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. 1981 Jun;73(2):517–523. doi: 10.1111/j.1476-5381.1981.tb10451.x

The effects of substance P and related peptides on alpha-amylase release from rat parotid gland slices.

C L Brown, M R Hanley
PMCID: PMC2071672  PMID: 6165421

Abstract

1 The effects of substance P and related peptides on amylase release from rat parotid gland slices have been investigated. 2 Supramaximal concentrations (1 microM) of substance P caused enhancement of amylase release over the basal level within 1 min; this lasted for at least 40 min at 30 degrees C. 3 Substance P-stimulated amylase release was partially dependent on extracellular calcium and could be inhibited by 50% upon removal of extracellular calcium. 4 Substance P stimulated amylase release in a dose-dependent manner with an ED50 of 18 nM. 5 All C-terminal fragments of substance P were less potent than substance P in stimulating amylase release. The C-terminal hexapeptide of substance P was the minimum structure for potent activity in this system, having 1/3 to 1/8 the potency of substance P. There was a dramatic drop in potency for the C-terminal pentapeptide of substance P or substance P free acid. Physalaemin was more potent than substance P (ED50 = 7 nM), eledoisin was about equipotent with substance P (ED50 = 17 nM), and kassinin less potent that substance P (ED50 = 150 nM). 6 The structure-activity profile observed is very similar to that for stimulation of salivation in vivo, indicating that the same receptors are involved in mediating these responses. 7 All the fragments of substance P tested were capable of eliciting a full amylase release response. This indicates that the apparent partial agonist action of the C-terminal nonapeptide fragment on in vivo salivation is not explicable at the receptor level.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Batzri S., Selinger Z. Enzyme secretion mediated by the epinephrine -receptor in rat parotid slices. Factors governing efficiency of the process. J Biol Chem. 1973 Jan 10;248(1):356–360. [PubMed] [Google Scholar]
  2. Blumberg S., Teichberg V. I. Biological activity and enzymic degradation of substance P analogs: implications for studies of the substance P receptor. Biochem Biophys Res Commun. 1979 Sep 12;90(1):347–354. doi: 10.1016/0006-291x(79)91631-0. [DOI] [PubMed] [Google Scholar]
  3. Bury R. W., Mashford M. L. Biological activity of C-terminal partial sequences of substance P. J Med Chem. 1976 Jun;19(6):854–856. doi: 10.1021/jm00228a028. [DOI] [PubMed] [Google Scholar]
  4. Butcher F. R. The role of calcium and cyclic nucleotides in alpha-amylase release from slices of rat parotid: studies with the divalent cation ionophore A-23187. Metabolism. 1975 Mar;24(3):409–418. doi: 10.1016/0026-0495(75)90120-1. [DOI] [PubMed] [Google Scholar]
  5. Chang M. M., Leeman S. E. Isolation of a sialogogic peptide from bovine hypothalamic tissue and its characterization as substance P. J Biol Chem. 1970 Sep 25;245(18):4784–4790. [PubMed] [Google Scholar]
  6. Chang M. M., Leeman S. E., Niall H. D. Amino-acid sequence of substance P. Nat New Biol. 1971 Jul 21;232(29):86–87. doi: 10.1038/newbio232086a0. [DOI] [PubMed] [Google Scholar]
  7. Erspamer G. F., Erspamer V., Piccinelli D. Parallel bioassay of physalaemin and kassinin, a tachykinin dodecapeptide from the skin of the African frog Kassina senegalensis. Naunyn Schmiedebergs Arch Pharmacol. 1980 Feb;311(1):61–65. doi: 10.1007/BF00500303. [DOI] [PubMed] [Google Scholar]
  8. Friedman Z. Y., Selinger Z. A transient release of potassium mediated by the action of substance P on rat parotid slices. J Physiol. 1978 May;278:461–469. doi: 10.1113/jphysiol.1978.sp012317. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Gallacher D. V., Petersen O. H. Substance P increases membrane conductance in parotid acinar cells. Nature. 1980 Jan 24;283(5745):393–395. doi: 10.1038/283393a0. [DOI] [PubMed] [Google Scholar]
