Literature DB >> 7153919

Origin of the light peak: in vitro study of Gekko gekko.

E R Griff, R H Steinberg.   

Abstract

1. The light peak is a large, light-evoked increase in standing potential recorded in mammals, birds and reptiles. We have studied the cellular origin of the light peak in an in vitro preparation of neural retina-pigment epithelium (r.p.e)-choroid from the lizard, Gekko gekko. The tissue was mounted between two separate bathing solutions; the trans-tissue potential was recorded retinal-side positive; micro-electrodes were introduced to measure the trans-epithelial potential (t.e.p.) and to record intracellularly from the r.p.e.2. A 10 min stimulus of diffuse white light evoked an increase in trans-tissue potential that reached maximum amplitude, the light peak, about 15 min after stimulus onset. Since the light peak is present in vitro, it must originate in either the neural retina or the r.p.e.3. A micro-electrode was positioned in the subretinal space and the trans-retinal potential and t.e.p. were measured simultaneously. A 10 min stimulus produced an increase in t.e.p. equal in magnitude and time course to the trans-tissue light peak; no potential was present across the retina. The light peak is therefore generated solely across the r.p.e.4. Intracellular r.p.e. recordings were made to determine whether the light peak was generated at the apical or basal membrane or across the paracellular shunt. A 10 min stimulus first caused a hyperpolarization of both membranes with a time course similar to the r.p.e. c-wave followed by a depolarization of both membranes with the time course of the light peak. We conclude that whereas the r.p.e. c-wave results from a hyperpolarization of the apical membrane, the light peak is generated by a depolarization of the basal membrane of the r.p.e.5. Changes in tissue resistance, R(t), and the ratio of apical to basal membrane resistances, a, were monitored during the light peak by passing current across the tissue and measuring the appropriate current-induced voltages. R(t) decreased and a increased with the time course of the light peak. Assuming that the paracellular shunt resistance is constant, we conclude that the light peak is accompanied by an increase in basal membrane conductance.6. This and the following paper present the first direct demonstration of an interaction between the neural retina and the basal membrane of the r.p.e. The light peak, initiated by absorption of light by photoreceptors, results in a depolarization and conductance increase of the basal membrane.

Entities:  

Mesh:

Year:  1982        PMID: 7153919      PMCID: PMC1197772          DOI: 10.1113/jphysiol.1982.sp014395

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


  23 in total

1.  Correlation of light-induced changes in retinal extracellular potassium concentration with c-wave of the electroretinogram.

Authors:  B Oakley; D G Green
Journal:  J Neurophysiol       Date:  1976-09       Impact factor: 2.714

2.  The directly recorded standing potential of the human eye.

Authors:  K O Skoog
Journal:  Acta Ophthalmol (Copenh)       Date:  1975-03

3.  Instrumentation and technique for beveling fine micropipette electrodes.

Authors:  K T Brown; D G Flaming
Journal:  Brain Res       Date:  1975-03-14       Impact factor: 3.252

4.  The slow oscillation of the retinal potential: a biochemical feedback stimulated by the activity of rods and cones.

Authors:  R Täumer; N Rohde; D Pernice
Journal:  Bibl Ophthalmol       Date:  1976

5.  Further investigations concerning the fast oscillation of the retinal potential.

Authors:  R Täumer; J Hennig; L Wolff
Journal:  Bibl Ophthalmol       Date:  1976

6.  The in vitro frog pigment epithelial cell hyperpolarization in response to light.

Authors:  B Oakley; R H Steinberg; S S Miller; S E Nilsson
Journal:  Invest Ophthalmol Vis Sci       Date:  1977-08       Impact factor: 4.799

7.  The intercellular junctional complexes of retinal pigment epithelia.

Authors:  A J Hudspeth; A G Yee
Journal:  Invest Ophthalmol       Date:  1973-05

8.  Route of passive ion permeation in epithelia.

Authors:  E Frömter; J Diamond
Journal:  Nat New Biol       Date:  1972-01-05

9.  Components of the electroretinogram--a reappraisal.

Authors:  R W Rodieck
Journal:  Vision Res       Date:  1972-05       Impact factor: 1.886

10.  Variations in the corneo-retinal standing potential of the vertebrate eye during light and dark adaptations.

Authors:  N Kikawada
Journal:  Jpn J Physiol       Date:  1968-12-15
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  26 in total

1.  A simple and stable d.c.electrode for ocular electrophysiology.

Authors:  G Niemeyer; N Kueng
Journal:  Doc Ophthalmol       Date:  1998       Impact factor: 2.379

2.  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

3.  EOG and ERG modifications induced in the chicken eye after blockade of catecholamine and 5-hydroxytryptamine biosynthesis.

Authors:  G Rudolf; N Wioland; E Kempf; N Bonaventure
Journal:  Doc Ophthalmol       Date:  1990-11       Impact factor: 2.379

4.  Effects of intraocular irrigation with melatonin on the c-wave of the direct current electroretinogram and on the standing potential of the eye in albino rabbits.

Authors:  O Textorius; S E Nilsson
Journal:  Doc Ophthalmol       Date:  1987-01       Impact factor: 2.379

5.  Concentration-dependent effects of dopamine on the direct current electroretinogram of pigmented rabbits during prolonged intermittent recording.

Authors:  Eva Gottvall; Ola Textorius
Journal:  Doc Ophthalmol       Date:  2003-03       Impact factor: 2.379

6.  Long-term behavior and intra-individual stability of the direct current electroretinogram and of the standing potential in the albino rabbit eye.

Authors:  Eva Gottvall; Ola Textorius
Journal:  Doc Ophthalmol       Date:  2003-03       Impact factor: 2.379

7.  Incomplete congenital stationary night blindness: electroretinogram c-wave and electrooculogram light rise.

Authors:  Y Takahashi; S Onoe; N Asamizu; T Mori; Y Yoshimura; Y Tazawa
Journal:  Doc Ophthalmol       Date:  1988-09       Impact factor: 2.379

8.  Calcium blocks selectively the EOG-light peak.

Authors:  H Hofmann; G Niemeyer
Journal:  Doc Ophthalmol       Date:  1985-10-15       Impact factor: 2.379

9.  From sea lemons to c-waves.

Authors:  M F Marmor
Journal:  Cell Mol Neurobiol       Date:  1983-12       Impact factor: 5.046

10.  Combined photic and nonphotic electro-oculographic responses in the clinical evaluation of the retinal pigment epithelium.

Authors:  T Mori; M F Marmor; K Miyoshi; Y Tazawa
Journal:  Doc Ophthalmol       Date:  1991       Impact factor: 2.379

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