Development and degeneration of retina in rds mutant mice: The electroretinogram

In mice, homozygous for the retinal degeneration slow ( rds) gene, the photoreceptor cells lack outer segment disc structures, contain low amounts of rhodopsin, and degenerate slowly, while the inner retinal layers remain intact. The electroretinogram (ERG) from 1-month-old mutant mice shows a lower...

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Veröffentlicht in:Neuroscience letters 1984-07, Vol.48 (2), p.231-237
Hauptverfasser: Reuter, J.H., Sanyal, S.
Format: Artikel
Sprache:eng
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Zusammenfassung:In mice, homozygous for the retinal degeneration slow ( rds) gene, the photoreceptor cells lack outer segment disc structures, contain low amounts of rhodopsin, and degenerate slowly, while the inner retinal layers remain intact. The electroretinogram (ERG) from 1-month-old mutant mice shows a lower than normal amplitude but the time-to-peak is normal. The ERGs from mutant mice of 2–3 months and 6–7 months of age show a further decline in response amplitude as the receptor cell population is depleted with progress of degeneration while the time-to-peak increases. The ERG is absent in 1-year-old mutant mice which have lost their receptor cells completely. The possible morphological correlations of the ERG and its components in the rds mutant mice are discussed.
ISSN:0304-3940
1872-7972
DOI:10.1016/0304-3940(84)90024-7