[HTML][HTML] Quantitative mapping of ion channel regulation by visual cycle activity in rodent photoreceptors in vivo

BA Berkowitz, R Roberts, DA Oleske… - … & visual science, 2009 - arvojournals.org
BA Berkowitz, R Roberts, DA Oleske, M Chang, S Schafer, D Bissig, M Gradianu
Investigative ophthalmology & visual science, 2009arvojournals.org
purpose. To test the hypothesis that the extent of outer retina uptake of manganese,
measured noninvasively with manganese-enhanced MRI (MEMRI), is a quantitative
biomarker of photoreceptor ion channel regulation by visual cycle activity. methods. Four
groups of animals were studied: control rats adapted to three different background light
intensities, dark-adapted control mice systemically pretreated with retinylamine, and dark-
adapted mice with a nonsense mutation in exon 3 of the RPE65 gene (RPE65 rd12) with …
Abstract
purpose. To test the hypothesis that the extent of outer retina uptake of manganese, measured noninvasively with manganese-enhanced MRI (MEMRI), is a quantitative biomarker of photoreceptor ion channel regulation by visual cycle activity.
methods. Four groups of animals were studied: control rats adapted to three different background light intensities, dark-adapted control mice systemically pretreated with retinylamine, and dark-adapted mice with a nonsense mutation in exon 3 of the RPE65 gene (RPE65 rd12) with and without systemic 11-cis-retinal pretreatment. In all cases, rodents were anesthetized and studied with MEMRI 4 hours after manganese administration IP. Central retinal thickness and intraretinal ion channel regulation were measured from the MEMRI data.
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