Early markers of retinal degeneration in rd/rd mice

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dc.contributor.author Acosta Etchebarne, Monica en
dc.contributor.author Fletcher, EL en
dc.contributor.author Azizoglu, Serap en
dc.contributor.author Foster, LE en
dc.contributor.author Farber, DB en
dc.contributor.author Kalloniatis, Michael en
dc.date.accessioned 2017-12-05T20:54:45Z en
dc.date.available 2005-07-29 en
dc.date.issued 2005-09-06 en
dc.identifier.citation Molecular Vision, 11, 717-728, 06 Sep 2005 en
dc.identifier.issn 1090-0535 en
dc.identifier.uri http://hdl.handle.net/2292/36685 en
dc.description.abstract PURPOSE: In the rd/rd mouse, the cell death of rod photoreceptors has been correlated to abnormal levels of the cyclic nucleotide cGMP within photoreceptors. Given that cGMP is required for opening of the cationic channels, there is the possibility that a high cGMP concentration would maintain these channels open, at a high energy cost for the retina. METHODS: We investigated whether cation channels were maintained in an open state in the rd/rd mouse retina by determining the labeling pattern of an organic cationic probe (agmatine, AGB) which selectively enters cells through open cationic channels. The metabolic activity of the rd/rd mice was measured by assaying lactate dehydrogenase (LDH) activity in several tissues and Na+/K+ ATPase activity was measured as a function of development and degeneration of the retina. RESULTS: AGB neuronal labeling showed a systematic increase consistent with the known neuronal functional maturation in the normal retina. There was a significant higher AGB labeling of photoreceptors in the rd/rd mouse retina from P6 supporting the possibility of open cationic channels from an early age. There were no changes in the LDH activity of tissues that contain PDE6 or that have a similar LDH distribution as the retina. However, LDH activity was significantly higher in the rd/rd mouse retina than in those of control mice from birth to P6, and it dramatically decreased from P9 as the photoreceptors degenerated. The predominant LDH isoenzyme changes and loss after degeneration appeared to be LDH5. ATPase activity increased with age, reaching adult levels by P16. Unlike LDH activity, there was no significant difference in Na+/K+ ATPase activity between control and rd/rd mice at any age examined. CONCLUSIONS: We conclude that AGB is a useful marker of photoreceptors destined to degenerate. We discard the possibility of a generalized metabolic effect in the rd/rd mice. However, the elevated LDH activity present before photoreceptor differentiation indicated altered retinal metabolic activity that could not be associated with open cationic channels alone. Therefore, altered metabolic activity as indicated by LDH measurements in the retina appeared to be the earliest sensitive sign of future photoreceptor dysfunction in the rd/rd mice. en
dc.description.uri http://www.ncbi.nlm.nih.gov/pubmed/16163270 en
dc.language English en
dc.publisher Molecular Vision en
dc.relation.ispartofseries Molecular Vision en
dc.rights Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher. Details obtained from https://web.archive.org/web/20050204152339/http://www.molvis.org:80/molvis/instructions.html en
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm en
dc.title Early markers of retinal degeneration in rd/rd mice en
dc.type Journal Article en
pubs.begin-page 717 en
pubs.volume 11 en
dc.rights.holder Copyright: Molecular Vision en
dc.identifier.pmid 16163270 en
pubs.author-url http://www.molvis.org/molvis/v11/a85/ en
pubs.end-page 728 en
pubs.publication-status Published en
dc.rights.accessrights http://purl.org/eprint/accessRights/RestrictedAccess en
pubs.subtype Article en
pubs.elements-id 40292 en
pubs.org-id Medical and Health Sciences en
pubs.org-id Optometry and Vision Science en
dc.identifier.eissn 1090-0535 en
pubs.record-created-at-source-date 2010-09-01 en
pubs.dimensions-id 16163270 en


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