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Loss of Daylight Vision in Retinal Degeneration: Are Oxidative Stress and Metabolic Dysregulation to Blame?
Retinitis pigmentosa is characterized by loss of night vision, followed by complete blindness. Over 40 genetic loci for retinitis pigmentosa have been identified in humans, primarily affecting photoreceptor structure and function. The availability of excellent animal models allows for a mechanistic...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Biochemistry and Molecular Biology
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3265845/ https://www.ncbi.nlm.nih.gov/pubmed/22074929 http://dx.doi.org/10.1074/jbc.R111.304428 |
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author | Punzo, Claudio Xiong, Wenjun Cepko, Constance L. |
author_facet | Punzo, Claudio Xiong, Wenjun Cepko, Constance L. |
author_sort | Punzo, Claudio |
collection | PubMed |
description | Retinitis pigmentosa is characterized by loss of night vision, followed by complete blindness. Over 40 genetic loci for retinitis pigmentosa have been identified in humans, primarily affecting photoreceptor structure and function. The availability of excellent animal models allows for a mechanistic characterization of the disease. Metabolic dysregulation and oxidative stress have been found to correlate with the loss of vision, particularly in cones, the type of photoreceptors that mediate daylight and color vision. The evidence that these problems actually cause loss of vision and potential therapeutic approaches targeting them are discussed. |
format | Online Article Text |
id | pubmed-3265845 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | American Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-32658452012-01-27 Loss of Daylight Vision in Retinal Degeneration: Are Oxidative Stress and Metabolic Dysregulation to Blame? Punzo, Claudio Xiong, Wenjun Cepko, Constance L. J Biol Chem Minireviews Retinitis pigmentosa is characterized by loss of night vision, followed by complete blindness. Over 40 genetic loci for retinitis pigmentosa have been identified in humans, primarily affecting photoreceptor structure and function. The availability of excellent animal models allows for a mechanistic characterization of the disease. Metabolic dysregulation and oxidative stress have been found to correlate with the loss of vision, particularly in cones, the type of photoreceptors that mediate daylight and color vision. The evidence that these problems actually cause loss of vision and potential therapeutic approaches targeting them are discussed. American Society for Biochemistry and Molecular Biology 2012-01-13 2011-11-10 /pmc/articles/PMC3265845/ /pubmed/22074929 http://dx.doi.org/10.1074/jbc.R111.304428 Text en © 2012 by The American Society for Biochemistry and Molecular Biology, Inc. Author's Choice—Final version full access. Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) applies to Author Choice Articles |
spellingShingle | Minireviews Punzo, Claudio Xiong, Wenjun Cepko, Constance L. Loss of Daylight Vision in Retinal Degeneration: Are Oxidative Stress and Metabolic Dysregulation to Blame? |
title | Loss of Daylight Vision in Retinal Degeneration: Are Oxidative Stress and Metabolic Dysregulation to Blame? |
title_full | Loss of Daylight Vision in Retinal Degeneration: Are Oxidative Stress and Metabolic Dysregulation to Blame? |
title_fullStr | Loss of Daylight Vision in Retinal Degeneration: Are Oxidative Stress and Metabolic Dysregulation to Blame? |
title_full_unstemmed | Loss of Daylight Vision in Retinal Degeneration: Are Oxidative Stress and Metabolic Dysregulation to Blame? |
title_short | Loss of Daylight Vision in Retinal Degeneration: Are Oxidative Stress and Metabolic Dysregulation to Blame? |
title_sort | loss of daylight vision in retinal degeneration: are oxidative stress and metabolic dysregulation to blame? |
topic | Minireviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3265845/ https://www.ncbi.nlm.nih.gov/pubmed/22074929 http://dx.doi.org/10.1074/jbc.R111.304428 |
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