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PMID: 7990967 Published · ppublish English Journal Article

Effects of metal cations on [3H]alpha,beta-methylene ATP binding in rat vas deferens.

Naunyn-Schmiedeberg's archives of pharmacology ·Vol. 350 ·No. 2 ·1994-08-00 ·Pages 113-22

Michel AD, Humphrey PP

Abstract

In this study we have examined the effect of metal cations (as their chloride salts) on the binding of [3H]alpha,beta-methylene ATP ([3H]alpha beta meATP) to rat vas deferens membranes using a vacuum filtration receptor binding assay. Whereas NaCl and KCl (0.01 and 30 mM) did not affect total binding of 1 nM [3H]alpha beta meATP, several divalent and trivalent cation salts markedly increased binding. The trivalent cation salts, FeCl3 and AlCl3 (0.1 to 100 microM), produced the greatest increases in total binding of [3H]alpha beta meATP, however, their effects were most probably due to precipitation of the radioligand. In contrast, several divalent cations, at concentrations between 1 microM and 1-10 mM, increased total binding of [3H]alpha beta meATP to rat vas deferens by between 87% and 215% while having no effect on either filter binding or non specific binding. The following pEC50 values for potentiating binding of the radioligand were obtained: ZnCl2 (5.44), MnCl2 (4.52), CaCl2 (4.17), CoCl2 (4.06), MgCl2 (3.67) and BaCl2 (3.10). Both EDTA and EGTA (0.01-1 mM) inhibited the binding of the radioligand. The effects of ZnCl2, CaCl2 and MgCl2 were examined in saturation studies. In the absence of added divalent cations, [3H]alpha beta meATP labelled both high (pKd = 9.15) and low (pKd = 7.06) affinity binding sites. The affinity of the radioligand for its high affinity sites was increased by 3 mM CaCl2 (pKd = 9.56) and by 30 microM ZnCl2 (pKd = 9.46) but not by 3 mM MgCl2. The Bmax of the low affinity site for [3H]alpha beta meATP was increased (approximately 4 fold) by both 3 mM MgCl2 and 30 microM ZnCl2 but not by 3 mM CaCl2. The selective effect of CaCl2 on the high affinity binding sites enabled these sites to be labelled in the presence of 3 mM CaCl2 using a low concentration of [3H]alpha beta meATP (1 nM); the sites exhibited the binding characteristics expected of the P2x purinoceptor. The selective effect of MgCl2 on the low affinity binding sites enabled these sites to be labelled in the presence of 3 mM MgCl2 and using a high concentration of [3H]alpha beta meATP (100 nM). A comparison of the binding characteristics of the high and low affinity sites for [3H]alpha beta meATP revealed several other differences, in addition to their cation selectivity.(ABSTRACT TRUNCATED AT 400 WORDS)

