Literature DB >> 1202194

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

E W Lothman, G G Somjen.   

Abstract

1. Microcapillary electrode assemblies of two or three channels were used to record extracellular and intracellular potentials together with the extracellular activity of potassium ions, from essentially single locations within the substance of the decapitate spinal cord of cats. A liquid ion exchanger filled the tip of the potassium sensing microprobe. Activity was evoked by electrical stimulation of afferent peripheral nerves (ventral roots were cut). 2. Within the substance of the spinal grey matter increments of extracellular potassium activity evoked by repetitive afferent volleys were precisely correlated with magnitudes of sustained shifts of extracellular electric potential. Raising [K+]o from 3 to 4 mM was associated with a negative shift of potential of 2-5 +/- 0-5 mV, regardless of the position of the electrode in the tissue, and regardless of treatment by convulsant or depressant drugs. 3. The spatial distribution of the responses of potassium activity was mapped by the spatial distribution of the negative sustained potential shifts. 4. Depolarization shifts of potential recorded from within neuroglia cells ran parallel with changes of extracellular potassium potential. Even though the magnitude of extracellular sustained potential shifts was precisely correlated with the responses of both extracellular potassium and intracellular glial potentials, the trajectory of sustained potential shifts did not exactly mirror the two other variables. Onset and offset of sustained potential shifts were faster than those of glial potentials or of extracellular potassium. 5. The responses of the true transmembrane potential (intracellular less extracellular potential shifts) of neuroglia cells in the spinal grey matter can fully be described by the Nernst equation. 6. Membrane potentials of neurones, potentials recorded from dorsal root filaments, or from white matter, appeared unrelated to the activity of potassium ions in extracellular fluid. 7. The results are compatible with the suggestions that changes of the membrane potential of spinal neuroglia cells are fully determined by the change of the activity of extracellular potassium, and that glia cells supply most of the current which generates sustained shifts of the extracellular potential of spinal grey matter. The results are hard to reconcile with suggestions that under conditions of moderate excitation (i.e. in the absence of convulsive neuronal activity) changes of extracellular potassium would significantly influence the membrane potential of spinal neurones, or of primary afferent nerve fibres.

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Year:  1975        PMID: 1202194      PMCID: PMC1348471          DOI: 10.1113/jphysiol.1975.sp011137

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


  37 in total

1.  Slow potentials induced by changes of extracellular potassium in the spinal cord of the cat.

Authors:  L Vyklický; E Syková; N Kríz
Journal:  Brain Res       Date:  1975-04-04       Impact factor: 3.252

2.  NADH fluorescence and [K+]o changes during hippocampal electrical stimulation.

Authors:  D V Lewis; W H Schuette
Journal:  J Neurophysiol       Date:  1975-03       Impact factor: 2.714

3.  Post-stimulation changes of extracellular potassium concentration in the spinal cord of the rat.

Authors:  L Vyklicky; E Sykova; N Kriz; E Ujec
Journal:  Brain Res       Date:  1972-10-27       Impact factor: 3.252

4.  Evoked sustained focal potentials and membrane potential of neurons and of unresponsive cells of the spinal cord.

Authors:  G G Somjen
Journal:  J Neurophysiol       Date:  1970-07       Impact factor: 2.714

5.  Intracellular potentials from "idle" cells in cerebral cortex of cat.

Authors:  Y Karahashi; S Goldring
Journal:  Electroencephalogr Clin Neurophysiol       Date:  1966-06

6.  Extracellular accumulation of K+ evoked by activity of primary afferent fibers in the cuneate nucleus and dorsal horn of cats.

Authors:  K Krnjević; M E Morris
Journal:  Can J Physiol Pharmacol       Date:  1974-08       Impact factor: 2.273

7.  Possible relationships between extracellular potassium activity and presynaptic inhibition in the spinal cord of the cat.

Authors:  G ten Bruggencate; H D Lux; L Liebl
Journal:  Pflugers Arch       Date:  1974       Impact factor: 3.657

8.  Depression of sustained evoked potentials and glial depolarization in the spinal cord by barbiturates and by diphenylhydantoin.

Authors:  W J Strittmatter; G G Somjen
Journal:  Brain Res       Date:  1973-06-15       Impact factor: 3.252

9.  The equilibration time course of (K + ) 0 in cat cortex.

Authors:  H D Lux; E Neher
Journal:  Exp Brain Res       Date:  1973-04-30       Impact factor: 1.972

10.  Extracellular K + activity and slow potential changes in spinal cord and medulla.

Authors:  K Krnjević; M E Morris
Journal:  Can J Physiol Pharmacol       Date:  1972-12       Impact factor: 2.273

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  34 in total

1.  Spatial buffering of potassium ions in brain extracellular space.

Authors:  K C Chen; C Nicholson
Journal:  Biophys J       Date:  2000-06       Impact factor: 4.033

2.  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

3.  Long-lasting GABA-mediated depolarization evoked by high-frequency stimulation in pyramidal neurons of rat hippocampal slice is attributable to a network-driven, bicarbonate-dependent K+ transient.

Authors:  K Kaila; K Lamsa; S Smirnov; T Taira; J Voipio
Journal:  J Neurosci       Date:  1997-10-15       Impact factor: 6.167

4.  Cortico-spinal connections in the rat. II. Oligosynaptic and polysynaptic responses of lumbar motoneurons to epicortical stimulation.

Authors:  R W Janzen; E J Speckmann; H Caspers; C E Elger
Journal:  Exp Brain Res       Date:  1977-06-27       Impact factor: 1.972

5.  The release of endogenous amino acids from the rat visual cortex.

Authors:  R M Clark; G G Collins
Journal:  J Physiol       Date:  1976-11       Impact factor: 5.182

6.  Activity-dependent modulation of K+ currents at presynaptic terminals of mammalian central synapses.

Authors:  J Qian; P Saggau
Journal:  J Physiol       Date:  1999-09-01       Impact factor: 5.182

7.  Slow waves and unitary activity evoked by cutaneous stimulation from the rat cuneate nucleus.

Authors:  M Armstrong-James; W R Ewart
Journal:  Exp Brain Res       Date:  1980       Impact factor: 1.972

8.  Slow depolarizing potentials recorded from glial cells in the rat superficial dorsal horn.

Authors:  T Takahashi; H Tsuruhara
Journal:  J Physiol       Date:  1987-07       Impact factor: 5.182

9.  Primary afferent activity, putative excitatory transmitters and extracellular potassium levels in frog spinal cord.

Authors:  R A Davidoff; J C Hackman; A M Holohean; J L Vega; D X Zhang
Journal:  J Physiol       Date:  1988-03       Impact factor: 5.182

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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