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Rod and Cone Coupling Modulates Photopic ERG Responses in the Mouse Retina

Light adaptation changes both the sensitivity and maximum amplitude (R(max)) of the mouse photopic electroretinogram (ERG) b-wave. Using the ERG, we examined how modulation of gap junctional coupling between rod and cones alters the light-adapted ERG. To measure changes, a b-wave light adaptation en...

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Autores principales: Li, Yichao, Cohen, Ethan D., Qian, Haohua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7546330/
https://www.ncbi.nlm.nih.gov/pubmed/33100974
http://dx.doi.org/10.3389/fncel.2020.566712
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author Li, Yichao
Cohen, Ethan D.
Qian, Haohua
author_facet Li, Yichao
Cohen, Ethan D.
Qian, Haohua
author_sort Li, Yichao
collection PubMed
description Light adaptation changes both the sensitivity and maximum amplitude (R(max)) of the mouse photopic electroretinogram (ERG) b-wave. Using the ERG, we examined how modulation of gap junctional coupling between rod and cones alters the light-adapted ERG. To measure changes, a b-wave light adaptation enhancement factor (LAEF), was defined as the ratio of R(max) after 15 min light adaptation to R(max) recorded at the onset of an adapting light. For wild-type mice (WT), the LAEF averaged 2.64 ± 0.29, however, it was significantly reduced (1.06 ± 0.04) for connexin 36 knock out (Cx36KO) mice, which lack electrical coupling between photoreceptors. Wild type mice intraocularly injected with meclofenamic acid (MFA), a gap junction blocker, also showed a significantly reduced LAEF. Degeneration of rod photoreceptors significantly alters the effects of light adaptation on the photopic ERG response. Rd10 mice at P21, with large portions of their rod photoreceptors present in the retina, exhibited a similar b-wave enhancement as wildtype controls, with a LAEF of 2.55 ± 0.19. However, by P31 with most of their rod photoreceptors degenerated, rd10 mice had a much reduced b-wave enhancement during light-adaptation (LAEF of 1.54 ± 0.12). Flicker ERG responses showed a higher temporal amplitude in mesopic conditions for WT than those of Cx36KO mice, suggesting rod-cone coupling help high-frequency signals to pass from rods to cone pathways in the retina. In conclusion, our study provides a novel method to noninvasively measure the dynamics and modulation by the light adaptation for rod-cone gap junctional coupling in intact eyes.
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spelling pubmed-75463302020-10-22 Rod and Cone Coupling Modulates Photopic ERG Responses in the Mouse Retina Li, Yichao Cohen, Ethan D. Qian, Haohua Front Cell Neurosci Cellular Neuroscience Light adaptation changes both the sensitivity and maximum amplitude (R(max)) of the mouse photopic electroretinogram (ERG) b-wave. Using the ERG, we examined how modulation of gap junctional coupling between rod and cones alters the light-adapted ERG. To measure changes, a b-wave light adaptation enhancement factor (LAEF), was defined as the ratio of R(max) after 15 min light adaptation to R(max) recorded at the onset of an adapting light. For wild-type mice (WT), the LAEF averaged 2.64 ± 0.29, however, it was significantly reduced (1.06 ± 0.04) for connexin 36 knock out (Cx36KO) mice, which lack electrical coupling between photoreceptors. Wild type mice intraocularly injected with meclofenamic acid (MFA), a gap junction blocker, also showed a significantly reduced LAEF. Degeneration of rod photoreceptors significantly alters the effects of light adaptation on the photopic ERG response. Rd10 mice at P21, with large portions of their rod photoreceptors present in the retina, exhibited a similar b-wave enhancement as wildtype controls, with a LAEF of 2.55 ± 0.19. However, by P31 with most of their rod photoreceptors degenerated, rd10 mice had a much reduced b-wave enhancement during light-adaptation (LAEF of 1.54 ± 0.12). Flicker ERG responses showed a higher temporal amplitude in mesopic conditions for WT than those of Cx36KO mice, suggesting rod-cone coupling help high-frequency signals to pass from rods to cone pathways in the retina. In conclusion, our study provides a novel method to noninvasively measure the dynamics and modulation by the light adaptation for rod-cone gap junctional coupling in intact eyes. Frontiers Media S.A. 2020-09-25 /pmc/articles/PMC7546330/ /pubmed/33100974 http://dx.doi.org/10.3389/fncel.2020.566712 Text en Copyright © 2020 Li, Cohen and Qian. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular Neuroscience
Li, Yichao
Cohen, Ethan D.
Qian, Haohua
Rod and Cone Coupling Modulates Photopic ERG Responses in the Mouse Retina
title Rod and Cone Coupling Modulates Photopic ERG Responses in the Mouse Retina
title_full Rod and Cone Coupling Modulates Photopic ERG Responses in the Mouse Retina
title_fullStr Rod and Cone Coupling Modulates Photopic ERG Responses in the Mouse Retina
title_full_unstemmed Rod and Cone Coupling Modulates Photopic ERG Responses in the Mouse Retina
title_short Rod and Cone Coupling Modulates Photopic ERG Responses in the Mouse Retina
title_sort rod and cone coupling modulates photopic erg responses in the mouse retina
topic Cellular Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7546330/
https://www.ncbi.nlm.nih.gov/pubmed/33100974
http://dx.doi.org/10.3389/fncel.2020.566712
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