Literature DB >> 4838796

Changes of extracellular potassium concentration induced by neuronal activity in the sinal cord of the cat.

N Kríz, E Syková, E Ujec, L Vyklický.   

Abstract

1. Changes of extracellular K(+) concentration, [K](e), arising in the spinal cord of the cat in response to an afferent stimulation were studied by means of K(+)-specific micro-electrodes.2. In the most active areas of the spinal cord a single volley in a large afferent input like the common peroneal nerve or the posterior tibial nerve produced a transient increase in [K](e) of 0.05-0.1 mM, which reached its peak in 0.2-0.3 sec and it declined in about 3 sec.3. Much higher increases in [K](e) were found during repetitive stimulation of an afferent input. The highest increase (by 3 mM) was at 100 Hz, but even at 1 Hz a significant increase of 0.25 mM was observed. Equilibration of accumulated K(+) was slow with a time constant of about 6 sec, which is much longer than could be expected for the same process in free solution.4. A characteristic distribution of increased [K](e) was found in the spinal cord in response to 100 Hz afferent stimulation. The highest increase of 3 mM was found in and around the intermediate nucleus, but at depths between 0.9-1.8 mm the [K](e) increase exceeded 1 mM.5. In the ventral horns afferent stimulation (100 Hz) increased [K](e) by 0.25 mM, while the same stimulation of the ventral root resulted in a [K](e) increase of less than 0.05 mM.6. The consequences of K(e) (+) accumulation after neuronal discharge are discussed in respect to its possible role in the depolarization of primary afferent terminals.

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Year:  1974        PMID: 4838796      PMCID: PMC1330859          DOI: 10.1113/jphysiol.1974.sp010507

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  23 in total

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Authors:  J C ECCLES; R M ECCLES; F MAGNI
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2.  A morphological basis for pre-synaptic inhibition?

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3.  Reduction of transmitter output by depolarization.

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4.  Excitability changes in afferent fibre terminations and their relation to slow potentials.

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Journal:  J Physiol       Date:  1958-06-18       Impact factor: 5.182

5.  The interpretation of potential changes in the spinal cord.

Authors:  D H Barron; B H Matthews
Journal:  J Physiol       Date:  1938-04-14       Impact factor: 5.182

6.  The sodium and potassium content of cephalopod nerve fibers.

Authors:  R D KEYNES; P R LEWIS
Journal:  J Physiol       Date:  1951-06       Impact factor: 5.182

7.  Differential high-impedance DC amplifier with negative input capacity.

Authors:  E Ujec; R Beránek
Journal:  Physiol Bohemoslov       Date:  1967

8.  Work-induced increase of extracellular potassium concentration in muscle measured by ion-specific electrodes.

Authors:  P Hnik; F Vyskocil; N Kriz; M Holas
Journal:  Brain Res       Date:  1972-05-26       Impact factor: 3.252

9.  Changes in extracellular potassium concentration produced by neuronal activity in the central nervous system of the leech.

Authors:  D A Baylor; J G Nicholls
Journal:  J Physiol       Date:  1969-08       Impact factor: 5.182

10.  Effect of nerve impulses on the membrane potential of glial cells in the central nervous system of amphibia.

Authors:  R K Orkand; J G Nicholls; S W Kuffler
Journal:  J Neurophysiol       Date:  1966-07       Impact factor: 2.714

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  37 in total

1.  Extracellular potassium activity, intracellular and extracellular potential responses in the spinal cord.

Authors:  E W Lothman; G G Somjen
Journal:  J Physiol       Date:  1975-10       Impact factor: 5.182

2.  Extracellular potassium and trasmitter release at the giant synapse of squid.

Authors:  S D Erulkar; F F Weight
Journal:  J Physiol       Date:  1977-04       Impact factor: 5.182

3.  Spread of the dorsal root potentials in lower lumbar, sacral and upper caudal spinal cord.

Authors:  K Lupa; G Wójcik; M Ozóg; A Niechaj
Journal:  Pflugers Arch       Date:  1979-09       Impact factor: 3.657

4.  Dorsal root potentials and changes in extracellular potassium in the spinal cord of the frog.

Authors:  R A Nicoll
Journal:  J Physiol       Date:  1979-05       Impact factor: 5.182

5.  Extracellular potassium changes in the spinal cord of the cat and their relation to slow potentials, active transport and impulse transmission.

Authors:  N Krív; E Syková; L Vyklický
Journal:  J Physiol       Date:  1975-07       Impact factor: 5.182

6.  Studies on convulsants in the isolated frog spinal cord. II. Effects on root potentials.

Authors:  J L Barker; R A Nicoll; A Padjen
Journal:  J Physiol       Date:  1975-03       Impact factor: 5.182

Review 7.  Diffusion in brain extracellular space.

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8.  High frequency stimulation extends the refractory period and generates axonal block in the rat hippocampus.

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9.  Precocious development of glucuronidating and hydroxylating enzymes in chick embryos treated with pituitary grafts.

Authors:  G J Wishart; G J Dutton
Journal:  Biochem J       Date:  1975-11       Impact factor: 3.857

10.  Activity-dependent changes in extracellular Ca2+ and K+ reveal pacemakers in the spinal locomotor-related network.

Authors:  Frédéric Brocard; Natalia A Shevtsova; Mouloud Bouhadfane; Sabrina Tazerart; Uwe Heinemann; Ilya A Rybak; Laurent Vinay
Journal:  Neuron       Date:  2013-03-20       Impact factor: 17.173

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