Literature DB >> 119827

Effects of the rod receptor potential upon retinal extracellular potassium concentration.

B Oakley, D G Flaming, K T Brown.   

Abstract

It has been hypothesized that the light-evoked rod hyperpolarization (the receptor potential) initiates the light-evoked decrease in extracellular potassium ion concentration, [K+]o, in the distal retina. The hypothesis was tested using the isolated, superfused retina of the toad, Bufo marinus; the receptor potential was recorded intracellularly from red rods, and [K+]o was measured in the photoreceptor layer with K+-specific microelectrodes. In support of the hypothesis, variations in stimulus irradiance or duration, or in retinal temperature, produced qualitatively similar effects on both the receptor potential and the decrease in [K+]o. A mechanism for the relationship between the receptor potential and the decrease in [K+]o was suggested by Matsuura et al. (1978. Vision Res. 18:767-775). In the dark, the passive efflux of K+ out of the rod is balanced by an equal influx of K+ fromthe Na+/K+ pump. The light-evoked rod hyperpolarization is assumed to reduce the passive efflux, with little effect on the pump. Thus, the influx will exceed the efflux, and [K+]o will decrease. Consistent with this mechanism, the largest and most rapid decrease in [K+]o was measured adjacent to the rod inner segments, where the Na+/K+ pump is most likely located; in addition, inhibition of the pump with ouabain abolished the decrease in [K]o more rapidly than the rod hyperpolarization. Based upon this mechanism, Matsuura et al. (1978) developed a mathematical model: over a wide range of stimulus irradiance, this model successfully predicts the time-course of the decrease in [K+]o, given only the time-course of the rod hyperpolarization.

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Year:  1979        PMID: 119827      PMCID: PMC2228576          DOI: 10.1085/jgp.74.6.713

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


  25 in total

1.  Effect of dopamine and haloperidol on the c-wave and light peak of light-induced retinal responses in chick eye.

Authors:  T Sato; T Yoneyama; H K Kim; T A Suzuki
Journal:  Doc Ophthalmol       Date:  1987-01       Impact factor: 2.379

2.  Is the potassium channel distribution in glial cells optimal for spatial buffering of potassium?

Authors:  H Brew; D Attwell
Journal:  Biophys J       Date:  1985-11       Impact factor: 4.033

3.  C-wave versus electrooculogram in diseases of the retinal pigment epithelium.

Authors:  J Röver; M Bach
Journal:  Doc Ophthalmol       Date:  1987-03       Impact factor: 2.379

Review 4.  Interactions between the retinal pigment epithelium and the neural retina.

Authors:  R H Steinberg
Journal:  Doc Ophthalmol       Date:  1985-10-15       Impact factor: 2.379

5.  Batrachotoxin uncouples gating charge immobilization from fast Na inactivation in squid giant axons.

Authors:  J Tanguy; J Z Yeh
Journal:  Biophys J       Date:  1988-10       Impact factor: 4.033

6.  Comparison between the slow cornea-negative PIII component of the ERG and potassium changes in the isolated rabbit retina.

Authors:  R Hanitzsch
Journal:  Doc Ophthalmol       Date:  1993       Impact factor: 2.379

7.  Effects of alpha-aminoadipic acid on the glutamate-isolated P III of the rabbit electroretinogram.

Authors:  A Reichenbach; F Wohlrab
Journal:  Doc Ophthalmol       Date:  1985-06-30       Impact factor: 2.379

8.  The C-wave in hereditary degenerations of the ocular fundus.

Authors:  J Röver; M Bach
Journal:  Doc Ophthalmol       Date:  1985-08-30       Impact factor: 2.379

9.  Electrophysiological consequences of retinal hypoxia.

Authors:  R A Linsenmeier
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1990       Impact factor: 3.117

10.  Potassium transport across the frog retinal pigment epithelium.

Authors:  S S Miller; R H Steinberg
Journal:  J Membr Biol       Date:  1982       Impact factor: 1.843

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