|
||
ARTICLE |
1. Intracellular injection of tetraethylammonium chloride (TEA) into a giant axon of the squid prolongs the duration of the action potential without changing the resting potential (Fig. 3). The prolongation is sometimes 100-fold or more.
2. The action potential of a giant axon treated with TEA has an initial peak followed by a plateau (Fig. 3). The membrane resistance during the plateau is practically normal (Fig. 4). Near the end of the action potential, there is an apparent increase in the membrane resistance (Fig. 5D and Fig. 6, right).
3. The phenomenon of abolition of action potentials was demonstrated in the squid giant axon treated with TEA (Fig. 7). Following an action potential abolished in its early phase, there is no refractoriness (Fig. 8).
4. By the method of voltage clamp, the voltage-current relation was investigated on normal squid axons as well as on axons treated with TEA (Figs. 9 and 10).
5. The presence of stable states of the membrane was demonstrated by clamping the membrane potential with two voltage steps (Fig. 11). Experimental evidence was presented showing that, in an "unstable" state, the membrane conductance is not uniquely determined by the membrane potential.
6. The effect of low sodium water was investigated in the axon treated with TEA (Fig. 12).
7. The similarity between the action potential of a squid axon under TEA and that of the vertebrate cardiac muscle was stressed. The experimental results were interpreted as supporting the view that there are two stable states in the membrane. Initiation and abolition of an action potential were explained as transitions between the two states.
Submitted on February 5, 1957
This article has been cited by other articles:
![]() |
H. C. Tuckwell Analytical and Simulation Results for the Stochastic Spatial Fitzhugh-Nagumo Model Neuron Neural Comput., December 1, 2008; 20(12): 3003 - 3033. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. H. Zhang, J. C. Fehrenbacher, M. R. Vasko, and G. D. Nicol Sphingosine-1-Phosphate Via Activation of a G-Protein-Coupled Receptor(s) Enhances the Excitability of Rat Sensory Neurons J Neurophysiol, September 1, 2006; 96(3): 1042 - 1052. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. L. Costantin and A. C. Charles Modulation of Ca2+ Signaling by K+ Channels in a Hypothalamic Neuronal Cell Line (GT1-1) J Neurophysiol, January 1, 2001; 85(1): 295 - 304. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Narahashi Neuroreceptors and Ion Channels as the Basis for Drug Action: Past, Present, and Future J. Pharmacol. Exp. Ther., July 1, 2000; 294(1): 1 - 26. [Abstract] [Full Text] |
||||
![]() |
A. Chrachri and R. Williamson Voltage-Dependent Conductances in Cephalopod Primary Sensory Hair Cells J Neurophysiol, December 1, 1997; 78(6): 3125 - 3132. [Abstract] [Full Text] [PDF] |
||||
![]() |
G Yellen, M. Jurman, T Abramson, and R MacKinnon Mutations affecting internal TEA blockade identify the probable pore-forming region of a K+ channel Science, February 22, 1991; 251(4996): 939 - 942. [Abstract] [PDF] |
||||
![]() |
T. Kondo Shortening of the Period of the Circadian Rhythm by a K+ Channel Blocker, Tetraethylammonium, in the Duckweed Lemna gibba G3 J Biol Rhythms, September 1, 1990; 5(3): 187 - 194. [Abstract] [PDF] |
||||
![]() |
K. Kusano, D. R. Livengood, and R. Werman Tetraethylammonium Ions: Effect of Presynaptic Injection on Synaptic Transmission Science, March 10, 1967; 155(3767): 1257 - 1259. [Abstract] [PDF] |
||||
![]() |
Y. Katsuki, K. Yanagisawa, and J. Kanzaki Tetraethylammonium and Tetrodotoxin: Effects on Cochlear Potentials Science, March 25, 1966; 151(3717): 1544 - 1545. [Abstract] [PDF] |
||||
![]() |
C. S. SPYROPOULOS and R. O. BRADY Prolongation of Response of Node of Ranvier by Metal Ions Science, May 15, 1959; 129(3359): 1366 - 1367. [Abstract] [PDF] |
||||
![]() |
I. TASAKI and A. BAK Oscillatory Membrane Currents of Squid Giant Axon under Voltage-Clamp Science, October 11, 1957; 126(3276): 696 - 697. [PDF] |
||||
|
|