High resolution imaging of fluorescein patterns in RCS rat retinae and their direct correlation with histology
To assess the progressive changes in the retinal vascular bed of dystrophic and non-dystrophic Royal College of Surgeons (RCS) rats, retinae, were visualised correlating in vivo fundus fluorescein angiography (FA) with histology. FA was performed in rats aged 5 weeks to 2 years, using a Zeiss confoc...
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Veröffentlicht in: | Experimental eye research 2006, Vol.82 (1), p.164-171 |
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creator | Zambarakji, H.J. Keegan, D.J. Holmes, T.M. Halfyard, A.S. Villegas-Perez, M.P. Charteris, D.G. Fitzke, F.W. Greenwood, J. Lund, R.D. |
description | To assess the progressive changes in the retinal vascular bed of dystrophic and non-dystrophic Royal College of Surgeons (RCS) rats, retinae, were visualised correlating in vivo fundus fluorescein angiography (FA) with histology.
FA was performed in rats aged 5 weeks to 2 years, using a Zeiss confocal scanning laser ophthalmoscope (cSLO). After the final imaging session, a subset of retinae were prepared for flat-mount histology and the vascular bed was visualised using nicotinamide adenine dinucleotide phosphate-diaphorase (NADPH-d) staining. While non-dystrophic rat retinae showed no substantive changes in vascular patterns with age and no demonstrable fluorescein leakage up to at least 1 year, dystrophic rat retinae showed abnormal vascular formations, demonstrable on FA and NADPH-d staining, which could be correlated in single retinae. Hyperfluorescent spots and late angiographic leakage were evident beginning at 10 weeks and progressed in severity with time: they were coincident in distribution with abnormal histological vascular complexes.
The ability to monitor the same retina serially makes this approach a valuable tool for studying the dynamics of vascular change in the diseased retina, not only during the course of degeneration but also when assessing efficacy of potential therapeutic approaches. |
doi_str_mv | 10.1016/j.exer.2005.06.006 |
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FA was performed in rats aged 5 weeks to 2 years, using a Zeiss confocal scanning laser ophthalmoscope (cSLO). After the final imaging session, a subset of retinae were prepared for flat-mount histology and the vascular bed was visualised using nicotinamide adenine dinucleotide phosphate-diaphorase (NADPH-d) staining. While non-dystrophic rat retinae showed no substantive changes in vascular patterns with age and no demonstrable fluorescein leakage up to at least 1 year, dystrophic rat retinae showed abnormal vascular formations, demonstrable on FA and NADPH-d staining, which could be correlated in single retinae. Hyperfluorescent spots and late angiographic leakage were evident beginning at 10 weeks and progressed in severity with time: they were coincident in distribution with abnormal histological vascular complexes.
The ability to monitor the same retina serially makes this approach a valuable tool for studying the dynamics of vascular change in the diseased retina, not only during the course of degeneration but also when assessing efficacy of potential therapeutic approaches.</description><identifier>ISSN: 0014-4835</identifier><identifier>EISSN: 1096-0007</identifier><identifier>DOI: 10.1016/j.exer.2005.06.006</identifier><identifier>PMID: 16054136</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Animals ; confocal scanning ophthalmoscope ; Disease Progression ; Fluorescein Angiography ; Microscopy, Confocal ; Muscular Dystrophies - pathology ; Rats ; Rats, Mutant Strains ; RCS rats ; retina ; Retina - pathology ; Retinal Degeneration - pathology ; Retinal Ganglion Cells - pathology ; Retinal Vessels - pathology ; vascular</subject><ispartof>Experimental eye research, 2006, Vol.82 (1), p.164-171</ispartof><rights>2005 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c354t-adab92a62df400ff09b7d3ba0df30bfec4bbb013561659c3449f9a1887547083</citedby><cites>FETCH-LOGICAL-c354t-adab92a62df400ff09b7d3ba0df30bfec4bbb013561659c3449f9a1887547083</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0014483505001806$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,4010,27900,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16054136$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zambarakji, H.J.</creatorcontrib><creatorcontrib>Keegan, D.J.</creatorcontrib><creatorcontrib>Holmes, T.M.</creatorcontrib><creatorcontrib>Halfyard, A.S.</creatorcontrib><creatorcontrib>Villegas-Perez, M.P.</creatorcontrib><creatorcontrib>Charteris, D.G.</creatorcontrib><creatorcontrib>Fitzke, F.W.</creatorcontrib><creatorcontrib>Greenwood, J.</creatorcontrib><creatorcontrib>Lund, R.D.</creatorcontrib><title>High resolution imaging of fluorescein patterns in RCS rat retinae and their direct correlation with histology</title><title>Experimental eye research</title><addtitle>Exp Eye Res</addtitle><description>To assess the progressive changes in the retinal vascular bed of dystrophic and non-dystrophic Royal College of Surgeons (RCS) rats, retinae, were visualised correlating in vivo fundus fluorescein angiography (FA) with histology.
