Abstract
1 The site of action of substance P and related tachykinins with respect to isotonic contractions was examined on the isolated muscularis mucosae attached to the submucous plexus of the guinea-pig oesophagus. 2 Substance P (> 30 nm) produced a concentration-dependent contraction of the muscularis mucosae (EC50 1.9 ± 0.5 μm, n = 10). The contractions were rapid in onset (2 min or less), sustained, reversible by washing and the preparation did not show tachyphylaxis. 3 Eledoisin and physalaemin produced similar sustained contraction of the muscularis mucosae. The order of sensitivity was eledoisin > substance P > physalaemin. Contractions induced by 1 μm of each tachykinin were not significantly modified by incubation of the tissue with substance P or eledoisin (10 μm for 30 min). 4 The contractile responses to tachykinins were unaffected by tetrodotoxin (0.3 μm), atropine (0.3 μm), phentolamine (1 μm), chlorpheniramine (1 μM), methysergide (1 μM) baclofen (100 μm) and verapamil (10 μm), but were abolished by the incubation of the tissue with calcium-free, EGTA (0.1 mm)-containing Tyrode solution. 5 A substance P antagonist, [d-Pro2, d-Trp7,9]-substance P (>0.1 μm), produced a transient contraction of the muscularis mucosae and the smooth muscle regained its original tone within 6 to 10 min. Contractions to the tachykinins were now inhibited by the antagonist (0.1–10 μm) in a concentration-dependent manner, the order of sensitivity being physalaemin > substance P = eledoisin. 6 The cholinergically mediated electrically (0.1 Hz, 0.5 ms, supramaximal voltage)-induced twitch contractions of the muscularis mucosae were not significantly modified by substance P (0.01–0.3 μm). 7 The present results indicate that substance P and related tachykinins contract the isolated muscularis mucosae of the guinea-pig oesophagus by a direct action on the smooth muscle, probably by stimulating SP-E receptors.