Literature DB >> 5571953

Rod-dependent intracellular responses to light recorded from the pigment epithelium of the cat retina.

R Schmidt, R H Steinberg.   

Abstract

1. Intracellular recordings from pigment epithelial cells reveal rod-dependent hyperpolarizing responses to light which are identical with the c-wave of the electroretinogram. These responses were studied as a function of the duration, intensity and area of light flashes and also were compared with rod-dependent horizontal cell responses recorded under similar conditions.2. Because of the long time constant of the response (800 msec), pigment epithelial responses increased in amplitude as flash duration was increased over a wide range. The response reached a plateau at a flash duration of 2.4 sec so that longer flashes only increased the duration of the response. Responses to repetitive flashes, even at a slow rate of 2/sec were integrated to produce a sustained voltage.3. The growth of pigment epithelial response amplitude as a function of flash duration could be divided into two components. The increase in amplitude as flash duration was increased from 5-50 msec was also observed in horizontal cells and was assumed to have originated in the rods. The growth in amplitude with longer flashes was unique to the pigment epithelial response.4. The pigment epithelial response increased in amplitude as spot size was increased, reaching 90% of maximum with an 0.36 mm diameter spot. A precise measurement of the receptive field could not be obtained, because the responses were recorded in the tapetal area of dark-adapted retinas. The b-wave of the local electroretinogram which was ;picked-up' intracellularly exhibited a much greater area effect.5. Pigment epithelial responses increased in amplitude as flash intensity was increased but the amplitude-log intensity functions differed as a function of flash duration. With long flashes (> 2.4 sec) the growth in amplitude was a power function of intensity (exponent = 0.6-0.7) and the response reached an amplitude ceiling at about 3.0 log td scotopic. At higher intensities the responses increased in duration (the rod after-effect). With short flashes, e.g. 480 msec, the responses continued to increase in amplitude with flash intensity well above the intensity needed to produce amplitude-ceilings for rod-dependent responses. This additional increase in amplitude resulted from integration of the rod after-effect by the pigment epithelial response.6. Rod-dependent horizontal cell responses followed the amplitude-log intensity functions that were recorded in pigment epithelial cells with long flashes. The rod after-effect was also the same function of log intensity in both responses.7. It was concluded that the pigment epithelial response is not generated by a late photoproduct. Rather, it appears to depend upon the same mechanism of rod excitation as the horizontal cell response, and the essential characteristics of both rod-dependent responses originate in individual rods.

Mesh:

Substances:

Year:  1971        PMID: 5571953      PMCID: PMC1331545          DOI: 10.1113/jphysiol.1971.sp009560

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


  24 in total

1.  Localization of origins of electroretinogram components by intraretinal recording in the intact cat eye.

Authors:  K T BROWN; T N WIESEL
Journal:  J Physiol       Date:  1961-09       Impact factor: 5.182

2.  Chemistry of visual adaptation in the rat.

Authors:  J E DOWLING
Journal:  Nature       Date:  1960-10-08       Impact factor: 49.962

3.  OPTICAL STIMULATOR, MICROELECTRODE ADVANCER, AND ASSOCIATED EQUIPMENT FOR INTRARETINAL NEUROPHYSIOLOGY IN CLOSED MAMMALIAN EYES.

Authors:  K T BROWN
Journal:  J Opt Soc Am       Date:  1964-01

4.  Signal transmission along retinal rods and the origin of the electroretinographic a-wave.

Authors:  R D Penn; W A Hagins
Journal:  Nature       Date:  1969-07-12       Impact factor: 49.962

5.  Delayed decay of the late receptor potential of monkey cones as a function of stimulus intensity.

Authors:  K T Brown; M Murakami
Journal:  Vision Res       Date:  1967-03       Impact factor: 1.886

6.  Rod-cone interaction in S-potentials from the cat retina.

Authors:  R H Steinberg
Journal:  Vision Res       Date:  1969-11       Impact factor: 1.886

7.  Rod and cone contributions to S-potentials from the cat retina.

Authors:  R H Steinberg
Journal:  Vision Res       Date:  1969-11       Impact factor: 1.886

8.  Comparison of the intraretinal b-wave and d.c. component in the area centralis of cat retina.

Authors:  R H Steinberg
Journal:  Vision Res       Date:  1969-03       Impact factor: 1.886

9.  Organization of the retina of the mudpuppy, Necturus maculosus. II. Intracellular recording.

Authors:  F S Werblin; J E Dowling
Journal:  J Neurophysiol       Date:  1969-05       Impact factor: 2.714

10.  Participation of the retinal pigment epithelium in the rod outer segment renewal process.

Authors:  R W Young; D Bok
Journal:  J Cell Biol       Date:  1969-08       Impact factor: 10.539

View more
  15 in total

Review 1.  The function of the retina in the perfused eye.

Authors:  G Niemeyer
Journal:  Doc Ophthalmol       Date:  1975-11-21       Impact factor: 2.379

2.  Light-evoked responses of the retinal pigment epithelium: changes accompanying photoreceptor loss in the mouse.

Authors:  Ivy S Samuels; Gwen M Sturgill; Gregory H Grossman; Mary E Rayborn; Joe G Hollyfield; Neal S Peachey
Journal:  J Neurophysiol       Date:  2010-05-19       Impact factor: 2.714

3.  Incremental responses to light recorded from pigment epithelial cells and horizontal cells of the cat retina.

Authors:  R H Steinberg
Journal:  J Physiol       Date:  1971-08       Impact factor: 5.182

4.  Osmotic pressure of the interstitial fluid obtained from neonatal chick eyes and its variation under light and dark adaptation.

Authors:  T Sato; T Yoneyama; N Matsumoto; K Somei; T A Suzuki; Y Tazawa
Journal:  Doc Ophthalmol       Date:  1985-10-30       Impact factor: 2.379

5.  Origin and sensitivity of the light peak in the intact cat eye.

Authors:  R A Linsenmeier; R H Steinberg
Journal:  J Physiol       Date:  1982-10       Impact factor: 5.182

6.  Metabolic responses to light in monkey photoreceptors.

Authors:  Shufan Wang; Gülnur Birol; Ewa Budzynski; Robert Flynn; Robert A Linsenmeier
Journal:  Curr Eye Res       Date:  2010-06       Impact factor: 2.424

7.  Combined effects of DL-alpha-aminoadipic acid with sodium iodate, ethyl alcohol, or light stimulation on the ERG c-wave and on the standing potential of albino rabbit eyes.

Authors:  O Textorius; E Welinder; S E Nilsson
Journal:  Doc Ophthalmol       Date:  1985-10-15       Impact factor: 2.379

8.  Exclusion of aldose reductase as a mediator of ERG deficits in a mouse model of diabetic eye disease.

Authors:  Ivy S Samuels; Chieh-Allen Lee; J Mark Petrash; Neal S Peachey; Timothy S Kern
Journal:  Vis Neurosci       Date:  2012-10-29       Impact factor: 3.241

9.  Light adaptation and temperature effects in rat PIII retinal response: analysis with a two-state model.

Authors:  J G Gale; T P Williams
Journal:  Proc Natl Acad Sci U S A       Date:  1980-07       Impact factor: 11.205

10.  Delayed basal hyperpolarization of cat retinal pigment epithelium and its relation to the fast oscillation of the DC electroretinogram.

Authors:  R A Linsenmeier; R H Steinberg
Journal:  J Gen Physiol       Date:  1984-02       Impact factor: 4.086

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.