Literature DB >> 3744728

Mechanisms of hypoxic effects on the cat DC electroretinogram.

R A Linsenmeier, R H Steinberg.   

Abstract

Mild hypoxia elevates the standing potential and alters three slow components of the DC electroretinogram in the cat: the c-wave, the fast-oscillation trough, and the light peak. This paper considers the cellular mechanisms of these effects. Elevation of the standing potential results from a depolarization of the basal membrane of retinal pigment epithelial (RPE) cells. The depolarization is indirectly initiated by an elevation of [K+]0 in the subretinal space during hypoxia, and is accompanied by a decrease in basal membrane resistance that leads to an increase in the c-wave. There is also some evidence that hypoxia may alter the standing potential by directly affecting the basal membrane of the RPE. The fast-oscillation trough, which follows the c-wave when illumination is maintained, deepens during hypoxia. This is caused primarily by an increase in the amplitude of the delayed hyperpolarization of the RPE basal membrane that results from a slowing of the rate of recovery of light-evoked [K+]0 during hypoxia. The changes in [K+]0 probably result, in turn, from a decrease in the rate of the photoreceptors' Na+/K+ pump. The light peak's amplitude is reduced during hypoxia and its time-to-peak is lengthened, and this may be related to a change in photoreceptor metabolism that is distinct from the effect on the Na+/K+ pump. Knowledge of these mechanisms may eventually enhance the clinical usefulness of the standing potential and the c-wave, fast-oscillation, and light peak.

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Year:  1986        PMID: 3744728

Source DB:  PubMed          Journal:  Invest Ophthalmol Vis Sci        ISSN: 0146-0404            Impact factor:   4.799


  9 in total

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2.  Apical and basal membrane ion transport mechanisms in bovine retinal pigment epithelium.

Authors:  D P Joseph; S S Miller
Journal:  J Physiol       Date:  1991-04       Impact factor: 5.182

3.  The peak latency of the slow oscillation in EOG.

Authors:  M R Lessel; A Thaler; P Heilig
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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

Review 5.  Retinal oxygen: from animals to humans.

Authors:  Robert A Linsenmeier; Hao F Zhang
Journal:  Prog Retin Eye Res       Date:  2017-01-18       Impact factor: 21.198

6.  Electro-oculogram changes in patients with ocular hypertension and primary open-angle glaucoma.

Authors:  L Mehaffey; K Holopigian; W Seiple
Journal:  Doc Ophthalmol       Date:  1993       Impact factor: 2.379

7.  Electrophysiological consequences of retinal hypoxia.

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

8.  Oxygen distribution and consumption in the cat retina during normoxia and hypoxemia.

Authors:  R A Linsenmeier; R D Braun
Journal:  J Gen Physiol       Date:  1992-02       Impact factor: 4.086

9.  Role of the superior salivatory nucleus in parasympathetic control of choroidal blood flow and in maintenance of retinal health.

Authors:  Chunyan Li; Malinda E C Fitzgerald; Nobel Del Mar; Hongbing Wang; Corey Haughey; Marcia G Honig; Anton Reiner
Journal:  Exp Eye Res       Date:  2021-03-16       Impact factor: 3.467

  9 in total

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