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J. Venom. Anim. Toxins incl.Trop. Dis. V.13, n.1, p.250, 2007. IX Symposium of the Brazilian Society on Toxinology. Poster - ISSN 1678-9199. |
DO PERIPHERAL NK1 RECEPTOR AND SUBSTANCE P PLAY AN IMPORTANT ROLE IN Phoneutria nigriventer VENOM-INDUCED ITCH IN THE MICE DORSAL SKIN?
COSTA S.K. (1), STARR A. (2), HYSLOP S. (3), GILMORE D. (2), BRAIN S.D. (2)
(1) Department of Pharmacology (ICB-I), University of São Paulo, São Paulo, Brazil; (2) Cardiovascular Division, King's College London, UK; (3) Department of Pharmacology (FCM, UNICAMP), Campinas-SP
Pain and itch sensations are induced by depolarization of C-fibre nerves and possibly other types of fibres. We have evidence from several species, including mice, that skin plasma extravasation induced by the Phoneutria nigriventer spider venom (PNV) is dependent on tachykinin NK1 receptors. We have now investigated the itching measured as bouts of scratching in response to intradermal (i.d.) PNV in wildtype (WT) and NK1 receptor knockout (KO) mice. Mice were given a single i.d. injection (0.05 ml) of test agent or vehicle into the shaved dorsal skin, in the intercostal region, in a randomized way. The bouts of scratching were recorded in a blinded manner for 60 min. Oedema formation was concomitantly assessed by the extravascular accumulation of 125I-albumin. The i.d. injection of either substance P (at a high dose of 100 nmol/site) or PNV (0.3-10 mg/site) induced oedema formation in WT but substantially less was observed in NK1 KO mice, as previously reported. PNV also induced scratching, but significantly less scratching was observed in NK1 KO with WT mice. In contrast, SP did not induce significant scratching at amounts up to 100 nmol in WT mice. Experiments with an NK1 receptor antagonist SR140333 (at doses that blocked PNV-induced oedema) revealed that whilst a local co-injection (1 nmol) in WT mice had no effect on PNV (3 mg/site)-induced scratching (18.5 ± 3.7 vs. 14.4 ± 3.5 bouts, mean ± S.E.M., n=5-7), systemic treatment with SR140333 (120 nmol/kg, i.v.) significantly inhibited scratching (14 ± 3.5 vs. 3.1 ±1.2* bouts, n=4-6). These results indicate that NK1 receptors are involved in mediating PNV-induced scratching and that the location of the receptors is unlikely to be skin. Thus, a distinct separation between endogenous microvascular and PNV nociceptive NK1-dependent effects is suggested.
KEY WORDS: Phoneutria nigriventer, spider, itch, NK1 receptor, oedema
FINANCIAL SUPPORT: BHF (U.K.), CNPq, FAPESP
CORRESPONDENCE TO: S Costa. Dept of Pharmacology, ICB-USP, Phone: (+55) 11-30917320. E-mail: scosta@icb.usp.br