JN AJP: Heart and Circulatory Physiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 61: 1221-1232, 1989;
0022-3077/89 $5.00
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Frishman, L. J.
Right arrow Articles by Steinberg, R. H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Frishman, L. J.
Right arrow Articles by Steinberg, R. H.

Journal of Neurophysiology, Vol 61, Issue 6 1221-1232, Copyright © 1989 by APS


ARTICLES

Intraretinal analysis of the threshold dark-adapted ERG of cat retina

L. J. Frishman and R. H. Steinberg
Department of Physiology, University of California, San Francisco 94143.

1. The dark-adapted electroretinogram (ERG) obtained with 4-s flashes near threshold and at low intensities has three clear negative components: 1) a fast negative response at stimulus onset, 2) a slow negative response that increases in amplitude for about 2 s, and 3) a negative-going OFF response. The fast negative response was previously shown to originate from the scotopic threshold response (STR) arising in the proximal portion of neural retina. We investigated the intraretinal origins of the other two negative components and found that they also have origins in neural retina proximal to the photoreceptors. 2. In this study the ERG evoked in response to diffuse illumination of the dark-adapted cat retina was recorded between a chlorided silver wire in the vitreous and a plate behind the eye. Extracellular field potentials were recorded simultaneously with a microelectrode placed intraretinally at different retinal depths. In some cases light-dependent changes in extracellular K+ concentration ([K+]o) were recorded with the K+-selective barrel of a double-barreled microelectrode. 3. The three negative-going ERG potentials increased in amplitude from threshold up to approximately 6.0 log q.deg-2.s-1. The potential during illumination then became nearly flat, and the negative OFF response was exaggerated. At higher intensities, positive-going PII (DC-component and b-wave) and the c-wave emerged, whereas the a-wave (negative-going) was usually below threshold. 4. The slow negative ERG response was generated in neural retina, rather than by the retinal pigment epithelium. The response was positive-going in the transretinal recordings obtained in subretinal space. It was not, however, related to two positive-going responses from distal retina previously described as contributing negative components to the ERG: the neural retina component of the c-wave, termed slow PIII, and the rod-receptor potential. The slow negative response had a slower time course and lower threshold than slow PIII, and, more importantly, it was present in the absence of the [K+]o decrease in subretinal space that causes slow PIII. Furthermore, APB (1.2 mM vitreal concentration) blocked the entire negative-going ERG, whereas at higher intensities it blocked PII but not the c-wave in the ERG or slow PIII in transretinal recordings. These results indicate that the negative-going ERG components near threshold and at low intensities all originated proximal to the photoreceptors.(ABSTRACT TRUNCATED AT 400 WORDS)


This article has been cited by other articles:


Home page
IOVSHome page
S. Machida, D. Raz-Prag, R. N. Fariss, P. A. Sieving, and R. A. Bush
Photopic ERG Negative Response from Amacrine Cell Signaling in RCS Rat Retinal Degeneration
Invest. Ophthalmol. Vis. Sci., January 1, 2008; 49(1): 442 - 452.
[Abstract] [Full Text] [PDF]


Home page
IOVSHome page
B. Fortune, B. V. Bui, J. C. Morrison, E. C. Johnson, J. Dong, W. O. Cepurna, L. Jia, S. Barber, and G. A. Cioffi
Selective Ganglion Cell Functional Loss in Rats with Experimental Glaucoma
Invest. Ophthalmol. Vis. Sci., June 1, 2004; 45(6): 1854 - 1862.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
B. V. Bui and B. Fortune
Ganglion cell contributions to the rat full-field electroretinogram
J. Physiol., February 15, 2004; 555(1): 153 - 173.
[Abstract] [Full Text] [PDF]


Home page
IOVSHome page
S. Viswanathan, L. J. Frishman, J. G. Robson, and J. W. Walters
The Photopic Negative Response of the Flash Electroretinogram in Primary Open Angle Glaucoma
Invest. Ophthalmol. Vis. Sci., February 1, 2001; 42(2): 514 - 522.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online