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1. Rohon-Beard cells in the spinal cord of Xenopus laevis tadpoles have been studied in animals 4-days to 2-weeks-old (Nieuwkoop & Faber, 1956, stages 45-49). These neurones have an unusually large resting membrane potential of -88 mV, in Ringer solution containing 3-0 mM K+. 2. Their resting potential (R..) depends on the concentration gradient of K+ across the cell membrane. These cells follow the prediction of the Nernst equation for a K+-selective electrode, down to external K+ concentrations as low as 1-0 mM (R.P. -118 mV). 3. The resting potentials of muscle cells in these animals exhibit the same dependence on external [K+], as has been shown previously. 4. Rohon-Beard cells can be driven antidromically, bu stimulation of the anterior end of the spinal cord with brief current pulses through a suction electrode. Antidromic action potentials fail to invade the cell body with repeated stimulation at 1Hz. 5. Even when impulses fail to invade Rohon-Beard somata, slow depolarizations can be produced by single shocks or trains of shocks which cause impulse activity in other neurones. The response can be observed to a single stimulus or to a train of stimuli. The magnitude of the depolarization is graded, depending on the number of stimuli and the frequency of stimulation. 6. Support is presented for the hypothesis that the slow depolarization in Rohon-Beard cells is mediated by the release of K+ into their environment by the impulse activity of neighbouring neurones. The slow depolarization increases in solutions containing 1-5 mM-K+, and decreases in solutions containing 6-0 mM-K+. The changes are in quantitative agreement with those anticipated by theory. 7. The slow depolarization is unlikely to be due to a conductance change produced by a synaptic transmitter, since hyperpolarization and depolarization of the Rohon-Beard cell with injected current do not change the amplitude of the response. Further, low Ca-high Mg solutions which block neuromuscular transmission do not block the response. 8. The possible role of the slow depolarizing response in the physiological activity of these neurones is discussed.
Barron,
The interpretation of potential changes in the spinal cord.
1938, Pubmed
Barron,
The interpretation of potential changes in the spinal cord.
1938,
Pubmed
Baylor,
Changes in extracellular potassium concentration produced by neuronal activity in the central nervous system of the leech.
1969,
Pubmed
Baylor,
After-effects of nerve impulses on signalling in the central nervous system of the leech.
1969,
Pubmed
Cohen,
Ionic environment of neurones and glial cells in the brain of an amphibian.
1968,
Pubmed
CONWAY,
Nature and significance of concentration relations of potassium and sodium ions in skeletal muscle.
1957,
Pubmed
de Laat,
New membrane formation during cytokinesis in normal and cytochalasin B-treated eggs of Xenopus laevis. II. Electrophysiological observations.
1974,
Pubmed
,
Xenbase
Dennis,
Synaptic transmission and its duplication by focally applied acetylcholine in parasympathetic neurons in the heart of the frog.
1971,
Pubmed
Fischbach,
Electrophysiologic and morphologic properties of neurons in dissociated chick spinal cord cell cultures.
1974,
Pubmed
FRANKENHAEUSER,
The after-effects of impulses in the giant nerve fibres of Loligo.
1956,
Pubmed
Gorman,
Steady-state contribution of the sodium pump to the resting potential of a molluscan neurone.
1974,
Pubmed
HUGHES,
The development of the primary sensory system in Xenopus laevis (Daudin).
1957,
Pubmed
,
Xenbase
HUXLEY,
Effect of potassium and sodium on resting and action potentials of single myelinated nerve fibers.
1951,
Pubmed
Keynes,
The movements of labelled ions in mammalian non-myelinated nerve fibres.
1965,
Pubmed
Kríz,
Changes of extracellular potassium concentration induced by neuronal activity in the sinal cord of the cat.
1974,
Pubmed
Krnjević,
Extracellular K + activity and slow potential changes in spinal cord and medulla.
1972,
Pubmed
Kuffler,
Physiological properties of glial cells in the central nervous system of amphibia.
1966,
Pubmed
Martin,
Sensory cells in the spinal cord of the sea lamprey.
1971,
Pubmed
McMahan,
Visual identification of synaptic boutons on living ganglion cells and of varicosities in postganglionic axons in the heart of the frog.
1971,
Pubmed
O'Lague,
Evidence for cholinergic synapses between dissociated rat sympathetic neurons in cell culture.
1974,
Pubmed
Orkand,
Effect of nerve impulses on the membrane potential of glial cells in the central nervous system of amphibia.
1966,
Pubmed
Palmer,
Some bio-electric parameters of early Xenopus embryos.
1970,
Pubmed
,
Xenbase
Rovainen,
Physiological and anatomical studies on large neurons of central nervous system of the sea lamprey (Petromyzon marinus). II. Dorsal cells and giant interneurons.
1967,
Pubmed
Slack,
The distribution of sodium and potassium in amphibian embryos during early development.
1973,
Pubmed
,
Xenbase
Slack,
Intracellular and intercellular potentials in the early amphibian embryo.
1973,
Pubmed
,
Xenbase
Somjen,
Potassium, sustained focal potential shifts, and dorsal root potentials of the mammalian spinal cord.
1974,
Pubmed
Varon,
Excitability and conduction in neurons of dissociated ganglionic cell cultures.
1971,
Pubmed
Vyklicky,
Post-stimulation changes of extracellular potassium concentration in the spinal cord of the rat.
1972,
Pubmed