Abstract
1. Three non-peptide tachykinin receptor antagonists, CP-96,345, RP 67580 and SR 48968, were found to inhibit the electrically-evoked, tachykinin-mediated contractile responses of the rabbit iris sphincter in a concentration-dependent fashion; the pIC50 values were 5.6 +/- 0.01, 5.4 +/- 0.07 and 4.8 +/- 0.03, respectively. 2. These antagonists also inhibited the electrically-evoked, parasympathetic response of the rabbit iris sphincter and the sympathetic response of the guinea-pig vas deferens in a concentration-dependent manner; the pIC50 values were 0.3-1.2 log units lower than those recorded for the tachykinin-mediated responses. 3. Two local anaesthetics, bupivacaine and oxybuprocaine, were also found to inhibit the tachykinin-mediated, cholinergic and sympathetic contractile responses in these tissues in a concentration-dependent manner; the concentration ranges for producing the inhibition were similar to those of the non-peptide tachykinin receptor antagonists. 4. On the sciatic nerves of frogs, the tachykinin receptor antagonists inhibited action potentials in a concentration-dependent manner; the potency of the three drugs was similar to that of bupivacaine. 5. Our results suggest that, in addition to blocking tachykinin receptors, the non-peptide tachykinin receptor antagonists, CP-96,345, RP 67580 and SR 48968, may exert non-specific inhibitory effects on neurotransmission.
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- Advenier C., Rouissi N., Nguyen Q. T., Emonds-Alt X., Breliere J. C., Neliat G., Naline E., Regoli D. Neurokinin A (NK2) receptor revisited with SR 48968, a potent non-peptide antagonist. Biochem Biophys Res Commun. 1992 May 15;184(3):1418–1424. doi: 10.1016/s0006-291x(05)80041-5. [DOI] [PubMed] [Google Scholar]
- Appell K. C., Fragale B. J., Loscig J., Singh S., Tomczuk B. E. Antagonists that demonstrate species differences in neurokinin-1 receptors. Mol Pharmacol. 1992 Apr;41(4):772–778. [PubMed] [Google Scholar]
- Berge O. G., Ståhlberg M. Is the selective non-peptide NK-1 receptor antagonist CP96,345 a peripherally acting analgesic? Regul Pept. 1993 Jul 2;46(1-2):430–432. doi: 10.1016/0167-0115(93)90110-t. [DOI] [PubMed] [Google Scholar]
- Butterworth J. F., 4th, Strichartz G. R. Molecular mechanisms of local anesthesia: a review. Anesthesiology. 1990 Apr;72(4):711–734. doi: 10.1097/00000542-199004000-00022. [DOI] [PubMed] [Google Scholar]
- Caeser M., Seabrook G. R., Kemp J. A. Block of voltage-dependent sodium currents by the substance P receptor antagonist (+/-)-CP-96,345 in neurones cultured from rat cortex. Br J Pharmacol. 1993 Aug;109(4):918–924. doi: 10.1111/j.1476-5381.1993.tb13708.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Carruette A., Moussaoui S. M., Champion A., Cottez D., Goniot P., Garret C. Comparison in different tissue preparations of the in vitro pharmacological profile of RP 67580, a new non-peptide substance P antagonist. Neuropeptides. 1992 Dec;23(4):245–250. doi: 10.1016/0143-4179(92)90131-f. [DOI] [PubMed] [Google Scholar]
- Constantine J. W., Lebel W. S., Woody H. A. Inhibition of tachykinin-induced hypotension in dogs by CP-96,345, a selective blocker of NK-1 receptors. Naunyn Schmiedebergs Arch Pharmacol. 1991 Oct;344(4):471–477. doi: 10.1007/BF00172588. [DOI] [PubMed] [Google Scholar]
- Fong T. M., Cascieri M. A., Yu H., Bansal A., Swain C., Strader C. D. Amino-aromatic interaction between histidine 197 of the neurokinin-1 receptor and CP 96345. Nature. 1993 Mar 25;362(6418):350–353. doi: 10.1038/362350a0. [DOI] [PubMed] [Google Scholar]
- Fujiwara M., Hayashi H., Muramatsu I., Ueda N. Supersensitivity of the rabbit iris sphincter muscle induced by trigeminal denervation: the role of substance P. J Physiol. 1984 May;350:583–597. doi: 10.1113/jphysiol.1984.sp015219. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gamse R., Petsche U., Lembeck F., Jancsò G. Capsaicin applied to peripheral nerve inhibits axoplasmic transport of substance P and somatostatin. Brain Res. 1982 May 13;239(2):447–462. doi: 10.1016/0006-8993(82)90521-2. [DOI] [PubMed] [Google Scholar]
