Skip to main content
British Journal of Pharmacology logoLink to British Journal of Pharmacology
. 1995 Feb;114(3):632–639. doi: 10.1111/j.1476-5381.1995.tb17186.x

Effects of divalent cations and La3+ on contractility and ecto-ATPase activity in the guinea-pig urinary bladder.

A U Ziganshin 1, L E Ziganshina 1, C H Hoyle 1, G Burnstock 1
PMCID: PMC1510013  PMID: 7735690

Abstract

1. Several cations (Ba2+, Cd2+, Co2+, Cu2+, Mn2+, Ni2+, Zn2+ and La3+, all as chloride salts, 1-1000 microM) were tested in the guinea-pig urinary bladder for their ability to: (i) modify contractile responses to electrical field stimulation (EFS), ATP, alpha,beta-methylene ATP (alpha,beta-meATP), carbachol (CCh), and KCl; (ii) affect ecto-ATPase activity. 2. Ba2+ (10-1000 microM) concentration-dependently potentiated contractile responses evoked by EFS (4-16 Hz), ATP (100 microM), alpha,beta-meATP (1 microM), CCh (0.5 microM), and KCl (30 mM). Ni2+ at concentrations of 1-100 microM also potentiated contractility of the urinary bladder, but at concentrations tested its effect was not concentration-dependent. Cu2+ at a concentration of 10 microM and Cd2+ at a concentration of 1 microM potentiated responses to all stimuli, except KCl. Ni2+ at a concentration of 1000 microM and Cd2+ at a concentration of 100 microM inhibited contractions evoked by all stimuli, and at a concentration of 1000 microM Cd2+ abolished any contractions. Responses to ATP and alpha,beta-meATP were selectively inhibited by Cu2+, Zn2+ or La3+, each at a concentration of 1 mM. 3. Cu2+, Ni2+, Zn2+ and La3+ (100-1000 microM) concentration-dependently inhibited ecto-ATPase activity in the urinary bladder smooth muscle preparations, while Ba2+ and Mn2+ were without effect, and Cd2+ and Co2+ caused significant inhibition only at a concentration of 1000 microM. 4. There was no correlation between the extent of ecto-ATPase inhibition and the effect on contractile activity of any of the cations.(ABSTRACT TRUNCATED AT 250 WORDS)

