Literature DB >> 3876405

Light-evoked increases in extracellular K+ in the plexiform layers of amphibian retinas.

C J Karwoski, E A Newman, H Shimazaki, L M Proenza.   

Abstract

Recordings of light-evoked changes in extracellular K+ concentration (delta[K+]o) were obtained in the retinas of frog and mudpuppy. In eyecup preparations, various recording approaches were used and provided evidence for a K increase near the outer plexiform layer (distal K increase). This distal K increase could be pharmacologically dissociated from the well-known, large K increase in the proximal retina by the application of ethanol and gamma-aminobutyric acid. The distal K increase also often showed surround antagonism. A retinal slice preparation was used to permit electrode placement into the desired retinal layers under direct visual control and without the risk of electrode damage to adjacent layers. In the slice, a distinct distal K increase was found in the outer plexiform layer, in addition to the prominent K increase in the inner plexiform layer. Compared with eyecups, only weak K increases were found in the nuclear layers of the slice. This suggests that the K responses observed in the nuclear layers of eyecups may be generated by K+ diffusing along the electrode track from the plexiform layers. In the context of current models of ERG b-wave generation, the magnitude of the recorded distal K increase, compared with the proximal K increase, seems too small to give rise to the b-wave. However, the distal K increase may be differentially depressed by electrode dead space. It is also possible that if certain aspects of the models of b-wave generation were modified, then the observed distal K increase could give rise to the b-wave.

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Year:  1985        PMID: 3876405      PMCID: PMC2228783          DOI: 10.1085/jgp.86.2.189

Source DB:  PubMed          Journal:  J Gen Physiol        ISSN: 0022-1295            Impact factor:   4.086


  18 in total

1.  K(+)-evoked Müller cell depolarization generates b-wave of electroretinogram in toad retina.

Authors:  R Wen; B Oakley
Journal:  Proc Natl Acad Sci U S A       Date:  1990-03       Impact factor: 11.205

Review 2.  Potassium buffering in the central nervous system.

Authors:  P Kofuji; E A Newman
Journal:  Neuroscience       Date:  2004       Impact factor: 3.590

Review 3.  Cellular and physiological mechanisms underlying blood flow regulation in the retina and choroid in health and disease.

Authors:  Joanna Kur; Eric A Newman; Tailoi Chan-Ling
Journal:  Prog Retin Eye Res       Date:  2012-05-03       Impact factor: 21.198

Review 4.  Astrocyte regulation of blood flow in the brain.

Authors:  Brian A MacVicar; Eric A Newman
Journal:  Cold Spring Harb Perspect Biol       Date:  2015-03-27       Impact factor: 10.005

5.  Evidence for the uptake of neuronally derived choline by glial cells in the leech central nervous system.

Authors:  W A Wuttke; V W Pentreath
Journal:  J Physiol       Date:  1990-01       Impact factor: 5.182

6.  Efficient K+ buffering by mammalian retinal glial cells is due to cooperation of specialized ion channels.

Authors:  B Nilius; A Reichenbach
Journal:  Pflugers Arch       Date:  1988-06       Impact factor: 3.657

7.  Bias current modifies the selectivity of liquid membrane ion-selective microelectrodes.

Authors:  J A Coles
Journal:  Pflugers Arch       Date:  1988-03       Impact factor: 3.657

8.  Spatial Organization and Dynamics of the Extracellular Space in the Mouse Retina.

Authors:  Sidney P Kuo; Pei-Pei Chiang; Amy R Nippert; Eric A Newman
Journal:  J Neurosci       Date:  2020-09-04       Impact factor: 6.167

9.  Extracellular pH in the isolated retina of the toad in darkness and during illumination.

Authors:  B Oakley; R Wen
Journal:  J Physiol       Date:  1989-12       Impact factor: 5.182

10.  Metabotropic glutamate receptor-mediated suppression of an inward rectifier current is linked via a cGMP cascade.

Authors:  D B Dixon; D R Copenhagen
Journal:  J Neurosci       Date:  1997-12-01       Impact factor: 6.167

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