Literature DB >> 2824947

Characterization of neurokinin receptors in various isolated organs by the use of selective agonists.

S Dion1, P D'Orléans-Juste, G Drapeau, N E Rhaleb, N Rouissi, C Tousignant, D Regoli.   

Abstract

The three mammalian neurokinins, substance P, neurokinin A and neurokinin B, as well as some agonists selective for their respective receptors, NK-P, NK-A and NK-B, were tested in a variety of pharmacological preparations in order to evaluate if the biological responses of the various tissues were mediated by single or multiple receptor types. Previous observations that the dog carotid artery, the rabbit pulmonary artery and the rat portal vein are selective preparations respectively for SP, NKA and NKB were confirmed in the present study by showing that only the respective selective agonists were active on these tissues. Multiple functional sites were demonstrated in intestinal tissues (guinea pig ileum, rat duodenum), which apparently contain the three neurokinin receptors. A large number of NK-P, together with some NK-A receptor sites were found in the guinea pig and rat urinary bladder. Similarly, the guinea pig trachea and the rabbit mesenteric vein contain NK-A and NK-P functional sites. Rat and rabbit vas deferens stimulated electrically respond as typical NK-A preparations, since they are almost insensitive to SP or NKB selective agonists. A mixture of NK-A and NK-B receptor sites has been shown to be present in the hamster urinary bladder: dog and human urinary bladder definitely contain NK-A receptors and the dog bladder also some NK-P functional sites.

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Year:  1987        PMID: 2824947     DOI: 10.1016/0024-3205(87)90538-8

Source DB:  PubMed          Journal:  Life Sci        ISSN: 0024-3205            Impact factor:   5.037


  22 in total

1.  Tachykinin-induced contraction of the guinea-pig isolated oesophageal mucosa is mediated by NK(2) receptors.

Authors:  K P Kerr; B Thai; I M Coupar
Journal:  Br J Pharmacol       Date:  2000-12       Impact factor: 8.739

2.  NK1 receptors mediate tachykinin-induced plasma extravasation in the rat knee joint.

Authors:  Y Hirayama; R Yasumitsu; A Kawamura; T Fujii
Journal:  Agents Actions       Date:  1993-11

3.  Further evidence for the existence of NK2 tachykinin receptor subtypes.

Authors:  R Patacchini; M Astolfi; L Quartara; P Rovero; A Giachetti; C A Maggi
Journal:  Br J Pharmacol       Date:  1991-09       Impact factor: 8.739

4.  Tachykinin receptors mediate atropine-resistant rat duodenal reflex contractions in vivo.

Authors:  S Giuliani; M Tramontana; A Lecci; C A Maggi
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1996 Aug-Sep       Impact factor: 3.000

5.  Spinal action of neurokinins producing cardiovascular responses in the conscious freely moving rat: evidence for a NK-1 receptor mechanism.

Authors:  H Hasséssian; G Drapeau; R Couture
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1988-12       Impact factor: 3.000

6.  Protein kinase C may regulate the tonic component of intestinal smooth muscle contraction in response to substance P.

Authors:  P Holzer; I T Lippe
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1989 Jan-Feb       Impact factor: 3.000

7.  Capillary permeability induced by intravenous neurokinins. Receptor characterization and mechanism of action.

Authors:  L Jacques; R Couture; G Drapeau; D Regoli
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1989-08       Impact factor: 3.000

8.  Neurokinin A-induced contraction of guinea-pig isolated trachea: potentiation by hepoxilins.

Authors:  O Laneuville; R Couture; C R Pace-Asciak
Journal:  Br J Pharmacol       Date:  1992-11       Impact factor: 8.739

9.  Tachykinin receptors in the guinea-pig renal pelvis: activation by exogenous and endogenous tachykinins.

Authors:  C A Maggi; R Patacchini; A Eglezos; L Quartara; S Giuliani; A Giachetti
Journal:  Br J Pharmacol       Date:  1992-09       Impact factor: 8.739

10.  FR 113680: a novel tripeptide substance P antagonist with NK1 receptor selectivity.

Authors:  H Morimoto; M Murai; Y Maeda; D Hagiwara; H Miyake; M Matsuo; T Fujii
Journal:  Br J Pharmacol       Date:  1992-05       Impact factor: 8.739

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