Development of the Electroretinographic Oscillatory Potentials in Normal and ROP Rats
To study the development of the electroretinographic (ERG) oscillatory potentials (OPs) in rats and to compare normal OPs with those in a rat model of retinopathy of prematurity (ROP). Following a longitudinal design, ERG responses to a greater than 5 log unit range of full-field stimuli were record...
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Veröffentlicht in: | Investigative ophthalmology & visual science 2006-12, Vol.47 (12), p.5447-5452 |
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creator | Liu, Kegao Akula, James D Hansen, Ronald M Moskowitz, Anne Kleinman, Michael S Fulton, Anne B |
description | To study the development of the electroretinographic (ERG) oscillatory potentials (OPs) in rats and to compare normal OPs with those in a rat model of retinopathy of prematurity (ROP).
Following a longitudinal design, ERG responses to a greater than 5 log unit range of full-field stimuli were recorded in dark-adapted rats at postnatal day (P) 18, P31, P47, and P67. The ERG records were digitally filtered (60-235 Hz), and the trough-to-peak amplitudes and implicit times of OP2, OP3, OP4, and OP5 were measured. Additionally, rats with oxygen-induced retinopathy, a model of ROP, were studied at P31.
Generally, OP amplitude increased and implicit time decreased with increasing stimulus intensity. The shape of the stimulus-response functions changed with age. The amplitudes of OP2, OP3, and OP4 were largest at P31. OP5 was largest at P47. All OPs were significantly affected in ROP rats; OP5 was least affected by ROP.
A prolonged normal course of OP development, which featured waxing and waning of amplitudes, was observed and might have been consequent to maturation and then to final refinements of inner retinal circuitry. In ROP rats, marked attenuation of early OPs was consistent with persistent dysfunction of photoreceptors, and significant attenuation of the late OP5 was evidence of compromised function of inner retinal circuitry. |
doi_str_mv | 10.1167/iovs.06-0702 |
format | Article |
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Following a longitudinal design, ERG responses to a greater than 5 log unit range of full-field stimuli were recorded in dark-adapted rats at postnatal day (P) 18, P31, P47, and P67. The ERG records were digitally filtered (60-235 Hz), and the trough-to-peak amplitudes and implicit times of OP2, OP3, OP4, and OP5 were measured. Additionally, rats with oxygen-induced retinopathy, a model of ROP, were studied at P31.
Generally, OP amplitude increased and implicit time decreased with increasing stimulus intensity. The shape of the stimulus-response functions changed with age. The amplitudes of OP2, OP3, and OP4 were largest at P31. OP5 was largest at P47. All OPs were significantly affected in ROP rats; OP5 was least affected by ROP.
A prolonged normal course of OP development, which featured waxing and waning of amplitudes, was observed and might have been consequent to maturation and then to final refinements of inner retinal circuitry. In ROP rats, marked attenuation of early OPs was consistent with persistent dysfunction of photoreceptors, and significant attenuation of the late OP5 was evidence of compromised function of inner retinal circuitry.</description><identifier>ISSN: 0146-0404</identifier><identifier>ISSN: 1552-5783</identifier><identifier>EISSN: 1552-5783</identifier><identifier>DOI: 10.1167/iovs.06-0702</identifier><identifier>PMID: 17122135</identifier><identifier>CODEN: IOVSDA</identifier><language>eng</language><publisher>Rockville, MD: ARVO</publisher><subject>Aging - physiology ; Animals ; Biological and medical sciences ; Dark Adaptation ; Disease Models, Animal ; Electroretinography ; Eye and associated structures. Visual pathways and centers. Vision ; Fundamental and applied biological sciences. Psychology ; Humans ; Infant, Newborn ; Medical sciences ; Ophthalmology ; Oscillometry ; Oxygen - toxicity ; Photoreceptor Cells, Vertebrate - physiology ; Rats ; Rats, Sprague-Dawley ; Retinal Ganglion Cells - physiology ; Retinopathies ; Retinopathy of Prematurity - physiopathology ; Vertebrates: nervous system and sense organs</subject><ispartof>Investigative ophthalmology & visual science, 2006-12, Vol.47 (12), p.5447-5452</ispartof><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c347t-51735fda00c2002c39d1e8aa9c5567234c2d0cb22ef12a2b30b9dac023fd9b6d3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18305693$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17122135$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Kegao</creatorcontrib><creatorcontrib>Akula, James D</creatorcontrib><creatorcontrib>Hansen, Ronald M</creatorcontrib><creatorcontrib>Moskowitz, Anne</creatorcontrib><creatorcontrib>Kleinman, Michael S</creatorcontrib><creatorcontrib>Fulton, Anne B</creatorcontrib><title>Development of the Electroretinographic Oscillatory Potentials in Normal and ROP Rats</title><title>Investigative ophthalmology & visual science</title><addtitle>Invest Ophthalmol Vis Sci</addtitle><description>To study the development of the electroretinographic (ERG) oscillatory potentials (OPs) in rats and to compare normal OPs with those in a rat model of retinopathy of prematurity (ROP).
