Abstract

The contractile activities of neurokinin A (NKA), neurokinin B (NKB) and related peptides on the guinea-pig ileum, rat vas deferens and rat duodenum were compared to the activity of substance P (SP). The potencies of NKA and NKB on the guinea-pig ileum (SP-P tissue) were nearly the same as that of SP. NKA was approximately 250–400 times more potent than SP on the rat vas deferens ( EC 50 = 59.5 nM; SP, EC 50 = 1500 nM ) and rat duodenum ( EC 50 = 1.8 nM; SP, EC 50 = 674 nM ) (SP-E tissues). NKB also showed high contracting activity on the rat duodenum ( EC 50 = 3.1 nM ) but was 10 fold less active than NKA on the rat vas deferens. These results suggest that neurokinin peptides are possible endogenous agonists for the SP-E tissues. The contractile potency of NKA and NKB remained nearly complete after removal of N-terminal tripeptide portions, i.e., His-Lys-Thr and Asp-Met-His from the native peptides, respectively. However, the removal of the Asp residue from both NKA7 and NKB7 decreased activity until it was similar to that of SP.

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