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By Baker, M. Blaustein, R. Keynes, Jacqueline Manil, T. Shaw, A. R., Steinhardt (1969)
The ouabain‐sensitive fluxes of sodium and potassium in squid giant axonsThe Journal of Physiology, 200
J. Nicholls, S. Kuffler (1964)
EXTRACELLULAR SPACE AS A PATHWAY FOR EXCHANGE BETWEEN BLOOD AND NEURONS IN THE CENTRAL NERVOUS SYSTEM OF THE LEECH: IONIC COMPOSITION OF GLIAL CELLS AND NEURONS.Journal of neurophysiology, 27
A. Stuart (1970)
Physiological and morphological properties of motoneurones in the central nervous system of the leechThe Journal of Physiology, 209
S. Nakajima, K. Takahashi (1966)
Post‐tetanic hyperpolarization and electrogenic Na pump in stretch receptor neurone of crayfishThe Journal of Physiology, 187
D. Baylor, J. Nicholls (1969)
Chemical and electrical synaptic connexions between cutaneous mechanoreceptor neurones in the central nervous system of the leechThe Journal of Physiology, 203
S. Kuffler, D. Potter (1964)
GLIA IN THE LEECH CENTRAL NERVOUS SYSTEM: PHYSIOLOGICAL PROPERTIES AND NEURON-GLIA RELATIONSHIP.Journal of neurophysiology, 27
R. Thomas (1969)
Membrane current and intracellular sodium changes in a snail neurone during extrusion of injected sodiumThe Journal of Physiology, 201
J. Nicholls, D. Baylor (1968)
Specific modalities and receptive fields of sensory neurons in CNS of the leech.Journal of neurophysiology, 31 5
Robert Meech (1972)
Intracellular calcium injection causes increased potassium conductance in Aplysia nerve cells.Comparative biochemistry and physiology. A, Comparative physiology, 42 2
D. Essen (1973)
The contribution of membrane hyperpolarization to adaptation and conduction block in sensory neurones of the leechThe Journal of Physiology, 230
H. Rang, J. Ritchie (1968)
On the electrogenic sodium pump in mammalian non‐myelinated nerve fibres and its activation by various external cationsThe Journal of Physiology, 196
B. Katz, R. Miledi (1967)
A study of synaptic transmission in the absence of nerve impulsesThe Journal of Physiology, 192
P. Caldwell (1968)
Factors governing movement and distribution of inorganic ions in nerve and muscle.Physiological reviews, 48 1
(1969)
The influence of calcium ions on sodium efflux in squid axons
R. Thomas (1968)
Measurement of current produced by the sodium pump in a snail neurone.The Journal of physiology, 195 2
M. Brodwick, D. Junge (1972)
Post‐stimulus hyperpolarization and slow potassium conductance increase in Aplysia giant neuroneThe Journal of Physiology, 223
G. Kerkut, R. Thomas (1965)
AN ELECTROGENIC SODIUM PUMP IN SNAIL NERVE CELLS.Comparative biochemistry and physiology, 14
J. Nicholls, D. Purves (1970)
Monosynaptic chemical and electrical connexions between sensory and motor cells in the central nervous system of the leechThe Journal of Physiology, 209
D. Baylor, J. Nicholls (1969)
Changes in extracellular potassium concentration produced by neuronal activity in the central nervous system of the leechThe Journal of Physiology, 203
P. Baker, A. Hodgkin, E. Ridgway (1971)
Depolarization and calcium entry in squid giant axonsThe Journal of Physiology, 218
D. Junge (1972)
Increased K-conductance as proximate cause of post-stimulus hyperpolarization in Tritonia neuronesComparative Biochemistry and Physiology Part A: Physiology, 42
(1967)
Surface density of calcium binding sites in the barnacle muscle fiber membrane
R. Thomas (1972)
Intracellular sodium activity and the sodium pump in snail neuronesThe Journal of Physiology, 220
D. Geduldig, D. Junge (1968)
Sodium and calcium components of action potentials in Aplysia giant neuroneThe Journal of Physiology, 199
D. Baylor, J. Nicholls (1969)
After‐effects of nerve impulses on signalling in the central nervous system of the leechThe Journal of Physiology, 203
J. Connor, C. Stevens (1971)
Prediction of repetitive firing behaviour from voltage clamp data on an isolated neurone somaThe Journal of Physiology, 213
Following trains of impulses, sensory neurones in the C.N.S. of the leech show a prolonged hyperpolarization, which lasts for seconds or minutes. In the present investigation the mechanisms that underly this hyperpolarization have been studied by recording intracellularly. Two factors have been found to be responsible. One is the activity of an electrogenic pump (see Baylor & Nicholls, 1969b); the other is a long‐lasting change in K conductance. 1. Additional evidence that an electrogenic pump contributes to a slow after‐hyperpolarization of leech sensory neurones is provided by the effects of injecting Na intracellularly. This leads to an increase in membrane potential that is blocked by the cardiac glycoside strophanthidin. Furthermore, after a train of impulses, reducing the K concentration in the external fluid characteristically reduces the hyperpolarizing action of the pump. 2. The hyperpolarization following impulses is associated with a reduction of the cell membrane resistance that can persist for several minutes. 3. Several lines of evidence suggest that the reduction in input resistance during the hyperpolarization is mainly due to an increased permeability to K. Thus, when the K concentration in Ringer fluid is reduced, the peak amplitude of the hyperpolarization following a train becomes larger. Furthermore, the conductance dependent part of the after‐hyperpolarization has a reversal potential close to the equilibrium potential for K (EK). Substitution of Cl by SO4 has little effect either on the after‐hyperpolarization or on the conductance change following a train. 4. Increased external Ca concentrations lead to a marked increase in the hyperpolarization that follows impulse activity. The enhanced hyperpolarization in high Ca is associated with a corresponding reduction in input resistance. The amplitude and duration of the hyperpolarization following a brief train of impulses can be increased by a factor of 5 or more in Ringer fluid containing 10 mM‐Ca instead of the usual 1·8 mM. The hyperpolarization and resistance changes still occur in solutions containing 20 mM‐Mg. 5. To augment the hyperpolarization the increased concentration of Ca must be present during the train of impulses. 6. The relative contributions of the K conductance increase and of the electrogenic pump for generating the hyperpolarization after impulse activity are different in the three types of sensory cell responding to touch, pressure and noxious stimulation.
The Journal of Physiology – Wiley
Published: Mar 1, 1973
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