Full text

PDF
632

Selected References

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

  1. Adeagbo A. S., Triggle C. R. Effects of some inorganic divalent cations and protein kinase C inhibitors on endothelium-dependent relaxation in rat isolated aorta and mesenteric arteries. J Cardiovasc Pharmacol. 1991 Oct;18(4):511–521. doi: 10.1097/00005344-199110000-00006. [DOI] [PubMed] [Google Scholar]
  2. Bailey S. J., Hourani S. M. Differential effects of suramin on P2-purinoceptors mediating contraction of the guinea-pig vas deferens and urinary bladder. Br J Pharmacol. 1994 May;112(1):219–225. doi: 10.1111/j.1476-5381.1994.tb13055.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Chao S. H., Suzuki Y., Zysk J. R., Cheung W. Y. Activation of calmodulin by various metal cations as a function of ionic radius. Mol Pharmacol. 1984 Jul;26(1):75–82. [PubMed] [Google Scholar]
  4. Cox J. L., Harrison S. D., Jr Correlation of metal toxicity with in vitro calmodulin inhibition. Biochem Biophys Res Commun. 1983 Aug 30;115(1):106–111. doi: 10.1016/0006-291x(83)90975-0. [DOI] [PubMed] [Google Scholar]
  5. Culić O., Sabolić I., Zanić-Grubisić T. The stepwise hydrolysis of adenine nucleotides by ectoenzymes of rat renal brush-border membranes. Biochim Biophys Acta. 1990 Nov 30;1030(1):143–151. doi: 10.1016/0005-2736(90)90249-n. [DOI] [PubMed] [Google Scholar]
  6. Deth R., Lynch C. Inhibition of alpha-receptor-induced Ca2+ release and Ca2+ influx by Mn2+ and La3+. Eur J Pharmacol. 1981 Apr 24;71(1):1–11. doi: 10.1016/0014-2999(81)90381-2. [DOI] [PubMed] [Google Scholar]
  7. Dhalla N. S., Zhao D. Cell membrane Ca2+/Mg2+ ATPase. Prog Biophys Mol Biol. 1988;52(1):1–37. doi: 10.1016/0079-6107(88)90006-5. [DOI] [PubMed] [Google Scholar]
  8. Dombrowski K. E., Trevillyan J. M., Cone J. C., Lu Y., Phillips C. A. Identification and partial characterization of an ectoATPase expressed by human natural killer cells. Biochemistry. 1993 Jul 6;32(26):6515–6522. doi: 10.1021/bi00077a004. [DOI] [PubMed] [Google Scholar]
  9. Edwards C. The selectivity of ion channels in nerve and muscle. Neuroscience. 1982 Jun;7(6):1335–1366. doi: 10.1016/0306-4522(82)90249-4. [DOI] [PubMed] [Google Scholar]
  10. Grondal E. J., Zimmermann H. Ectonucleotidase activities associated with cholinergic synaptosomes isolated from Torpedo electric organ. J Neurochem. 1986 Sep;47(3):871–881. doi: 10.1111/j.1471-4159.1986.tb00692.x. [DOI] [PubMed] [Google Scholar]
  11. Harrow J. A., Das P. K., Dhalla N. S. Influence of some divalent cations on heart sarcolemmal bound enzymes and calcium binding. Biochem Pharmacol. 1978;27(22):2605–2609. doi: 10.1016/0006-2952(78)90334-9. [DOI] [PubMed] [Google Scholar]
  12. Hilden S. A., Madias N. E. Stimulation of canine kidney BBMV ATPase activity by acidic pH in the presence of Zn2+: an ATPase activity distinct from transport ATPases and alkaline phosphatase that may be an ecto-ATPase. Membr Biochem. 1990 Jan-Mar;9(1):69–81. doi: 10.3109/09687689009026824. [DOI] [PubMed] [Google Scholar]
  13. Hourani S. M., Chown J. A. The effects of some possible inhibitors of ectonucleotidases on the breakdown and pharmacological effects of ATP in the guinea-pig urinary bladder. Gen Pharmacol. 1989;20(4):413–416. doi: 10.1016/0306-3623(89)90188-2. [DOI] [PubMed] [Google Scholar]
  14. Huddart H., Butler D. J. Field stimulation responses of rat urinary bladder detrusor smooth-muscle. Dependence upon slow calcium channel activity determined by K+ depolarization and calcium antagonists. Gen Pharmacol. 1986;17(6):695–703. doi: 10.1016/0306-3623(86)90302-2. [DOI] [PubMed] [Google Scholar]
  15. Kreye V. A., Hofmann F., Mühleisen M. Barium can replace calcium in calmodulin-dependent contractions of skinned renal arteries of the rabbit. Pflugers Arch. 1986 Mar;406(3):308–311. doi: 10.1007/BF00640919. [DOI] [PubMed] [Google Scholar]
