Literature DB >> 1380375

Differences in neurokinin receptor pharmacology between rat and guinea-pig superior cervical ganglia.

G R Seabrook1, M Main, B Bowery, N Wood, R G Hill.   

Abstract

1. The depolarizations elicited by seven neurokinin receptor agonists were examined in both rat and guinea-pig superior cervical ganglia by use of grease-gap methodology in the presence of tetrodotoxin (0.1 microM). Responses were normalised with respect to 1 microM eledoisin. 2. The rank order of agonist potency in the rat ganglia was senktide greater than substance P greater than substance P methyl ester = eleidosin = Sar-Met-substance P greater than neurokinin B greater than neurokinin A, whereas in guinea-pig superior cervical ganglion (SCG) the rank order was senktide greater than Sar-Met-substance P greater than neurokinin B = eledoisin = substance P methyl ester. The concentration-effect curves for substance P and neurokinin A in guinea-pig ganglia were biphasic which precluded the determination of meaningful potency values. 3. The maximal depolarization achieved by subtype selective ligands was different between these two species. On rat and guinea-pig SCG, the NK3-selective ligand, senktide, produced a maximal depolarization of 27% and 274% respectively, whereas the NK1-selective ligand, substance P methyl ester, produced depolarizations of 77% and 64% respectively. 4. The depolarizations induced by substance P methyl ester and senktide in either species were unaffected by atropine (1 microM), suggesting a lack of involvement of presynaptic neurokinin receptors in the generation of the response. 5. The potency of substance P methyl ester, senktide, and neurokinin A were unaffected by pretreating ganglia with the peptidase inhibitors bacitracin (40 micrograms ml-1), leupeptin (4 micrograms ml-1), and chymostatin (2 micrograms ml-1). Similarly, these peptidase inhibitors had no effect on the maximal depolarizations achieved by any of these agonists.6. It is evident that rat and guinea-pig superior cervical ganglia possess both NK, and NK3 receptors, but that their net contribution to depolarizations are different between the two species. The depolarizations in guinea-pig SCG are mediated predominantly by an NK3 subtype and in rat SCG by an NK, receptor subtype.

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Year:  1992        PMID: 1380375      PMCID: PMC1908729          DOI: 10.1111/j.1476-5381.1992.tb09079.x

Source DB:  PubMed          Journal:  Br J Pharmacol        ISSN: 0007-1188            Impact factor:   8.739


  22 in total

1.  Pertussis toxin-insensitive G protein mediates substance P-induced inhibition of potassium channels in brain neurons.

Authors:  Y Nakajima; S Nakajima; M Inoue
Journal:  Proc Natl Acad Sci U S A       Date:  1988-05       Impact factor: 11.205

2.  Isolation of a sialogogic peptide from bovine hypothalamic tissue and its characterization as substance P.

Authors:  M M Chang; S E Leeman
Journal:  J Biol Chem       Date:  1970-09-25       Impact factor: 5.157

3.  Substance P-containing primary sensory neurons projecting to the inferior mesenteric ganglion: evidence from combined retrograde tracing and immunohistochemistry.

Authors:  C J Dalsgaard; T Hökfelt; L G Elfvin; L Skirboll; P Emson
Journal:  Neuroscience       Date:  1982-03       Impact factor: 3.590

4.  Substance P raises neuronal membrane excitability by reducing inward rectification.

Authors:  P R Stanfield; Y Nakajima; K Yamaguchi
Journal:  Nature       Date:  1985 Jun 6-12       Impact factor: 49.962

5.  Characterization of NK-3 binding sites in rat and guinea pig cortical membranes by the selective ligand [3H]Senktide.

Authors:  A R Renzetti; P Barsacchi; M Criscuoli; A Lucacchini
Journal:  Neuropeptides       Date:  1991-03       Impact factor: 3.286

6.  On the occurrence of substance P-containing fibers in sympathetic ganglia: immunohistochemical evidence.

Authors:  T Hökfelt; L G Elfvin; M Schultzberg; M Goldstein; G Nilsson
Journal:  Brain Res       Date:  1977-08-19       Impact factor: 3.252

7.  The possible existence of multiple receptors for substance P.

Authors:  C M Lee; L L Iversen; M R Hanley; B E Sandberg
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1982-03       Impact factor: 3.000

8.  Agonist effects of [D-Pro2,D-Phe7,D-Trp9]substance P--evidence for different receptors.

Authors:  A B Hawcock; A G Hayes; M B Tyers
Journal:  Eur J Pharmacol       Date:  1982-05-07       Impact factor: 4.432

9.  Substance P: ionic basis for depolarizing responses of mouse spinal cord neurons in cell culture.

Authors:  L M Nowak; R L Macdonald
Journal:  J Neurosci       Date:  1982-08       Impact factor: 6.167

10.  Highly selective agonists for substance P receptor subtypes.

Authors:  U Wormser; R Laufer; Y Hart; M Chorev; C Gilon; Z Selinger
Journal:  EMBO J       Date:  1986-11       Impact factor: 11.598

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  3 in total

1.  Tachykinins as mediators of slow EPSPs in guinea-pig gall-bladder ganglia: involvement of neurokinin-3 receptors.

Authors:  G M Mawe
Journal:  J Physiol       Date:  1995-06-01       Impact factor: 5.182

2.  Electrophysiological effects of tachykinins and capsaicin on guinea-pig bronchial parasympathetic ganglion neurones.

Authors:  A C Myers; B J Undem
Journal:  J Physiol       Date:  1993-10       Impact factor: 5.182

3.  Bradykinin receptors in mouse and rat isolated superior cervical ganglia.

Authors:  G R Seabrook; B J Bowery; R G Hill
Journal:  Br J Pharmacol       Date:  1995-05       Impact factor: 8.739

  3 in total

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