- Garret C., Carruette A., Fardin V., Moussaoui S., Peyronel J. F., Blanchard J. C., Laduron P. M. Pharmacological properties of a potent and selective nonpeptide substance P antagonist. Proc Natl Acad Sci U S A. 1991 Nov 15;88(22):10208–10212. doi: 10.1073/pnas.88.22.10208. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gether U., Johansen T. E., Snider R. M., Lowe J. A., 3rd, Nakanishi S., Schwartz T. W. Different binding epitopes on the NK1 receptor for substance P and non-peptide antagonist. Nature. 1993 Mar 25;362(6418):345–348. doi: 10.1038/362345a0. [DOI] [PubMed] [Google Scholar]
- Guard S., Boyle S. J., Tang K. W., Watling K. J., McKnight A. T., Woodruff G. N. The interaction of the NK1 receptor antagonist CP-96,345 with L-type calcium channels and its functional consequences. Br J Pharmacol. 1993 Sep;110(1):385–391. doi: 10.1111/j.1476-5381.1993.tb13821.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hahin R., Strichartz G. Effects of deuterium oxide on the rate and dissociation constants for saxitoxin and tetrodotoxin action. Voltage-clamp studies on frog myelinated nerve. J Gen Physiol. 1981 Aug;78(2):113–139. doi: 10.1085/jgp.78.2.113. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hall J. M., Flowers J. M., Morton I. K. A pharmacological study of NK1 and NK2 tachykinin receptor characteristics in the rat isolated urinary bladder. Br J Pharmacol. 1992 Nov;107(3):777–784. doi: 10.1111/j.1476-5381.1992.tb14523.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hall J. M., Mitchell D., Morton I. K. Neurokinin receptors in the rabbit iris sphincter characterised by novel agonist ligands. Eur J Pharmacol. 1991 Jun 18;199(1):9–14. doi: 10.1016/0014-2999(91)90630-9. [DOI] [PubMed] [Google Scholar]
- Hall J. M., Mitchell D., Morton I. K. Tachykinin receptors mediating responses to sensory nerve stimulation and exogenous tachykinins and analogues in the rabbit isolated iris sphincter. Br J Pharmacol. 1993 Aug;109(4):1008–1013. doi: 10.1111/j.1476-5381.1993.tb13721.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Håkanson R., Beding B., Ekman R., Heilig M., Wahlestedt C., Sundler F. Multiple tachykinin pools in sensory nerve fibres in the rabbit iris. Neuroscience. 1987 Jun;21(3):943–950. doi: 10.1016/0306-4522(87)90049-2. [DOI] [PubMed] [Google Scholar]
- Kao C. Y. Tetrodotoxin, saxitoxin and their significance in the study of excitation phenomena. Pharmacol Rev. 1966 Jun;18(2):997–1049. [PubMed] [Google Scholar]
- Lawrence K. B., Venepalli B. R., Appell K. C., Goswami R., Logan M. E., Tomczuk B. E., Yanni J. M. Synthesis and substance P antagonist activity of naphthimidazolium derivatives. J Med Chem. 1992 Apr 3;35(7):1273–1279. doi: 10.1021/jm00085a015. [DOI] [PubMed] [Google Scholar]
- Lecci A., Giuliani S., Patacchini R., Viti G., Maggi C. A. Role of NK1 tachykinin receptors in thermonociception: effect of (+/-)-CP 96,345, a non-peptide substance P antagonist, on the hot plate test in mice. Neurosci Lett. 1991 Aug 19;129(2):299–302. doi: 10.1016/0304-3940(91)90485-c. [DOI] [PubMed] [Google Scholar]
- Lee-Son S., Wang G. K., Concus A., Crill E., Strichartz G. Stereoselective inhibition of neuronal sodium channels by local anesthetics. Evidence for two sites of action? Anesthesiology. 1992 Aug;77(2):324–335. doi: 10.1097/00000542-199208000-00016. [DOI] [PubMed] [Google Scholar]
- Maggi C. A., Patacchini R., Rovero P., Giachetti A. Tachykinin receptors and tachykinin receptor antagonists. J Auton Pharmacol. 1993 Feb;13(1):23–93. doi: 10.1111/j.1474-8673.1993.tb00396.x. [DOI] [PubMed] [Google Scholar]
