Abstract

The effects of substance P on blood flow, plasma extravasation, and knee joint sizes in the rabbit were investigated. Topical bolus application of substance P (1 nmol) onto the exposed rabbit knee joint capsule increased its blood flow from 15 min onwards and reached a peak of 46% at 90 min compared to saline administration. However, administration by the same route and the same dose of the NK 1 receptor agonist [Sar 9, Met (O 2) 11]substance P produced no change on the knee joint blood flow compared to the saline control. The NK 1 receptor antagonist N 2-[(4 R)-4-hydroxy-1-(1-methyl-1 H-indol-3-yl)carbonyl- l-prolyl]- N-methyl- N-phenylmethyl-3-(2-naphthyl)- l-alaninamide (FK888) and the NK 2 receptor antagonist ( S)- N-methyl- N-[4-acetylamino-4-phenylpiperidino)-2-(3,4-dichlorophenyl)-butyl] benzamide (SR48968), at 2×1 nmol and 2×10 nmol, had no effect on the substance P-induced response, which however was reduced by pyrilamine, cimetidine, and flurbiprofen (all at 2×10 nmol). N G-nitro- l-arginine methyl ester ( l-NAME) and N G-nitro- d-arginine methyl ester ( d-NAME), both at 2×100 nmol, did not significantly affect the substance P-induced response. Unilateral intra-articular administration of substance P (1 nmol) into synovial cavities of the rabbit knee joint increased basal blood flow of the ipsilateral joint at 4 h post-injection, and bilateral increase of basal blood flow was observed at 24 h. Plasma extravasation was significantly higher in the substance P-injected knee compared to the contralateral saline-injected knee at 4 h after intra-articular administrations, but not at 24 h. Knee joint sizes were not affected at both time points. The present study is the first to demonstrate that substance P possesses a gradual and persistent vasorelaxant action in the rabbit knee joint. This novel action of substance P is not mediated by NK 1 or NK 2 receptors, but involves histamine and prostaglandins. The degree of plasma extravasation elicited by substance P in the rabbit knee joint is small and short-lived, and with no concurrent oedema of the joint. These results suggest that substance P can evoke acute inflammatory responses in the rabbit knee joint, but on its own, it is unlikely to cause chronic joint inflammation in this species.

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