MeSH Terms
Adenosine Triphosphate/analogs & derivatives,metabolism Aluminum/pharmacology Animals Binding Sites Calcium/pharmacology Chemical Precipitation Edetic Acid/pharmacology In Vitro Techniques Magnesium/pharmacology Male Rats Rats, Sprague-Dawley Tritium Vas Deferens/metabolism Zinc/pharmacology
Chemicals
Tritium Adenosine Triphosphate Edetic Acid Aluminum Magnesium Zinc alpha,beta-methyleneadenosine 5'-triphosphate Calcium
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Michel A D
Glaxo Institute of Applied Pharmacology, Department of Pharmacology, University of Cambridge, UK.
Humphrey P P
References (26)
26 references, click to expand
  1. Cloning and functional expression of a brain G-protein-coupled ATP receptor.
    FEBS Lett. 1993 Jun 14;324(2):219-25 PMID: 8508924
  2. Triphosphate, the key structure of the ATP molecule responsible for interaction with P2X-purinoceptors.
    Gen Pharmacol. 1993 May;24(3):637-40 PMID: 8365644
  3. Electron spin resonance of ferromagnetic particles in airborne dust.
    Nature. 1968 May 4;218(5140):497-8 PMID: 4296987
  4. Biochemical properties of a P2Y-purinergic receptor.
    Ann N Y Acad Sci. 1990;603:256-66 PMID: 2291525
  5. Cationic channels activated by extracellular ATP in rat sensory neurons.
    Neuroscience. 1988 Dec;27(3):995-1000 PMID: 2855265
  6. Effects of adenyl nucleotides and carbachol on cooperative interactions among G proteins.
    Biochemistry. 1992 Nov 10;31(44):10908-21 PMID: 1420202
  7. High- and low-affinity binding sites for [3H]-alpha, beta-methylene ATP in rat urinary bladder membranes.
    Br J Pharmacol. 1990 Oct;101(2):291-6 PMID: 2257437
  8. Guanine nucleotide-sensitive interaction of a radiolabeled agonist with a phospholipase C-linked P2y-purinergic receptor.
    J Biol Chem. 1989 Apr 15;264(11):6202-6 PMID: 2495280
  9. Signal transduction by P2-purinergic receptors for extracellular ATP.
    Am J Respir Cell Mol Biol. 1991 Apr;4(4):295-300 PMID: 1707633
  10. Desensitization of the nicotinic acetylcholine receptor: molecular mechanisms and effect of modulators.
    Cell Mol Neurobiol. 1989 Jun;9(2):141-78 PMID: 2663167
  11. Low calcium and calcium antagonists potentiate the contraction of guinea-pig vas deferens induced by ATP: a permissive role for P2-purinoceptors.
    Eur J Pharmacol. 1989 May 30;164(3):507-13 PMID: 2767121
  12. Calcium buffer solutions and how to make them: a do it yourself guide.
    Can J Physiol Pharmacol. 1991 Nov;69(11):1733-49 PMID: 1804518
  13. Distribution and characterisation of [3H]alpha,beta-methylene ATP binding sites in the rat.
    Naunyn Schmiedebergs Arch Pharmacol. 1993 Dec;348(6):608-17 PMID: 8133903
  14. Comparison of contractions of the smooth muscle of the guinea-pig vas deferens induced by ATP and related nucleotides.
    Eur J Pharmacol. 1982 Jul 9;81(2):193-204 PMID: 7117373
  15. Relationship between the inhibition constant (K1) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction.
    Biochem Pharmacol. 1973 Dec 1;22(23):3099-108 PMID: 4202581
  16. Evidence that the P2x purinoceptor of the smooth muscle of the guinea pig vas deferens is an ATP4- receptor.
    J Pharmacol Exp Ther. 1990 Oct;255(1):46-51 PMID: 2213570
  17. Solubilization and molecular size determination of the P2x purinoceptor from rat vas deferens.
    J Biol Chem. 1992 Sep 5;267(25):17581-7 PMID: 1387637
  18. Ligand: a versatile computerized approach for characterization of ligand-binding systems.
    Anal Biochem. 1980 Sep 1;107(1):220-39 PMID: 6254391
  19. Pharmacology and electrophysiology of ATP-activated ion channels.
    Trends Pharmacol Sci. 1992 Mar;13(3):87-90 PMID: 1374198
  20. ATP-activated channels in rat and bullfrog sensory neurons: concentration dependence and kinetics.
    J Neurosci. 1990 Jan;10(1):1-10 PMID: 1688928
  21. Is there a basis for distinguishing two types of P2-purinoceptor?
    Gen Pharmacol. 1985;16(5):433-40 PMID: 2996968
  22. Atropine resistant excitation of the urinary bladder: the possibility of transmission via nerves releasing a purine nucleotide.
    Br J Pharmacol. 1972 Mar;44(3):451-61 PMID: 4339250
  23. Zn2+ potentiates ATP-activated currents in rat sympathetic neurons.
    Pflugers Arch. 1993 Jul;424(2):152-8 PMID: 7692385
  24. Zn2+ potentiates excitatory action of ATP on mammalian neurons.
    Proc Natl Acad Sci U S A. 1993 Sep 1;90(17):8264-7 PMID: 7690146
  25. Expression cloning of an ATP receptor from mouse neuroblastoma cells.
    Proc Natl Acad Sci U S A. 1993 Jun 1;90(11):5113-7 PMID: 7685114
  26. Overview. Purinergic mechanisms.
    Ann N Y Acad Sci. 1990;603:1-17; discussion 18 PMID: 1981306
Article Info
Journal
Naunyn-Schmiedeberg's archives of pharmacology
Abbr.
Naunyn Schmiedebergs Arch Pharmacol
ISSN
0028-1298
Published
1994-08-00
Pages
113-22
Language
English
Region
Germany
NLM ID
0326264
Subset
IM
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