  10. Hanley M. R., Lee C. M., Michell R. H., Jones L. M. Similar effects of substance P and related peptides on salivation and on phosphatidylinositol turnover in rat salivary glands. Mol Pharmacol. 1980 Jul;18(1):78–83. [PubMed] [Google Scholar]
  11. Jensen R. T., Gardner J. D. Interaction of physalaemin, substance P, and eledoisin with specific membrane receptors on pancreatic acinar cells. Proc Natl Acad Sci U S A. 1979 Nov;76(11):5679–5683. doi: 10.1073/pnas.76.11.5679. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Jones L. M., Michell R. H. Enhanced phosphatidylinositol breakdown as a calcium-indepepdnet response of rat parotid fragments to substance P. Biochem Soc Trans. 1978;6(5):1035–1037. doi: 10.1042/bst0061035. [DOI] [PubMed] [Google Scholar]
  13. Kanagasuntheram P., Randle P. J. Calcium metabolism and amylase release in rat parotid acinar cells. Biochem J. 1976 Dec 15;160(3):547–564. doi: 10.1042/bj1600547. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Leeman S. E., Hammerschlag R. Stimulation of salivary secretion by a factor extracted from hypothalamic tissue. Endocrinology. 1967 Oct;81(4):803–810. doi: 10.1210/endo-81-4-803. [DOI] [PubMed] [Google Scholar]
  15. Leslie B. A., Putney J. W., Jr, Sherman J. M. alpha-Adrenergic, beta-adrenergic and cholinergic mechanisms for amylase secretion by rat parotid gland in vitro. J Physiol. 1976 Sep;260(2):351–370. doi: 10.1113/jphysiol.1976.sp011519. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Liang T., Cascieri M. A. Substance P stimulation of amylase release by isolated parotid cells and inhibition of substance P induction of salivation by vasoactive peptides. Mol Cell Endocrinol. 1979 Sep;15(3):151–162. doi: 10.1016/0303-7207(79)90035-2. [DOI] [PubMed] [Google Scholar]
  17. Marier S. H., Putney J. W., Jr, Van de Walle C. M. Control of calcium channels by membrane receptors in the rat parotid gland. J Physiol. 1978 Jun;279:141–151. doi: 10.1113/jphysiol.1978.sp012336. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Putney J. W., Jr Muscarinic, alpha-adrenergic and peptide receptors regulate the same calcium influx sites in the parotid gland. J Physiol. 1977 Jun;268(1):139–149. doi: 10.1113/jphysiol.1977.sp011851. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Rudich L., Butcher F. R. Effect of substance P and eledoisin on K+ efflux, amylase release and cyclic nucleotide levels in slices of rat parotid gland. Biochim Biophys Acta. 1976 Oct 22;444(3):704–711. doi: 10.1016/0304-4165(76)90317-2. [DOI] [PubMed] [Google Scholar]
  20. Sjödin L., Brodin E., Nilsson G., Conlon T. P. Interaction of substance P with dispersed pancreatic acinar cells from the guinea pig. Binding of radioiodinated peptide. Acta Physiol Scand. 1980 May;109(1):97–105. doi: 10.1111/j.1748-1716.1980.tb06570.x. [DOI] [PubMed] [Google Scholar]
  21. Spearman T. N., Pritchard E. T. Potassium release from submandibular salivary gland in vitro. Biochim Biophys Acta. 1977 Apr 1;466(1):198–207. doi: 10.1016/0005-2736(77)90219-x. [DOI] [PubMed] [Google Scholar]
  22. V Euler U. S., Gaddum J. H. An unidentified depressor substance in certain tissue extracts. J Physiol. 1931 Jun 6;72(1):74–87. doi: 10.1113/jphysiol.1931.sp002763. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Watson E. L., Friedman J., Siegel I. A. Mediation of beta-adrenergic stimulated amylase release from mouse parotid gland. Life Sci. 1980 Jun 2;26(22):1919–1926. doi: 10.1016/0024-3205(80)90622-0. [DOI] [PubMed] [Google Scholar]

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