NK-1 receptor mediation of neurogenic plasma extravasation in rat skin
- PMID: 2477105
- PMCID: PMC1854634
- DOI: 10.1111/j.1476-5381.1989.tb12583.x
NK-1 receptor mediation of neurogenic plasma extravasation in rat skin
Abstract
1. Plasma extravasation was induced by electrical nerve stimulation and by perfusion of tachykinins over a vacuum-induced blister base on rat footpad. 2. Stimulation of the sciatic nerve (18 V, 15 Hz, 0.5 ms) for 20 min produced a significant increase in the protein content of the perfusate. The response in capsaicin pretreated rats was only 4% of the control response. This indicates that the electrically-induced plasma extravasation response was mediated by capsaicin-sensitive sensory fibres. 3. Exogenous perfusion of the mammalian tachykinins substance P, neurokinin A and neurokinin B and the non-mammalian tachykinins physalaemin, kassinin and eledoisin was used to determine the tachykinin receptor type mediating the plasma extravasation response. Dose-response curves of the tachykinins (10(-9) M-10(-4) M) gave a rank order of potency of substance P = physalaemin greater than eledoisin greater than or equal to kassinin greater than neurokinin B = neurokinin A. 4. In addition, specific agonists of neurokinin receptors were perfused. Perfusion of [Glp6, D-Pro9] SP6-11 and [Glp6, L-Pro9]SP6-11 demonstrated that the L-Pro isomer was much more potent than the D-Pro isomer. 5. The rank order of potency and the greater potency of [Glp6, L-Pro9]SP6-11 over its D-isomer indicate an NK-1 neurokinin receptor mediates plasma extravasation in rat footpad skin.
Similar articles
-
Effects of tachykinins and selective tachykinin receptor agonists on vascular permeability in the rat lower urinary tract: evidence for the involvement of NK-1 receptors.J Auton Pharmacol. 1989 Aug;9(4):253-63. doi: 10.1111/j.1474-8673.1989.tb00216.x. J Auton Pharmacol. 1989. PMID: 2475507
-
Actions of tachykinins on the rabbit mesenteric artery: substance P and [Glp6,L-Pro9]SP6-11 are potent agonists for endothelial neurokinin-1 receptors.Br J Pharmacol. 1989 Aug;97(4):1218-24. doi: 10.1111/j.1476-5381.1989.tb12581.x. Br J Pharmacol. 1989. PMID: 2477103 Free PMC article.
-
Tachykinin-induced vasodilatation in rat skin measured with a laser-Doppler flowmeter: evidence for receptor-mediated effects.Regul Pept. 1989 Jun-Jul;25(3):267-75. doi: 10.1016/0167-0115(89)90175-4. Regul Pept. 1989. PMID: 2475891
-
Substance P receptors in the nervous system and possible receptor subtypes.Ciba Found Symp. 1982;(91):186-205. doi: 10.1002/9780470720738.ch11. Ciba Found Symp. 1982. PMID: 6183070 Review.
-
Are the proposed substance P receptor sub-types, substance P receptors?Life Sci. 1984 Aug 20;35(8):797-808. doi: 10.1016/0024-3205(84)90403-x. Life Sci. 1984. PMID: 6207411 Review.
Cited by
-
Substance P and capsaicin-induced mechanical hyperalgesia in the rat knee joint; the involvement of bradykinin B1 and B2 receptors.Br J Pharmacol. 1996 Aug;118(8):2206-12. doi: 10.1111/j.1476-5381.1996.tb15664.x. Br J Pharmacol. 1996. PMID: 8864563 Free PMC article.
-
Effect of a calcitonin gene-related peptide antagonist (CGRP8-37) on skin vasodilatation and oedema induced by stimulation of the rat saphenous nerve.Br J Pharmacol. 1993 Oct;110(2):772-6. doi: 10.1111/j.1476-5381.1993.tb13878.x. Br J Pharmacol. 1993. PMID: 8242250 Free PMC article.
-
Neurobiological mechanisms of pelvic pain.Biomed Res Int. 2014;2014:903848. doi: 10.1155/2014/903848. Epub 2014 Jul 8. Biomed Res Int. 2014. PMID: 25110704 Free PMC article. Review.
-
Involvement of tachykinin receptors in oedema formation and plasma extravasation induced by substance P, neurokinin A, and neurokinin B in mouse ear.Inflamm Res. 1996 Jul;45(7):316-23. doi: 10.1007/BF02252943. Inflamm Res. 1996. PMID: 8841832
-
Inhibition of hind-paw edema and cutaneous vascular plasma extravasation by 2-chloro-3-methoxycarbonylpropionamido-1,4-naphthoquinone (PP1D1) in mice.Naunyn Schmiedebergs Arch Pharmacol. 1996 Dec;354(6):779-84. doi: 10.1007/BF00166905. Naunyn Schmiedebergs Arch Pharmacol. 1996. PMID: 8971739
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Molecular Biology Databases