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PMID: 6257896 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Quinacrine (mepacrine) action at frog end-plate.

The Journal of physiology ·Vol. 306 ·1980-09-00 ·Pages 261-81

Adams PR, Feltz A

Abstract

1. The effects of quinacrine on end-plate currents (e.p.c.s.), miniature end-plate currents (m.e.p.c.s.) and ionophoretic responses at voltage clamped frog end-plates were investigated. 2. A quinacrine concentration (2 microM) that by itself has little effect on m.p.e.c.s. will considerably attenuate responses to bath applied carbachol. The combined effect of the two drugs causes the m.e.p.c.s. to disappear. 3. The depressant effect of quinacrine on ionophoretic responses to carbachol or acetylcholine is increased in acid solutions and decreased in alkaline solutions, suggesting that quinacrine is active as an acridinium ion. 4. Quinacrine (2-10 microM) causes a use-dependent block of end-plate channels which manifests as an inhibitory effect of an ionophoretic prepulse on the response to a test pulse. The inhibitory interaction decays exponentially with a time constant tau s that depends on the nature of the agonist used for the prepulse, on the quinacrine concentration, and on the membrane potential. 5. Quinacrine (5-20 microM) reduces the amplitude of e.p.c.s. and m.e.p.c.s. It also increases the rate of decay of the e.p.c. or m.e.p.c. tails, which remain exponential. The decay rate constant 1/tau f increases linearly with quinacrine concentration both in the presence and absence of 3 microM-neostigmine. The slope of this linear relation increases slightly with membrane hyperpolarization. 6. These data suggest that quinacrine's main action is a slow, voltage dependent blockade of open end-plate channels, though there are probably additional effects on acetylcholinesterase and channel opening. In accordance with the open channel blocking model, 1/tau s and 1/tau f both increase linearly with quinacrine concentration. However, the slopes of these lines lead to rather different estimates of the forward blocking rate constant (8 X 10(7) and 4 X 10(8) M-1 S-1 respectively). 7. The unblocking rate constant is about 5 S-1 at -80 mV. It is much more voltage dependent than the forward rate constant.