Following a longitudinal design, ERG responses to a greater than 5 log unit range of full-field stimuli were recorded in dark-adapted rats at postnatal day (P) 18, P31, P47, and P67. The ERG records were digitally filtered (60-235 Hz), and the trough-to-peak amplitudes and implicit times of OP2, OP3, OP4, and OP5 were measured. Additionally, rats with oxygen-induced retinopathy, a model of ROP, were studied at P31.
Generally, OP amplitude increased and implicit time decreased with increasing stimulus intensity. The shape of the stimulus-response functions changed with age. The amplitudes of OP2, OP3, and OP4 were largest at P31. OP5 was largest at P47. All OPs were significantly affected in ROP rats; OP5 was least affected by ROP.
A prolonged normal course of OP development, which featured waxing and waning of amplitudes, was observed and might have been consequent to maturation and then to final refinements of inner retinal circuitry. In ROP rats, marked attenuation of early OPs was consistent with persistent dysfunction of photoreceptors, and significant attenuation of the late OP5 was evidence of compromised function of inner retinal circuitry.</description><subject>Aging - physiology</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Dark Adaptation</subject><subject>Disease Models, Animal</subject><subject>Electroretinography</subject><subject>Eye and associated structures. Visual pathways and centers. Vision</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Infant, Newborn</subject><subject>Medical sciences</subject><subject>Ophthalmology</subject><subject>Oscillometry</subject><subject>Oxygen - toxicity</subject><subject>Photoreceptor Cells, Vertebrate - physiology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Retinal Ganglion Cells - physiology</subject><subject>Retinopathies</subject><subject>Retinopathy of Prematurity - physiopathology</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0146-0404</issn><issn>1552-5783</issn><issn>1552-5783</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpF0M9rwjAUwPEwNqZzu-08chm7rO4laRp7HM79AJki8xzSNNWM2kjSWfzvF1HwFHj58Hh8EbonMCQkEy_W7cIQsgQE0AvUJ5zThIsRu0R9IGmcp5D20E0IvwCUEArXqEcEoZQw3kfLN7MztdtuTNNiV-F2bfCkNrr1zpvWNm7l1XZtNZ4Fbetatc7v8dy1kVtVB2wb_O38RtVYNSVezOZ4odpwi66q-GvuTu8ALd8nP-PPZDr7-Bq_ThPNUtEmnAjGq1IBaBqP0ywviRkplWvOM0FZqmkJuqDUVIQqWjAo8lJpoKwq8yIr2QA9H_dq70LwppJbbzfK7yUBeagjD3UkZPJQJ_KHI9_-FRtTnvEpRwSPJ6CCVnXlVaNtOLsRA57lLLqno1vb1bqz3sgQE9RxLZFd16VCEip5mgr2D_bye60</recordid><startdate>20061201</startdate><enddate>20061201</enddate><creator>Liu, Kegao</creator><creator>Akula, James D</creator><creator>Hansen, Ronald M</creator><creator>Moskowitz, Anne</creator><creator>Kleinman, Michael S</creator><creator>Fulton, Anne B</creator><general>ARVO</general><general>Association for Research in Vision and Ophtalmology</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20061201</creationdate><title>Development of the Electroretinographic Oscillatory Potentials in Normal and ROP Rats</title><author>Liu, Kegao ; Akula, James D ; Hansen, Ronald M ; Moskowitz, Anne ; Kleinman, Michael S ; Fulton, Anne B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c347t-51735fda00c2002c39d1e8aa9c5567234c2d0cb22ef12a2b30b9dac023fd9b6d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Aging - physiology</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Dark Adaptation</topic><topic>Disease Models, Animal</topic><topic>Electroretinography</topic><topic>Eye and associated structures. Visual pathways and centers. Vision</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>Infant, Newborn</topic><topic>Medical