FA was performed in rats aged 5 weeks to 2 years, using a Zeiss confocal scanning laser ophthalmoscope (cSLO). After the final imaging session, a subset of retinae were prepared for flat-mount histology and the vascular bed was visualised using nicotinamide adenine dinucleotide phosphate-diaphorase (NADPH-d) staining. While non-dystrophic rat retinae showed no substantive changes in vascular patterns with age and no demonstrable fluorescein leakage up to at least 1 year, dystrophic rat retinae showed abnormal vascular formations, demonstrable on FA and NADPH-d staining, which could be correlated in single retinae. Hyperfluorescent spots and late angiographic leakage were evident beginning at 10 weeks and progressed in severity with time: they were coincident in distribution with abnormal histological vascular complexes.
The ability to monitor the same retina serially makes this approach a valuable tool for studying the dynamics of vascular change in the diseased retina, not only during the course of degeneration but also when assessing efficacy of potential therapeutic approaches.</description><subject>Animals</subject><subject>confocal scanning ophthalmoscope</subject><subject>Disease Progression</subject><subject>Fluorescein Angiography</subject><subject>Microscopy, Confocal</subject><subject>Muscular Dystrophies - pathology</subject><subject>Rats</subject><subject>Rats, Mutant Strains</subject><subject>RCS rats</subject><subject>retina</subject><subject>Retina - pathology</subject><subject>Retinal Degeneration - pathology</subject><subject>Retinal Ganglion Cells - pathology</subject><subject>Retinal Vessels - pathology</subject><subject>vascular</subject><issn>0014-4835</issn><issn>1096-0007</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEFr3DAQhUVpaTZp_0APQafe7I4sWbahl7K0TSBQaHMXsjza1eKVNpKcNP--2uxCbj3NMPPeg_cR8olBzYDJL7sa_2KsG4C2BlkDyDdkxWCQFQB0b8kKgIlK9Ly9IJcp7cqVi068JxdMQisYlyvib9xmSyOmMC_ZBU_dXm-c39BgqZ2XUD4GnacHnTNGn2jZf6__0KhzcWXnNVLtJ5q36CKdXESTqQkx4qxf8p5c3tKtSznMYfP8gbyzek748TyvyP2P7_frm-ru18_b9be7yvBW5EpPehwaLZvJCgBrYRi7iY8aJsthtGjEOI7AeCuZbAfDhRjsoFnfd63ooOdX5PMp9hDDw4Ipq70rPeZZewxLUh3IviBsirA5CU0MKUW06hALgfisGKgjZLVTR8jqCFmBVAVyMV2f05dxj9Or5Uy1CL6eBFgqPrpiT8ahN3jio6bg_pf_D4gWj7Y</recordid><startdate>2006</startdate><enddate>2006</enddate><creator>Zambarakji, H.J.</creator><creator>Keegan, D.J.</creator><creator>Holmes, T.M.</creator><creator>Halfyard, A.S.</creator><creator>Villegas-Perez, M.P.</creator><creator>Charteris, D.G.</creator><creator>Fitzke, F.W.</creator><creator>Greenwood, J.</creator><creator>Lund, R.D.</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>2006</creationdate><title>High resolution imaging of fluorescein patterns in RCS rat retinae and their direct correlation with histology</title><author>Zambarakji, H.J. ; Keegan, D.J. ; Holmes, T.M. ; Halfyard, A.S. ; Villegas-Perez, M.P. ; Charteris, D.G. ; Fitzke, F.W. ; Greenwood, J. ; Lund, R.D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c354t-adab92a62df400ff09b7d3ba0df30bfec4bbb013561659c3449f9a1887547083</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Animals</topic><topic>confocal scanning ophthalmoscope</topic><topic>Disease Progression</topic><topic>Fluorescein Angiography</topic><topic>Microscopy, Confocal</topic><topic>Muscular Dystrophies - pathology</topic><topic>Rats</topic><topic>Rats, Mutant Strains</topic><topic>RCS rats</topic><topic>retina</topic><topic>Retina - pathology</topic><topic>Retinal Degeneration - pathology</topic><topic>Retinal Ganglion Cells - pathology</topic><topic>Retinal Vessels - pathology</topic><topic>vascular</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zambarakji, H.J.