MeSH Terms
Acetylcholine/physiology Animals Hydrogen-Ion Concentration In Vitro Techniques Ion Channels/drug effects Kinetics Membrane Potentials/drug effects Motor Endplate/drug effects,physiology Muscles/physiology Neuromuscular Junction/drug effects Quinacrine/pharmacology Rana esculenta Rana pipiens
Chemicals
Ion Channels Quinacrine Acetylcholine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Adams P R
Feltz A
References (43)
43 references, click to expand
  1. Voltage jump analysis of procaine action at frog end-plate.
    J Physiol. 1977 Jun;268(2):291-318 PMID: 301570
  2. Studies on the mechanism of action of acetylcholine antagonists on rat parasympathetic ganglion cells.
    J Physiol. 1979 Oct;295:139-70 PMID: 42780
  3. Extrinsic and intrinsic acetylcholine and barbiturate effects on frog skeletal muscle.
    Br J Pharmacol. 1970 Nov;40(3):552P-553P PMID: 5497814
  4. Voltage clamp analysis of acetylcholine produced end-plate current fluctuations at frog neuromuscular junction.
    J Physiol. 1973 Dec;235(3):655-91 PMID: 4543940
  5. Effects of membrane potential, temperature and neostigmine on the conductance change caused by a quantum or acetylcholine at the toad neuromuscular junction.
    J Physiol. 1975 Jan;244(2):385-407 PMID: 806678
  6. Fast kinetic studies on the interaction of cholinergic agonists with the membrane-bound acetylcholine receptor from Torpedo marmorata as revealed by quinacrine fluorescence.
    Eur J Biochem. 1977 Oct 17;80(1):225-42 PMID: 923575
  7. Differential effects of perhydrohistrionicotoxin on neurally and iontophoretically evoked endplate currents.
    Proc Natl Acad Sci U S A. 1978 Mar;75(3):1596-9 PMID: 206910
  8. On the mechanism of desensitization at cholinergic receptors.
    Mol Pharmacol. 1970 Jul;6(4):357-82 PMID: 5429280
  9. A new kind of drug antagonism: evidence that agonists cause a molecular change in acetylcholine receptors.
    Mol Pharmacol. 1969 Jul;5(4):394-411 PMID: 5805474
  10. Blocking effects of barium and hydrogen ions on the potassium current during anomalous rectification in the starfish egg.
    J Physiol. 1978 Jun;279:167-85 PMID: 566793
  11. A re-examination of curare action at the motor endplate.
    Proc R Soc Lond B Biol Sci. 1978 Dec 4;203(1151):119-33 PMID: 33387
  12. Drug blockade of open end-plate channels.
    J Physiol. 1976 Sep;260(3):531-52 PMID: 10432
  13. The characteristics of 'end-plate noise' produced by different depolarizing drugs.
    J Physiol. 1973 May;230(3):707-17 PMID: 4717155
  14. Interactions of aminopyridines with potassium channels of squid axon membranes.
    Biophys J. 1976 Jan;16(1):77-81 PMID: 1244890
  15. A study of the desensitization produced by acetylcholine at the motor end-plate.
    J Physiol. 1957 Aug 29;138(1):63-80 PMID: 13463799
  16. Studies on the electrogenic action of acetylcholine with Torpedo marmorata electric organ. V. Qualitative correlation between pharmacological effects and equilibration processes of the cholinergic receptor protein as revealed by the structural probe quinacrine.
    J Mol Biol. 1976 Sep 25;106(3):517-35 PMID: 978734
  17. Interaction of ligands with acetylcholinesterase. Use of temperature-jump relaxation kinetics in the binding of specific fluorescent ligands.
    Biochemistry. 1977 Aug 23;16(17):3870-8 PMID: 20130
  18. Analysis of atropine action at the frog neutromuscular junction.
    J Physiol. 1977 Jul;269(1):109-30 PMID: 302330
  19. The effect of voltage on the time course of end-plate currents.
    J Physiol. 1972 May;223(1):151-71 PMID: 4537943
  20. Interaction of a fluorescent probe with acetylcholine-activated synaptic membrane.
    Nature. 1977 Oct 13;269(5629):609-11 PMID: 917107
  21. Local anaesthetics transiently block currents through single acetylcholine-receptor channels.
    J Physiol. 1978 Apr;277:153-76 PMID: 306437
  22. Mode of action of quinacrine on the acetylcholine receptor ionic channel complex.
    Mol Pharmacol. 1979 Sep;16(2):382-92 PMID: 316101
  23. End-plate channel opening and the kinetics of quinacrine (mepacrine) block.
    J Physiol. 1980 Sep;306:283-306 PMID: 6257897
  24. Effect of histrionicotoxin on the ionic conductance modulator of the cholinergic receptor: a quantitative analysis of the end-plate current.
    J Pharmacol Exp Ther. 1974 May;189(2):513-24 PMID: 4545376
  25. Noise and relaxation studies of acetylcholine induced currents in the presence of procaine.
    J Physiol. 1978 May;278:237-50 PMID: 671293
  26. A study of desensitization using voltage clamp.
    Pflugers Arch. 1975 Oct 28;360(2):135-44 PMID: 1081218
  27. Kinetic analysis of end plate currents altered by atropine and scopolamine.
    Mol Pharmacol. 1978 May;14(3):514-29 PMID: 307112
  28. The relationship between desensitization and the metaphilic effect at cholinergic receptors.
    Mol Pharmacol. 1970 Jul;6(4):383-90 PMID: 5429281
  29. Effects of strychnine on the potassium conductance of the frog node of Ranvier.
    J Gen Physiol. 1977 Jun;69(6):897-914 PMID: 302320
  30. Interaction of tetraethylammonium ion derivatives with the potassium channels of giant axons.
    J Gen Physiol. 1971 Oct;58(4):413-37 PMID: 5112659
  31. Kinetic analysis of pancuronium interaction with sodium channels in squid axon membranes.
    J Gen Physiol. 1977 Mar;69(3):293-323 PMID: 845593
  32. The actions of tubocurarine at the frog neuromuscular junction.
    J Physiol. 1979 Aug;293:247-84 PMID: 315462
  33. The mode of action of antagonists of the excitatory response to acetylcholine in Aplysia neurones.
    J Physiol. 1978 May;278:207-35 PMID: 671288
  34. Ionic blockage of sodium channels in nerve.
    J Gen Physiol. 1973 Jun;61(6):687-708 PMID: 4541078
  35. Decamethonium both opens and blocks endplate channels.
    Proc Natl Acad Sci U S A. 1978 Jun;75(6):2994-8 PMID: 307251
  36. Interaction of proflavine and acriflavine with acetylcholinesterase.
    Eur J Biochem. 1973 Aug 17;37(2):377-88 PMID: 4745735
  37. Inactivation of the potassium conductance and related phenomena caused by quaternary ammonium ion injection in squid axons.
    J Gen Physiol. 1969 Nov;54(5):553-75 PMID: 5346528
  38. The effect of internal and external 4-aminopyridine on the potassium currents in intracellularly perfused squid giant axons.
    J Physiol. 1977 Jun;268(2):511-32 PMID: 874919
  39. Dynamics of 9-aminoacridine block of sodium channels in squid axons.
    J Gen Physiol. 1979 Jan;73(1):1-21 PMID: 438763
  40. The interaction of atebrin with phospholipid vesicles.
    Biochim Biophys Acta. 1975 Jan 14;375(1):22-34 PMID: 1111575
  41. Influence of SKF-525A congeners, strophanthidin and tissue-culture media on desensitization in frog skeletal muscle.
    Br J Pharmacol. 1974 Jun;51(2):259-68 PMID: 4155972
  42. Ion transport through pores: a rate-theory analysis.
    Biochim Biophys Acta. 1973 Jul 6;311(3):423-41 PMID: 4729828
  43. Local anesthetics. Effect of pH on use-dependent block of sodium channels in frog muscle.
    Biophys J. 1977 Dec;20(3):343-68 PMID: 21711
Article Info
Journal
The Journal of physiology
Abbr.
J Physiol
ISSN
0022-3751
Published
1980-09-00
Pages
261-81
Language
English
Region
England
NLM ID
0266262
PMCID
PMC1283005
Subset
IM
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