Literature DB >> 5499812

The contribution by glial cells to surface recordings from the optic nerve of an amphibian.

M W Cohen.   

Abstract

1. The contribution by glial cells to surface recordings has been examined in the optic nerve of the amphibian Necturus maculosus. The method of current injection was employed selectively to alter the membrane potential of glial cells without affecting that of the axons. The resulting changes in potential were recorded simultaneously from the surface of the nerve using the sucrose gap method and intracellularly from a glial cell near the gap.2. The sucrose gap method recorded 40% of the changes in glial membrane potential. This percentage was not affected when the current electrode was inserted into different glial cells while maintaining the recording conditions constant.3. Following axonal degeneration, produced by removing the eye 2-3 months earlier, the percentage contribution by glia increased to 84%.4. By measuring sucrose gap responses to changes in K(o) it was possible to estimate that the sucrose gap method recorded 31-60% of changes in axonal membrane potential. It was also determined that the axons, unlike glial cells, are relatively insensitive to reductions in K(o). Surface responses to decreases in external potassium thus reflect the magnitude of the glial contribution.5. It is concluded that changes in glial membrane potential contribute about as much to surface recordings from the optic nerve of Necturus as do equivalent changes in axonal membrane potential. The contributions by the glial cells and axons are related to the relative volumes of tissue they respectively occupy. The significance of these findings to the analysis of surface recordings from the mammalian brain is discussed. Since mammalian glial cells, like those in Amphibia and the leech, become depolarized during neuronal activity and on the basis of electron microscopic evidence appear to be electrically coupled, it is likely that they contribute to the electroencephalogram.

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Year:  1970        PMID: 5499812      PMCID: PMC1395601          DOI: 10.1113/jphysiol.1970.sp009227

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


  22 in total

1.  GLIA IN THE LEECH CENTRAL NERVOUS SYSTEM: PHYSIOLOGICAL PROPERTIES AND NEURON-GLIA RELATIONSHIP.

Authors:  S W KUFFLER; D D POTTER
Journal:  J Neurophysiol       Date:  1964-03       Impact factor: 2.714

2.  A new method for measuring membrane potentials with external electrodes.

Authors:  R STAMPFLI
Journal:  Experientia       Date:  1954-12-15

3.  The influence of potassium and chloride ions on the membrane potential of single muscle fibres.

Authors:  A L HODGKIN; P HOROWICZ
Journal:  J Physiol       Date:  1959-10       Impact factor: 5.182

4.  Plasma membrane contacts in the central nervous system.

Authors:  A PETERS
Journal:  J Anat       Date:  1962-04       Impact factor: 2.610

5.  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

6.  Depolarization of cortical glial cells during electrocortical activity.

Authors:  R G Grossman; T Hampton
Journal:  Brain Res       Date:  1968-11       Impact factor: 3.252

7.  Unresponsive cells in cerebral cortex.

Authors:  J S Kelly; K Krnjević; G K Yim
Journal:  Brain Res       Date:  1967-12       Impact factor: 3.252

8.  Physiological properties of glial cells in the central nervous system of amphibia.

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

9.  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

10.  Some physiological properties of identified mammalian neuroglial cells.

Authors:  M J Dennis; H M Gerschenfeld
Journal:  J Physiol       Date:  1969-07       Impact factor: 5.182

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  8 in total

1.  Oscillatory potentials as predictors to amplitude and peak time of the photopic b-wave of the human electroretinogram.

Authors:  P Lachapelle
Journal:  Doc Ophthalmol       Date:  1990-08       Impact factor: 2.379

2.  Components of the electroretinogram: a reappraisal.

Authors:  P Lachapelle; S Molotchnikoff
Journal:  Doc Ophthalmol       Date:  1986-11-15       Impact factor: 2.379

3.  Noninactivating, tetrodotoxin-sensitive Na+ conductance in rat optic nerve axons.

Authors:  P K Stys; H Sontheimer; B R Ransom; S G Waxman
Journal:  Proc Natl Acad Sci U S A       Date:  1993-08-01       Impact factor: 11.205

4.  Regional specialization of retinal glial cell membrane.

Authors:  E A Newman
Journal:  Nature       Date:  1984 May 10-16       Impact factor: 49.962

5.  Primary afferent depolarization in the in vitro frog olfactory bulb.

Authors:  C E Jahr; R A Nicoll
Journal:  J Physiol       Date:  1981-09       Impact factor: 5.182

6.  Presynaptic gamma-aminobutyric acid responses in the olfactory cortex.

Authors:  H G Pickles
Journal:  Br J Pharmacol       Date:  1979-02       Impact factor: 8.739

7.  Effects of barium and bicarbonate on glial cells of Necturus optic nerve. Studies with microelectrodes and voltage-sensitive dyes.

Authors:  M L Astion; A L Obaid; R K Orkand
Journal:  J Gen Physiol       Date:  1989-04       Impact factor: 4.086

8.  Slow PIII component of the carp electroretinogram.

Authors:  P Witkovsky; F E Dudek; H Ripps
Journal:  J Gen Physiol       Date:  1975-02       Impact factor: 4.086

  8 in total

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