Cargando…

Degeneration Modulates Retinal Response to Transient Exogenous Oxidative Injury

PURPOSE: Oxidative injury is involved in retinal and macular degeneration. We aim to assess if retinal degeneration associated with genetic defect modulates the retinal threshold for encountering additional oxidative challenges. METHODS: Retinal oxidative injury was induced in degenerating retinas (...

Descripción completa

Detalles Bibliográficos
Autores principales: Lederman, Michal, Hagbi-Levi, Shira, Grunin, Michelle, Obolensky, Alexey, Berenshtein, Eduard, Banin, Eyal, Chevion, Mordechai, Chowers, Itay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3931611/
https://www.ncbi.nlm.nih.gov/pubmed/24586289
http://dx.doi.org/10.1371/journal.pone.0087751
_version_ 1782304678881525760
author Lederman, Michal
Hagbi-Levi, Shira
Grunin, Michelle
Obolensky, Alexey
Berenshtein, Eduard
Banin, Eyal
Chevion, Mordechai
Chowers, Itay
author_facet Lederman, Michal
Hagbi-Levi, Shira
Grunin, Michelle
Obolensky, Alexey
Berenshtein, Eduard
Banin, Eyal
Chevion, Mordechai
Chowers, Itay
author_sort Lederman, Michal
collection PubMed
description PURPOSE: Oxidative injury is involved in retinal and macular degeneration. We aim to assess if retinal degeneration associated with genetic defect modulates the retinal threshold for encountering additional oxidative challenges. METHODS: Retinal oxidative injury was induced in degenerating retinas (rd10) and in control mice (WT) by intravitreal injections of paraquat (PQ). Retinal function and structure was evaluated by electroretinogram (ERG) and histology, respectively. Oxidative injury was assessed by immunohistochemistry for 4-Hydroxy-2-nonenal (HNE), and by Thiobarbituric Acid Reactive Substances (TBARS) and protein carbonyl content (PCC) assays. Anti-oxidant mechanism was assessed by quantitative real time PCR (QPCR) for mRNA of antioxidant genes and genes related to iron metabolism, and by catalase activity assay. RESULTS: Three days following PQ injections (1 µl of 0.25, 0.75, and 2 mM) the average ERG amplitudes decreased more in the WT mice compared with the rd10 mice. For example, following 2 mM PQ injection, ERG amplitudes reduced 1.84-fold more in WT compared with rd10 mice (p = 0.02). Injection of 4 mM PQ resulted in retinal destruction. Altered retina morphology associated with PQ was substantially more severe in WT eyes compared with rd10 eyes. Oxidative injury according to HNE staining and TBARS assay increased 1.3-fold and 2.1-fold more, respectively, in WT compared with rd10 mice. At baseline, prior to PQ injection, mRNA levels of antioxidant genes (Superoxide Dismutase1, Glutathione Peroxidase1, Catalase) and of Transferrin measured by quantitative PCR were 2.1–7.8-fold higher in rd10 compared with WT mice (p<0.01 each), and catalase activity was 1.7-fold higher in rd10 (p = 0.0006). CONCLUSIONS: This data suggests that degenerating rd10 retinas encounter a relatively lower degree of damage in response to oxidative injury compared with normal retinas. Constitutive up-regulation of the oxidative defense mechanism in degenerating retinas may confer such relative protection from oxidative injury.
format Online
Article
Text
id pubmed-3931611
