canine saphenous vein (CSV) was examined. Phorbol-12,13-dibutyrate elicited concentration-dependent contractions in CSV (EC50 = 1.6 +/- 0.2 X 10(-7) M) which were not affected by atropine (10(-6) M), pyrilamine (10(-6) M), and phentolamine (10(-5) M). The maximum contraction induced by PDB (10(-6) M) was slightly greater than that elicited by phenylephrine (PE; 10(-4) M). Phorbol-12,13-dibutyrate produced maximal 45Ca2+ uptake (0.80 +/- 0.07 mmol/kg wet wt) comparable with that induced by PE (0.90 +/- 0.04 mmol/kg wet wt) which was approximately fourfold above basal 45Ca2+ uptake (0.21 +/- 0.02 mmol/kg wet wt). The increase in 45Ca2+ uptake stimulated by PDB and PE was completely abolished by La3+ (5 mM). In the absence of Ca2+ entry, the contractions to PDB were reduced by only 29 +/- 3.4%. Substantial responses to PDB (51.3 +/- 4.8% of control) remained after reduction of intracellular Ca2+ store by repeated challenges with PE (10(-4) M) in the presence of La3+. Similar results were obtained when the contractions of CSV to PDB were determined in zero external Ca2+ medium. The data suggest that PDB utilizes both extracellular and intracellular Ca2+ for contractions of CSV.

The effects of calcium entry blockade on the vasoconstriction to the selective alpha-1 adrenoceptor agonists d- and I-SK&F 89748-A (1,2,3,4-tetrahydro-8-methoxy-[5-methylthiol] -2-naphthalenamine HCl) in pithed rats and in rat and guinea-pig isolated aortas were studied. The log-dose response curves for the increase in diastolic pressure in pithed rats to i.v. injections of both enantiomers of SK&F 89748-A were maximally shifted only 5-fold to the right after pretreatment of the animals with nifedipine (1 or 3 mg/kg i.a.) or l-verapamil (0.3 or 1 mg/kg i.a.), showing the relative insensitivity of the vasopressor responses to SK&F 89748-A to these calcium entry blockers. In the rat isolated aorta, the contractile responses to the l-enantiomer of SK&F 89748-A were significantly more susceptible to calcium entry blockade with l-verapamil, nifedipine and D600 than the d-isomer. The contractions of the guinea-pig isolated aorta to both isomers proved highly insensitive to calcium slow channel blockade by D600. These results indicate that the contractions of vascular smooth muscle in pithed rats in vivo and of guinea-pig isolated aortas in vitro initiated by the d-and l-isomers of SK&F 89748-A are largely dependent upon processes not requiring an influx of extracellular calcium. The differential sensitivity to calcium entry blockade of the contractile responses of rat isolated aortas to the d- and l-isomers of SK&F 89748-A may reflect different ways of interaction of both enantiomers with the alpha-l adrenoceptor on rat aorta.

The pressor activity of the 1-enantiomer of SK & F 89748-A, 1,2,3,4-tetrahydro-8-methoxy-5-(methylthio)-2-naphthalenamine, in pithed normotensive rats was found comparable with that of 1-phenylephrine. The d-enantiomer was half as potent. The log dose-pressor effect curves for d- and 1-SK & F 89748-A were not influenced by reserpine treatment (2 X 5 mg/kg i.p., -48 and -24 h), were virtually unaffected by yohimbine (1 mg/kg i.v., -15 min) but were markedly shifted to the right by prazosin (0.1 mg/kg i.v., -15 min) and phentolamine (1 mg/kg i.v., -15 min). Similar observations were made for the 1-enantiomer in pithed cats. It is concluded that d- and 1-SK & F 89748-A are potent, directly acting highly selective agonists of (vascular) postjunctional alpha 1-adrenoceptors. Potency and selectivity were equally pronounced for both enantiomers. The currently available selective agonists of alpha 1-adrenoceptors, including the optical isomers of SK & F 89748-A, cannot distinguish between alpha 1- and alpha 2-adrenoceptors. This conclusion is based on binding affinity since these affinities are linearly correlated as shown by radioligand displacement experiments.