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. 1974 May;140(2):135–142. doi: 10.1042/bj1400135

The effect of nickel on secretory systems. Studies on the release of amylase, insulin and growth hormone

Robert L Dormer 1, Alan L Kerbey 1, Margaret McPherson 1, Susan Manley 1, Stephen J H Ashcroft 1, J George Schofield 1, Philip J Randle 1
PMCID: PMC1167985  PMID: 4375956

Abstract

The effects of Ni2+ on the release of amylase from rat parotids, insulin from mouse pancreatic islets and growth hormone from bovine pituitary slices were investigated. In all these secretory systems, Ni2+ was shown to inhibit release evoked by a variety of stimuli both physiological and pharmacological. Measurements of rates of substrate oxidation and tissue concentrations of ATP and 3′:5′-cyclic AMP suggest that this inhibitory action of Ni2+ does not arise through an effect on energy metabolism or cyclic AMP metabolism. It is concluded that although some effects of Ni2+ may involve antagonism between Ni2+ and Ca2+ in stimulus–secretion coupling, others appear to be independent of Ca2+. It is suggested that Ni2+ may block exocytosis by interfering with either secretory-granule migration or membrane fusion and microvillus formation. The possible mode of action of Ni2+ and its potential use as a tool in the study of exocytosis are discussed.

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Selected References

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

  1. Amsterdam A., Ohad I., Schramm M. Dynamic changes in the ultrastructure of the acinar cell of the rat parotid gland during the secretory cycle. J Cell Biol. 1969 Jun;41(3):753–773. doi: 10.1083/jcb.41.3.753. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Ashcroft S. J., Weerasinghe L. C., Randle P. J. Interrelationship of islet metabolism, adenosine triphosphate content and insulin release. Biochem J. 1973 Feb;132(2):223–231. doi: 10.1042/bj1320223. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Babad H., Ben-Zvi R., Bdolah A., Schramm M. The mechanism of enzyme secretion by the cell. 4. Effects of inducers, substrates and inhibitors on amylase secretion by rat parotid slices. Eur J Biochem. 1967 Mar;1(1):96–101. doi: 10.1111/j.1432-1033.1967.tb00049.x. [DOI] [PubMed] [Google Scholar]
  4. Benoit P. R., Mambrini J. Modification of transmitter release by ions which prolong the presynaptic action potential. J Physiol. 1970 Oct;210(3):681–695. doi: 10.1113/jphysiol.1970.sp009235. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Coll-Garcia E., Gill J. R. Insulin release by isolated pancreatic islets of the mouse incubated in vitro. Diabetologia. 1969 Apr;5(2):61–66. doi: 10.1007/BF01211999. [DOI] [PubMed] [Google Scholar]
  6. Cooper R. H., Ashcroft S. J., Randle P. J. Concentration of adenosine 3':5'-cyclic monophosphate in mouse pancreatic islets measured by a protein-binding radioassay. Biochem J. 1973 Jun;134(2):599–605. doi: 10.1042/bj1340599. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Cooper R. H., McPherson M., Schofield J. G. The effect of prostaglandins on ox pituitary content of adenosine 3':5'-cyclic monophosphate and the release of growth hormone. Biochem J. 1972 Mar;127(1):143–154. doi: 10.1042/bj1270143. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Douglas W. W. Stimulus-secretion coupling: the concept and clues from chromaffin and other cells. Br J Pharmacol. 1968 Nov;34(3):451–474. doi: 10.1111/j.1476-5381.1968.tb08474.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. FARQUHAR M. G. Origin and fate of secretory granules in cells of the anterior pituitary gland. Trans N Y Acad Sci. 1961 Feb;23:346–351. doi: 10.1111/j.2164-0947.1961.tb01361.x. [DOI] [PubMed] [Google Scholar]
  10. KAUFMANN R., FLECKENSTEIN A. CA++-KOMPETITIVE ELEKTRO-MECHANISCHE ENTKOPPELUNG DURCH NI++- UND CO++-IONEN AM WARMBLUETERMYODARD. Pflugers Arch Gesamte Physiol Menschen Tiere. 1965;282:290–297. [PubMed] [Google Scholar]
  11. Kleinfeld M., Stein E. Action of divalent cations on membrane potentials and contractility in rat atrium. Am J Physiol. 1968 Sep;215(3):593–599. doi: 10.1152/ajplegacy.1968.215.3.593. [DOI] [PubMed] [Google Scholar]
  12. LACY P. E. Electron microscopy of the beta cell of the pancreas. Am J Med. 1961 Dec;31:851–859. doi: 10.1016/0002-9343(61)90024-9. [DOI] [PubMed] [Google Scholar]
  13. LaBella F., Dular R., Vivian S., Queen G. Pituitary hormone releasing or inhibiting activity of metal ions present in hypothalamic extracts. Biochem Biophys Res Commun. 1973 Jun 8;52(3):786–791. doi: 10.1016/0006-291x(73)91006-1. [DOI] [PubMed] [Google Scholar]
  14. Malamud D. Amylase secretion from mouse parotid and pancreas: role of cyclic AMP and isoproterenol. Biochim Biophys Acta. 1972 Sep 15;279(2):373–376. doi: 10.1016/0304-4165(72)90155-9. [DOI] [PubMed] [Google Scholar]
  15. McPherson M. A., Schofield J. G. Cytochalasin B, pituitary metabolism, and the release of ox growth hormone in vitro. FEBS Lett. 1972 Jul 15;24(1):45–48. doi: 10.1016/0014-5793(72)80822-6. [DOI] [PubMed] [Google Scholar]
  16. Meiri U., Rahamimoff R. Neuromuscular transmission: inhibition by manganese ions. Science. 1972 Apr 21;176(4032):308–309. doi: 10.1126/science.176.4032.308. [DOI] [PubMed] [Google Scholar]
  17. Milner R. D., Hales C. N. Cations and the secretion of insulin. Biochim Biophys Acta. 1968 Jan 3;150(1):165–167. doi: 10.1016/0005-2736(68)90022-9. [DOI] [PubMed] [Google Scholar]
  18. Montague W., Cook J. R. The role of adenosine 3':5'-cyclic monophosphate in the regulation of insulin release by isolated rat islets of Langerhans. Biochem J. 1971 Mar;122(1):115–120. doi: 10.1042/bj1220115. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Robberecht P., Christophe J. Secretion of hydrolases by perfused fragments of rat pancreas: effect of calcium. Am J Physiol. 1971 Apr;220(4):911–917. doi: 10.1152/ajplegacy.1971.220.4.911. [DOI] [PubMed] [Google Scholar]
  20. Schofield J. G. Effect of sulphydryl reagents on the release of ox growth hormone in vitro. Biochim Biophys Acta. 1971 Dec 21;252(3):516–525. doi: 10.1016/0304-4165(71)90154-1. [DOI] [PubMed] [Google Scholar]
  21. Schofield J. G. Measurement of growth hormone released by ox anterior-pituitary slices in vitro. Biochem J. 1967 May;103(2):331–341. doi: 10.1042/bj1030331. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Schofield J. G., Stead Margaret. ATP, calcium uptake and growth hormone release. FEBS Lett. 1971 Mar 5;13(3):149–151. doi: 10.1016/0014-5793(71)80222-3. [DOI] [PubMed] [Google Scholar]
  23. Selinger Z., Naim E. The effect of calcium on amylase secretion by rat parotid slices. Biochim Biophys Acta. 1970 Apr 21;203(2):335–337. doi: 10.1016/0005-2736(70)90148-3. [DOI] [PubMed] [Google Scholar]

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