- Maggio J. E. Tachykinins. Annu Rev Neurosci. 1988;11:13–28. doi: 10.1146/annurev.ne.11.030188.000305. [DOI] [PubMed] [Google Scholar]
- Martin C. A., Naline E., Emonds-Alt X., Advenier C. Influence of (+/-)-CP-96,345 and SR 48968 on electrical field stimulation of the isolated guinea-pig main bronchus. Eur J Pharmacol. 1992 Dec 2;224(2-3):137–143. doi: 10.1016/0014-2999(92)90797-8. [DOI] [PubMed] [Google Scholar]
- Montal M. Molecular anatomy and molecular design of channel proteins. FASEB J. 1990 Jun;4(9):2623–2635. doi: 10.1096/fasebj.4.9.1693348. [DOI] [PubMed] [Google Scholar]
- Nagahisa A., Asai R., Kanai Y., Murase A., Tsuchiya-Nakagaki M., Nakagaki T., Shieh T. C., Taniguchi K. Non-specific activity of (+/-)-CP-96,345 in models of pain and inflammation. Br J Pharmacol. 1992 Oct;107(2):273–275. doi: 10.1111/j.1476-5381.1992.tb12737.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Otsuka M., Yoshioka K. Neurotransmitter functions of mammalian tachykinins. Physiol Rev. 1993 Apr;73(2):229–308. doi: 10.1152/physrev.1993.73.2.229. [DOI] [PubMed] [Google Scholar]
- Patacchini R., Santicioli P., Astolfi M., Rovero P., Viti G., Maggi C. A. Activity of peptide and non-peptide antagonists at peripheral NK1 receptors. Eur J Pharmacol. 1992 Apr 29;215(1):93–98. doi: 10.1016/0014-2999(92)90613-9. [DOI] [PubMed] [Google Scholar]
- Snider R. M., Constantine J. W., Lowe J. A., 3rd, Longo K. P., Lebel W. S., Woody H. A., Drozda S. E., Desai M. C., Vinick F. J., Spencer R. W. A potent nonpeptide antagonist of the substance P (NK1) receptor. Science. 1991 Jan 25;251(4992):435–437. doi: 10.1126/science.1703323. [DOI] [PubMed] [Google Scholar]
- Stjernquist M., Håkanson R., Leander S., Owman C., Sundler F., Uddman R. Immunohistochemical localization of substance P, vasoactive intestinal polypeptide and gastrin-releasing peptide in vas deferens and seminal vesicle, and the effect of these and eight other neuropeptides on resting tension and neurally evoked contractile activity. Regul Pept. 1983 Sep;7(1):67–86. doi: 10.1016/0167-0115(83)90282-3. [DOI] [PubMed] [Google Scholar]
- Tamura K., Mutabagani K., Wood J. D. Analysis of a nonpeptide antagonist for substance P on myenteric neurons of guinea-pig small intestine. Eur J Pharmacol. 1993 Mar 2;232(2-3):235–239. doi: 10.1016/0014-2999(93)90779-h. [DOI] [PubMed] [Google Scholar]
- Tanabe T., Takeshima H., Mikami A., Flockerzi V., Takahashi H., Kangawa K., Kojima M., Matsuo H., Hirose T., Numa S. Primary structure of the receptor for calcium channel blockers from skeletal muscle. Nature. 1987 Jul 23;328(6128):313–318. doi: 10.1038/328313a0. [DOI] [PubMed] [Google Scholar]
- Wahlestedt C., Bynke G., Beding B., von Leithner P., Håkanson R. Neurogenic mechanisms in control of the rabbit iris sphincter muscle. Eur J Pharmacol. 1985 Nov 19;117(3):303–309. doi: 10.1016/0014-2999(85)90003-2. [DOI] [PubMed] [Google Scholar]
- Wang Z. Y., Håkanson R. (+/-)-CP-96,345, a selective tachykinin NK1 receptor antagonist, has non-specific actions on neurotransmission. Br J Pharmacol. 1992 Nov;107(3):762–765. doi: 10.1111/j.1476-5381.1992.tb14520.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wang Z. Y., Håkanson R. The electrically evoked, tachykinin-mediated contractile response of the isolated rabbit iris sphincter muscle involves NK1 receptors only. Eur J Pharmacol. 1992 Jun 5;216(2):327–329. doi: 10.1016/0014-2999(92)90380-m. [DOI] [PubMed] [Google Scholar]
- Wang Z. Y., Håkanson R. The rabbit iris sphincter contains NK1 and NK3 but not NK2 receptors: a study with selective agonists and antagonists. Regul Pept. 1993 Apr 8;44(3):269–275. doi: 10.1016/0167-0115(93)90136-v. [DOI] [PubMed] [Google Scholar]
- Watling K. J. Nonpeptide antagonists herald new era in tachykinin research. Trends Pharmacol Sci. 1992 Jul;13(7):266–269. doi: 10.1016/0165-6147(92)90082-h. [DOI] [PubMed] [Google Scholar]