Abstract

Norepinephrine (NE) elicited a saturable, concentration-dependent contraction in rat aortic strips (EC50, 9 nM). Phenoxybenzamine (PBZ) inhibited, irreversibly, the NE-induced contraction (max. inhibition at 50 nM applied for 10 min.). The protection of the α-receptor by NE showed a biphasic concentration dependence. These results are interpreted in terms of a 2-receptor model.

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