Abstract
1. The actions of amylobarbitone, thiopentone, methohexitone and methyprylone at voltage-clamped frog end-plates were studied. 2. In the presence of barbiturates the conductance change evoked by an iontophoretic carbachol application was reduced by a prepulse of carbachol. The extra inhibition evoked by a prepulse disappeared exponentially with a time constant of 150-200 ms. 3. Barbiturates produce an increased rate of decay of nerve evoked endplate currents. Tne concentration and voltage dependence of the barbtiruate e.p.c. decay rates tally with the hypothesis that the increased rate of decay is due to block of active receptor-channel complexes by barbiturates with a rate constant of 10(6) M-1S-1. 4. Conductance changes produced by bath applied agonists were depressed by thiopentone, the effect becoming greater the higher the agonist concentration. This effect, and also the observation that the concentration of thiopentone required to depress the bath agonist response is much greater than the apparent dissociation constant for binding to active receptor-channel complexes calculated from kinetic measurements, suggest that the selectivity for binding to open receptor-channel complexes is very high. 5. Methyprylone, which is structurally similar to the barbiturates, is only a weak antagonist and shows no interpulse interaction. It was predicted that methyprylone should produce fast and slow components in the e.p.c. decay, and this prediction was verified. 6. In the presence of barbiturates large iontophoretic carbachol applications produce conductance changes which show fast and slow components. Under these conditions the effects of carbachol prepulses become complex. However the effects are qualitatively consistent with the notion that different components of the response are contributed by channels located at various distances from the iontophoretic pipette tip. 7. All the data agree with a model in which the channel has three stages: closed, open and blocked. Only open channels can block, and blocked channels can only open.
MeSH Terms
Acetylcholine/antagonists & inhibitors
Amobarbital/pharmacology
Animals
Barbiturates/pharmacology
Carbachol/pharmacology
Dose-Response Relationship, Drug
Electric Conductivity
Hydrogen-Ion Concentration
In Vitro Techniques
Iontophoresis
Membrane Potentials/drug effects
Methohexital/pharmacology
Motor Endplate/drug effects
Neuromuscular Junction/drug effects
Piperidones/pharmacology
Rana pipiens
Rana temporaria
Thiopental/pharmacology
Tubocurarine/pharmacology
Chemicals
Barbiturates
Piperidones
Carbachol
Methohexital
Amobarbital
Thiopental
Acetylcholine
Tubocurarine
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Adams P R
References (28)
28 references, click to expand
-
Mechanism of blockade of neuromuscular transmission by pentobarbital.
J Pharmacol Exp Ther. 1975 Jan;192(1):95-104
PMID: 164531
-
Voltage dependence of agonist responses at voltage-clamped frog endplates.
Pflugers Arch. 1976 Jan 30;361(2):145-51
PMID: 943088
-
Voltage dependence of agonist effectiveness at the frog neuromuscular junction: resolution of a paradox.
J Physiol. 1975 Oct;251(2):245-70
PMID: 1081139
-
A model for the procaine end-plate current.
J Physiol. 1975 Mar;246(2):61P-63P
PMID: 1142273
-
CNS depressants: effects on post-synaptic pharmacology.
Brain Res. 1975 Jul 4;92(1):35-55
PMID: 1174946
-
An analysis of the dose-response curve at voltage-clamped frog-endplates.
Pflugers Arch. 1975 Oct 28;360(2):145-53
PMID: 1237869
-
Drug interactions at the motor endplate.
Pflugers Arch. 1975 Oct 28;360(2):155-64
PMID: 1237870
-
The effect of anesthetic agents on skeletal muscle membrane.
Acta Physiol Scand. 1956 Nov 5;37(4):335-49
PMID: 13372366
-
A kinetic model for the action of xylocaine on receptors for acetylcholine.
J Gen Physiol. 1968 Jul;52(1):162-80
PMID: 4316946
-
Difference in effects of end-plate potentials between procaine and lidocaine as revealed by voltage-clamp experiments.
J Neurophysiol. 1971 Jan;34(1):32-46
PMID: 4322252
-
Barbiturate-induced transmitter release at a frog neuromuscular junction.
Br J Pharmacol. 1973 May;48(1):48-58
PMID: 4353318
-
The effect of voltage on the time course of end-plate currents.
J Physiol. 1972 May;223(1):151-71
PMID: 4537943
-
Ionic blockage of sodium channels in nerve.
J Gen Physiol. 1973 Jun;61(6):687-708
PMID: 4541078
-
The inhibition of sodium currents in myelinated nerve by quaternary derivatives of lidocaine.
J Gen Physiol. 1973 Jul;62(1):37-57
PMID: 4541340
-
Influence of chloride ions on changes in membrane potential during prolonged application of carbachol to frog skeletal muscle.
Br J Pharmacol. 1973 Feb;47(2):363-76
PMID: 4541779
-
The rate of action of tetrodotoxin on myelinated nerve fibres of Xenopus laevis and Rana esculenta.
J Physiol. 1973 Aug;233(1):167-94
PMID: 4543328
-
Voltage clamp analysis of acetylcholine produced end-plate current fluctuations at frog neuromuscular junction.
J Physiol. 1973 Dec;235(3):655-91
PMID: 4543940
-
Allosteric mechanisms at neuromuscular junctions.
Neurosci Res Program Bull. 1973 Jun;11(3):220-4
PMID: 4736777
-
A quantitative description of end-plate currents.
J Physiol. 1972 May;223(1):173-97
PMID: 5046143
-
Interaction of tetraethylammonium ion derivatives with the potassium channels of giant axons.
J Gen Physiol. 1971 Oct;58(4):413-37
PMID: 5112659
-
[Effect of some membrane stabilizers on the function of the neuromuscular synapse].
Fiziol Zh SSSR Im I M Sechenova. 1971 Sep;57(9):1313-21
PMID: 5316014
-
Extrinsic and intrinsic acetylcholine and barbiturate effects on frog skeletal muscle.
Br J Pharmacol. 1970 Nov;40(3):552P-553P
PMID: 5497814
-
Effects of procaine on ionic conductances of end-plate membranes.
J Pharmacol Exp Ther. 1971 Feb;176(2):423-33
PMID: 5568785
-
Barbiturates block sodium and potassium conductance increases in voltage-clamped lobster axons.
J Gen Physiol. 1968 Mar;51(3):293-307
PMID: 5648829
-
The effect of membrane polarization on the time course of the end-plate current in frog sartorius muscle.
J Physiol. 1969 Oct;204(2):493-502
PMID: 5824649
-
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
-
Effects of some aliphatic alcohols on the conductance change caused by a quantum of acetylcholine at the toad end-plate.
J Physiol. 1975 Jan;244(2):409-29
PMID: 806679
-
Alteration by xylocaine (lidocaine) and its derivatives of the time course of the end plate potential.
J Gen Physiol. 1968 Jul;52(1):144-61
PMID: 4316945