The contractile effect of substance P, neurokinin A, carbachol and serotonin (5-HT) on isolated Fischer 344 rat trachea was studied. Contractions of two distal tracheal rings were measured isometrically in a 2-ml organ bath. Cumulative concentration-response curves were obtained for carbachol (EC 5 0 ring 1: 1.6 10 - 7 M and ring 2: 2.2 10 - 7 M) and for 5-HT (EC 5 0 ring 1: 10.2 10 - 7 M and ring 2: 10.5 10 - 7 M). Non-cumulative administration of substance P and neurokinin A (10 - 8 to 10 - 5 M) caused a concentration-dependent contraction with an EC 5 0 ( 10 - 7 M) of 1.10 ± 0.27 and 1.97 ± 0.45 respectively. The maximal contraction was 32.6 ± 2.5% (substance P) and 32.6 ± 1.5% (neurokinin A) of the maximal contraction with carbachol. In contrast, neither substance P nor neurokinin A caused contraction of trachea from BDE rats. The tachykinin NK 1 receptor agonist, Ac[Arg 6 ,Sar 9 , Met(O 2 ) 1 1 ]substance P-(6-11), caused a concentration-dependent contraction with an EC 5 0 ( 10 - 9 M) of 1.38 ± 0.09 and a maximal effect of 25.5 ± 2.1% of the maximal contraction with carbachol. The tachykinin NK 2 receptor agonist, [β-Ala 8 ]neurokinin A-(4-10), had a small contractile effect at 10 - 6 M (8.4 ± 0.8% of the maximal contraction with carbachol) while the tachykinin NK 3 receptor agonist, senktide, had no effect up to 3.3 10 - 6 M. The tachykinin NK 1 receptor antagonist, (±)-RP67580 ((3AR,7aR)-(7,7-diphenyl-2-(1-imino-2-(2-methoxyphenylethyl)-perhydraisoinot ol-4-one))) (3 10 - 9 to 10 - 7 M), produced a concentration-dependent rightward shift of the concentration-response curve for neurokinin A (Schild plot: slope 1.13, x-intercept 8.4). The tachykinin NK 2 receptor antagonist, SR48968 ((S)-N-methyl-N[4-(4-acetylamine-4-phenylpiperidino)-2-(3,4-dichlorophenyl) butylbenzamide) (10 - 8 to 10 - 6 M), had no major effect on the concentration-response for neurokinin A. We conclude that substance P and neurokinin A contract Fischer 344 rat trachea mainly by interaction with a tachykinin NK 1 receptor.