The charge carried by single‐channel currents of rat cultured muscle cells in the presence of local anaesthetics.

Acetylcholine‐induced single‐channel currents were measured in the presence of the lignocaine derivative QX222. Unit responses appeared as bursts of short current pulses as a result of the fast blocking action of the drug (QX222). The amplitude of the individual current pulses was not changed by the presence of the drug up to a concentration of 250 microM. The time integral of current during a burst, which for a sequential blocking model should be independent of drug concentration, decreased at concentrations of QX222 higher than 40 microM. The distribution of gap times within a burst could not be fitted by a single exponential for high concentrations of QX222. It is concluded that the simple sequential model of channel blockade does not apply for concentrations of QX222 higher than 40 microM.

[1]  P. Ascher,et al.  The mode of action of antagonists of the excitatory response to acetylcholine in Aplysia neurones. , 1978, The Journal of physiology.

[2]  D. Colquhoun,et al.  The modes of action of gallamine , 1981, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[3]  B. Hille,et al.  Local anesthetics: hydrophilic and hydrophobic pathways for the drug- receptor reaction , 1977, The Journal of general physiology.

[4]  A G Hawkes,et al.  Relaxation and fluctuations of membrane currents that flow through drug-operated channels , 1977, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[5]  R. Ruff A quantitative analysis of local anaesthetic alteration of miniature end‐plate currents and end‐plate current fluctuations. , 1977, The Journal of physiology.

[6]  D. Gardner Time integral of synaptic conductance. , 1980, The Journal of physiology.

[7]  P. Adams Drug blockade of open end‐plate channels. , 1976, The Journal of physiology.

[8]  T. Narahashi,et al.  Endplate channel block by guanidine derivatives , 1981, The Journal of general physiology.

[9]  A. Hawkes,et al.  On the stochastic properties of bursts of single ion channel openings and of clusters of bursts. , 1982, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[10]  O. Hamill,et al.  Lifetime and conductance of acetylcholine‐activated channels in normal and denervated toad sartorius muscle. , 1980, The Journal of physiology.

[11]  K. Beam A quantitative description of end‐plate currents in the presence of two lidocaine derivatives. , 1976, The Journal of physiology.

[12]  K L Magleby,et al.  A quantitative description of end‐plate currents , 1972, The Journal of physiology.

[13]  E. Neher,et al.  Local anaesthetics transiently block currents through single acetylcholine‐receptor channels. , 1978, The Journal of physiology.

[14]  O. Hamill,et al.  Effects of anesthetics on ion channels in synapses. , 1981, International review of physiology.

[15]  B. Sakmann,et al.  Fluctuations in the microsecond time range of the current through single acetylcholine receptor ion channels , 1981, Nature.

[16]  B. Sakmann,et al.  Single-channel currents recorded from membrane of denervated frog muscle fibres , 1976, Nature.

[17]  R. Ruff The kinetics of local anesthetic blockade of end-plate channels. , 1982, Biophysical journal.

[18]  Fred J. Sigworth,et al.  An Example of Analysis , 1983 .

[19]  P. Adams,et al.  End‐plate channel opening and the kinetics of quinacrine (mepacrine) block. , 1980, The Journal of physiology.

[20]  P. Adams,et al.  Voltage jump analysis of procaine action at frog end‐plate , 1977, The Journal of physiology.