</creatorcontrib><creatorcontrib>Keegan, D.J.</creatorcontrib><creatorcontrib>Holmes, T.M.</creatorcontrib><creatorcontrib>Halfyard, A.S.</creatorcontrib><creatorcontrib>Villegas-Perez, M.P.</creatorcontrib><creatorcontrib>Charteris, D.G.</creatorcontrib><creatorcontrib>Fitzke, F.W.</creatorcontrib><creatorcontrib>Greenwood, J.</creatorcontrib><creatorcontrib>Lund, R.D.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Experimental eye research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zambarakji, H.J.</au><au>Keegan, D.J.</au><au>Holmes, T.M.</au><au>Halfyard, A.S.</au><au>Villegas-Perez, M.P.</au><au>Charteris, D.G.</au><au>Fitzke, F.W.</au><au>Greenwood, J.</au><au>Lund, R.D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>High resolution imaging of fluorescein patterns in RCS rat retinae and their direct correlation with histology</atitle><jtitle>Experimental eye research</jtitle><addtitle>Exp Eye Res</addtitle><date>2006</date><risdate>2006</risdate><volume>82</volume><issue>1</issue><spage>164</spage><epage>171</epage><pages>164-171</pages><issn>0014-4835</issn><eissn>1096-0007</eissn><abstract>To assess the progressive changes in the retinal vascular bed of dystrophic and non-dystrophic Royal College of Surgeons (RCS) rats, retinae, were visualised correlating in vivo fundus fluorescein angiography (FA) with histology.
FA was performed in rats aged 5 weeks to 2 years, using a Zeiss confocal scanning laser ophthalmoscope (cSLO). After the final imaging session, a subset of retinae were prepared for flat-mount histology and the vascular bed was visualised using nicotinamide adenine dinucleotide phosphate-diaphorase (NADPH-d) staining. While non-dystrophic rat retinae showed no substantive changes in vascular patterns with age and no demonstrable fluorescein leakage up to at least 1 year, dystrophic rat retinae showed abnormal vascular formations, demonstrable on FA and NADPH-d staining, which could be correlated in single retinae. Hyperfluorescent spots and late angiographic leakage were evident beginning at 10 weeks and progressed in severity with time: they were coincident in distribution with abnormal histological vascular complexes.
The ability to monitor the same retina serially makes this approach a valuable tool for studying the dynamics of vascular change in the diseased retina, not only during the course of degeneration but also when assessing efficacy of potential therapeutic approaches.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>16054136</pmid><doi>10.1016/j.exer.2005.06.006</doi><tpages>8</tpages></addata></record> |
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subjects | Animals confocal scanning ophthalmoscope Disease Progression Fluorescein Angiography Microscopy, Confocal Muscular Dystrophies - pathology Rats Rats, Mutant Strains RCS rats retina Retina - pathology Retinal Degeneration - pathology Retinal Ganglion Cells - pathology Retinal Vessels - pathology vascular |
title | High resolution imaging of fluorescein patterns in RCS rat retinae and their direct correlation with histology |
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