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-39316112014-02-25 Degeneration Modulates Retinal Response to Transient Exogenous Oxidative Injury Lederman, Michal Hagbi-Levi, Shira Grunin, Michelle Obolensky, Alexey Berenshtein, Eduard Banin, Eyal Chevion, Mordechai Chowers, Itay PLoS One Research Article PURPOSE: Oxidative injury is involved in retinal and macular degeneration. We aim to assess if retinal degeneration associated with genetic defect modulates the retinal threshold for encountering additional oxidative challenges. METHODS: Retinal oxidative injury was induced in degenerating retinas (rd10) and in control mice (WT) by intravitreal injections of paraquat (PQ). Retinal function and structure was evaluated by electroretinogram (ERG) and histology, respectively. Oxidative injury was assessed by immunohistochemistry for 4-Hydroxy-2-nonenal (HNE), and by Thiobarbituric Acid Reactive Substances (TBARS) and protein carbonyl content (PCC) assays. Anti-oxidant mechanism was assessed by quantitative real time PCR (QPCR) for mRNA of antioxidant genes and genes related to iron metabolism, and by catalase activity assay. RESULTS: Three days following PQ injections (1 µl of 0.25, 0.75, and 2 mM) the average ERG amplitudes decreased more in the WT mice compared with the rd10 mice. For example, following 2 mM PQ injection, ERG amplitudes reduced 1.84-fold more in WT compared with rd10 mice (p = 0.02). Injection of 4 mM PQ resulted in retinal destruction. Altered retina morphology associated with PQ was substantially more severe in WT eyes compared with rd10 eyes. Oxidative injury according to HNE staining and TBARS assay increased 1.3-fold and 2.1-fold more, respectively, in WT compared with rd10 mice. At baseline, prior to PQ injection, mRNA levels of antioxidant genes (Superoxide Dismutase1, Glutathione Peroxidase1, Catalase) and of Transferrin measured by quantitative PCR were 2.1–7.8-fold higher in rd10 compared with WT mice (p<0.01 each), and catalase activity was 1.7-fold higher in rd10 (p = 0.0006). CONCLUSIONS: This data suggests that degenerating rd10 retinas encounter a relatively lower degree of damage in response to oxidative injury compared with normal retinas. Constitutive up-regulation of the oxidative defense mechanism in degenerating retinas may confer such relative protection from oxidative injury. Public Library of Science 2014-02-21 /pmc/articles/PMC3931611/ /pubmed/24586289 http://dx.doi.org/10.1371/journal.pone.0087751 Text en © 2014 Lederman et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Lederman, Michal
Hagbi-Levi, Shira
Grunin, Michelle
Obolensky, Alexey
Berenshtein, Eduard
Banin, Eyal
Chevion, Mordechai
Chowers, Itay
Degeneration Modulates Retinal Response to Transient Exogenous Oxidative Injury
title Degeneration Modulates Retinal Response to Transient Exogenous Oxidative Injury
title_full Degeneration Modulates Retinal Response to Transient Exogenous Oxidative Injury
title_fullStr Degeneration Modulates Retinal Response to Transient Exogenous Oxidative Injury
title_full_unstemmed Degeneration Modulates Retinal Response to Transient Exogenous Oxidative Injury
title_short Degeneration Modulates Retinal Response to Transient Exogenous Oxidative Injury
title_sort degeneration modulates retinal response to transient exogenous oxidative injury
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3931611/
https://www.ncbi.nlm.nih.gov/pubmed/24586289
http://dx.doi.org/10.1371/journal.pone.0087751
work_keys_str_mv AT ledermanmichal degenerationmodulatesretinalresponsetotransientexogenousoxidativeinjury
AT hagbilevishira degenerationmodulatesretinalresponsetotransientexogenousoxidativeinjury
AT gruninmichelle degenerationmodulatesretinalresponsetotransientexogenousoxidativeinjury
AT obolenskyalexey degenerationmodulatesretinalresponsetotransientexogenousoxidativeinjury
AT berenshteineduard degenerationmodulatesretinalresponsetotransientexogenousoxidativeinjury
AT banineyal degenerationmodulatesretinalresponsetotransientexogenousoxidativeinjury
AT chevionmordechai degenerationmodulatesretinalresponsetotransientexogenousoxidativeinjury
AT chowersitay degenerationmodulatesretinalresponsetotransientexogenousoxidativeinjury