sciences</topic><topic>Ophthalmology</topic><topic>Oscillometry</topic><topic>Oxygen - toxicity</topic><topic>Photoreceptor Cells, Vertebrate - physiology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Retinal Ganglion Cells - physiology</topic><topic>Retinopathies</topic><topic>Retinopathy of Prematurity - physiopathology</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Kegao</creatorcontrib><creatorcontrib>Akula, James D</creatorcontrib><creatorcontrib>Hansen, Ronald M</creatorcontrib><creatorcontrib>Moskowitz, Anne</creatorcontrib><creatorcontrib>Kleinman, Michael S</creatorcontrib><creatorcontrib>Fulton, Anne B</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Investigative ophthalmology & visual science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Kegao</au><au>Akula, James D</au><au>Hansen, Ronald M</au><au>Moskowitz, Anne</au><au>Kleinman, Michael S</au><au>Fulton, Anne B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of the Electroretinographic Oscillatory Potentials in Normal and ROP Rats</atitle><jtitle>Investigative ophthalmology & visual science</jtitle><addtitle>Invest Ophthalmol Vis Sci</addtitle><date>2006-12-01</date><risdate>2006</risdate><volume>47</volume><issue>12</issue><spage>5447</spage><epage>5452</epage><pages>5447-5452</pages><issn>0146-0404</issn><issn>1552-5783</issn><eissn>1552-5783</eissn><coden>IOVSDA</coden><abstract>To study the development of the electroretinographic (ERG) oscillatory potentials (OPs) in rats and to compare normal OPs with those in a rat model of retinopathy of prematurity (ROP).
Following a longitudinal design, ERG responses to a greater than 5 log unit range of full-field stimuli were recorded in dark-adapted rats at postnatal day (P) 18, P31, P47, and P67. The ERG records were digitally filtered (60-235 Hz), and the trough-to-peak amplitudes and implicit times of OP2, OP3, OP4, and OP5 were measured. Additionally, rats with oxygen-induced retinopathy, a model of ROP, were studied at P31.
Generally, OP amplitude increased and implicit time decreased with increasing stimulus intensity. The shape of the stimulus-response functions changed with age. The amplitudes of OP2, OP3, and OP4 were largest at P31. OP5 was largest at P47. All OPs were significantly affected in ROP rats; OP5 was least affected by ROP.
A prolonged normal course of OP development, which featured waxing and waning of amplitudes, was observed and might have been consequent to maturation and then to final refinements of inner retinal circuitry. In ROP rats, marked attenuation of early OPs was consistent with persistent dysfunction of photoreceptors, and significant attenuation of the late OP5 was evidence of compromised function of inner retinal circuitry.</abstract><cop>Rockville, MD</cop><pub>ARVO</pub><pmid>17122135</pmid><doi>10.1167/iovs.06-0702</doi><tpages>6</tpages></addata></record> |
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subjects | Aging - physiology Animals Biological and medical sciences Dark Adaptation Disease Models, Animal Electroretinography Eye and associated structures. Visual pathways and centers. Vision Fundamental and applied biological sciences. Psychology Humans Infant, Newborn Medical sciences Ophthalmology Oscillometry Oxygen - toxicity Photoreceptor Cells, Vertebrate - physiology Rats Rats, Sprague-Dawley Retinal Ganglion Cells - physiology Retinopathies Retinopathy of Prematurity - physiopathology Vertebrates: nervous system and sense organs |
title | Development of the Electroretinographic Oscillatory Potentials in Normal and ROP Rats |
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