  16. Kurihara K., Hosoi K., Ueha T. Characterization of ecto-nucleoside triphosphatase on A-431 human epidermoidal carcinoma cells. Enzyme. 1992;46(4-5):213–220. doi: 10.1159/000468790. [DOI] [PubMed] [Google Scholar]
  17. Lawson K., Cavero I. Contractile responses to calcium chloride in rat aortic rings bathed in K+-free solution are resistant to organic calcium antagonists. Br J Pharmacol. 1989 Jan;96(1):17–22. doi: 10.1111/j.1476-5381.1989.tb11778.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Majumder G. C. Enzymic characteristics of ecto-adenosine triphosphatase in rat epididymal intact spermatozoa. Biochem J. 1981 Apr 1;195(1):103–110. doi: 10.1042/bj1950103. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Manery J. F., Dryden E. E., Still J. S., Madapallimattam G. Characteristics of skeletal muscle ecto-ATPase in situ. Can J Biochem Cell Biol. 1984 Oct;62(10):1015–1026. doi: 10.1139/o84-130. [DOI] [PubMed] [Google Scholar]
  20. Ravindran A., Schild L., Moczydlowski E. Divalent cation selectivity for external block of voltage-dependent Na+ channels prolonged by batrachotoxin. Zn2+ induces discrete substates in cardiac Na+ channels. J Gen Physiol. 1991 Jan;97(1):89–115. doi: 10.1085/jgp.97.1.89. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Rüegg U. T., Wallnöfer A., Weir S., Cauvin C. Receptor-operated calcium-permeable channels in vascular smooth muscle. J Cardiovasc Pharmacol. 1989;14 (Suppl 6):S49–S58. [PubMed] [Google Scholar]
  22. Satoh S., Kubota Y., Itoh T., Kuriyama H. Mechanisms of the Ba2+-induced contraction in smooth muscle cells of the rabbit mesenteric artery. J Gen Physiol. 1987 Feb;89(2):215–237. doi: 10.1085/jgp.89.2.215. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Sheets M. F., Hanck D. A. Mechanisms of extracellular divalent and trivalent cation block of the sodium current in canine cardiac Purkinje cells. J Physiol. 1992 Aug;454:299–320. doi: 10.1113/jphysiol.1992.sp019265. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Smolen J. E., Weissmann G. Mg2+-ATPase as a membrane ecto-enzyme of human granulocytes. Inhibitors, activators and response to phagocytosis. Biochim Biophys Acta. 1978 Oct 4;512(3):525–538. doi: 10.1016/0005-2736(78)90162-1. [DOI] [PubMed] [Google Scholar]
  25. Tuana B. S., Dhalla N. S. Purification and characterization of a Ca2+/Mg2+ ecto-ATPase from rat heart sarcolemma. Mol Cell Biochem. 1988 May;81(1):75–88. doi: 10.1007/BF00225655. [DOI] [PubMed] [Google Scholar]
  26. Van Breemen C., McNaughton E. The separation of cell membrane calcium transport from extracellular calcium exchange in vascular smooth muscle. Biochem Biophys Res Commun. 1970 May 22;39(4):567–574. doi: 10.1016/0006-291x(70)90241-x. [DOI] [PubMed] [Google Scholar]
  27. Wallnöfer A., Cauvin C., Lategan T. W., Rüegg U. T. Differential blockade of agonist- and depolarization-induced 45Ca2+ influx in smooth muscle cells. Am J Physiol. 1989 Oct;257(4 Pt 1):C607–C611. doi: 10.1152/ajpcell.1989.257.4.C607. [DOI] [PubMed] [Google Scholar]
  28. Weiss G. B., Goodman F. R. Effects of lanthanum on contraction, calcium distribution and Ca45 movements in intestinal smooth muscle. J Pharmacol Exp Ther. 1969 Sep;169(1):46–55. [PubMed] [Google Scholar]
  29. Welford L. A., Cusack N. J., Hourani S. M. ATP analogues and the guinea-pig taenia coli: a comparison of the structure-activity relationships of ectonucleotidases with those of the P2-purinoceptor. Eur J Pharmacol. 1986 Oct 7;129(3):217–224. doi: 10.1016/0014-2999(86)90431-0. [DOI] [PubMed] [Google Scholar]
  30. Welford L. A., Cusack N. J., Hourani S. M. The structure-activity relationships of ectonucleotidases and of excitatory P2-purinoceptors: evidence that dephosphorylation of ATP analogues reduces pharmacological potency. Eur J Pharmacol. 1987 Sep 2;141(1):123–130. doi: 10.1016/0014-2999(87)90418-3. [DOI] [PubMed] [Google Scholar]

Articles from British Journal of Pharmacology are provided here courtesy of The British Pharmacological Society

RESOURCES