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Cone ERG Changes During Light Adaptation in Two All-Cone Mutant Mice: Implications for Rod-Cone Pathway Interactions
PURPOSE: The b-wave of the cone ERG increases in amplitude and speed during the first few minutes of adaptation to a rod-suppressing background light. Earlier studies implicate rod pathway input to the cone pathway in these changes. METHODS: The timing and amplitude of the cone b-wave and isolated o...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Association for Research in Vision and Ophthalmology
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6716952/ https://www.ncbi.nlm.nih.gov/pubmed/31469895 http://dx.doi.org/10.1167/iovs.19-27242 |
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author | Bush, Ronald A. Tanikawa, Atsuhiro Zeng, Yong Sieving, Paul A. |
author_facet | Bush, Ronald A. Tanikawa, Atsuhiro Zeng, Yong Sieving, Paul A. |
author_sort | Bush, Ronald A. |
collection | PubMed |
description | PURPOSE: The b-wave of the cone ERG increases in amplitude and speed during the first few minutes of adaptation to a rod-suppressing background light. Earlier studies implicate rod pathway input to the cone pathway in these changes. METHODS: The timing and amplitude of the cone b-wave and isolated oscillatory potentials (OP) during the first 10 minutes of light adaptation in wild-type (WT) mice and two mutant lines without functional rods was examined: rhodopsin knockout (Rho(−/−)), lacking rod outer segments, and NRL knockout (Nrl(−/−)), in which rods are replaced by S-cones. Expression of the immediate-early gene c-fos, which is increased in the inner retina by light-induced activity, was evaluated by immunohistochemistry in dark- and light-adapted retinas. RESULTS: WT b-wave and OP amplitudes increased, and implicit times decreased during light adaptation. Subtracting OP did not alter b-wave changes. Rho(−/−) b-wave and OP amplitudes did not increase during adaptation. B-wave timing and amplitude and the timing of the major OP at 1 minute of adaptation were equivalent to WT at 10 minutes. The light-adapted ERG b-wave in Nrl(−/−) mice, which originates in both the rod and cone pathways, changed in absolute amplitude and timing similar to WT. C-fos expression was present in the inner retinas of dark-adapted Rho(−/−) but not WT or Nrl(−/−) mice. CONCLUSIONS: Activity in the distal rod pathway produces changes in the cone ERG during light adaptation. Rods in Rho(−/−) mice constitutively activate this rod-cone pathway interaction. The rod pathway S-cones in Nrl(−/−) mice may maintain the WT interaction. |
format | Online Article Text |
id | pubmed-6716952 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Association for Research in Vision and Ophthalmology |
record_format | MEDLINE/PubMed |
spelling | pubmed-67169522019-09-13 Cone ERG Changes During Light Adaptation in Two All-Cone Mutant Mice: Implications for Rod-Cone Pathway Interactions Bush, Ronald A. Tanikawa, Atsuhiro Zeng, Yong Sieving, Paul A. Invest Ophthalmol Vis Sci Retina PURPOSE: The b-wave of the cone ERG increases in amplitude and speed during the first few minutes of adaptation to a rod-suppressing background light. Earlier studies implicate rod pathway input to the cone pathway in these changes. METHODS: The timing and amplitude of the cone b-wave and isolated oscillatory potentials (OP) during the first 10 minutes of light adaptation in wild-type (WT) mice and two mutant lines without functional rods was examined: rhodopsin knockout (Rho(−/−)), lacking rod outer segments, and NRL knockout (Nrl(−/−)), in which rods are replaced by S-cones. Expression of the immediate-early gene c-fos, which is increased in the inner retina by light-induced activity, was evaluated by immunohistochemistry in dark- and light-adapted retinas. RESULTS: WT b-wave and OP amplitudes increased, and implicit times decreased during light adaptation. Subtracting OP did not alter b-wave changes. Rho(−/−) b-wave and OP amplitudes did not increase during adaptation. B-wave timing and amplitude and the timing of the major OP at 1 minute of adaptation were equivalent to WT at 10 minutes. The light-adapted ERG b-wave in Nrl(−/−) mice, which originates in both the rod and cone pathways, changed in absolute amplitude and timing similar to WT. C-fos expression was present in the inner retinas of dark-adapted Rho(−/−) but not WT or Nrl(−/−) mice. CONCLUSIONS: Activity in the distal rod pathway produces changes in the cone ERG during light adaptation. Rods in Rho(−/−) mice constitutively activate this rod-cone pathway interaction. The rod pathway S-cones in Nrl(−/−) mice may maintain the WT interaction. The Association for Research in Vision and Ophthalmology 2019-08 /pmc/articles/PMC6716952/ /pubmed/31469895 http://dx.doi.org/10.1167/iovs.19-27242 Text en Copyright 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. |
spellingShingle | Retina Bush, Ronald A. Tanikawa, Atsuhiro Zeng, Yong Sieving, Paul A. Cone ERG Changes During Light Adaptation in Two All-Cone Mutant Mice: Implications for Rod-Cone Pathway Interactions |
title | Cone ERG Changes During Light Adaptation in Two All-Cone Mutant Mice: Implications for Rod-Cone Pathway Interactions |
title_full | Cone ERG Changes During Light Adaptation in Two All-Cone Mutant Mice: Implications for Rod-Cone Pathway Interactions |
title_fullStr | Cone ERG Changes During Light Adaptation in Two All-Cone Mutant Mice: Implications for Rod-Cone Pathway Interactions |
title_full_unstemmed | Cone ERG Changes During Light Adaptation in Two All-Cone Mutant Mice: Implications for Rod-Cone Pathway Interactions |
title_short | Cone ERG Changes During Light Adaptation in Two All-Cone Mutant Mice: Implications for Rod-Cone Pathway Interactions |
title_sort | cone erg changes during light adaptation in two all-cone mutant mice: implications for rod-cone pathway interactions |
topic | Retina |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6716952/ https://www.ncbi.nlm.nih.gov/pubmed/31469895 http://dx.doi.org/10.1167/iovs.19-27242 |
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