Abstract

Delayed dark adaptation due to impaired rod photoreceptor homeostasis has been reported as the earliest symptom of eye diseases such as age-related macular degeneration, diabetic retinopathy, and retinitis pigmentosa. Objective measurement of dark adaptation can facilitate early diagnosis to enable prompt intervention to prevent vision loss. However, there is a lack of noninvasive methods capable of spatiotemporal monitoring of photoreceptor changes during dark adaptation. Here we demonstrate functional optical coherence tomography (OCT) for in vivo intrinsic signal optoretinography (ORG) of dark adaptation kinetics in the C57BL/6J mouse retina. Functional OCT revealed a shortening of the outer retina, a rearrangement of the cone and rod photoreceptor interdigitation zone, and a reduction in intrinsic signal amplitude at the photoreceptor inner segment ellipsoid (ISe). A strong positive correlation between the outer retinal shortening and ISe intensity reduction was also confirmed. Functional OCT of dark adaptation kinetics promises an objective method for rapid ORG assessment of physiological integrity of retinal photoreceptors.

Highlights

  • Delayed dark adaptation due to impaired rod photoreceptor homeostasis has been reported as the earliest symptom of eye diseases such as age-related macular degeneration, diabetic retinopathy, and retinitis pigmentosa

  • In the light-adapted retina, the interdigitation zone (IZ) and outer segments (OS) tip band of the outer retina was distinguished, which was absent in the dark-adapted retina, and a hypo-reflective band between the IZ and retinal pigment epithelium (RPE) band was only observed in the light-adapted retina

  • We found that retinal response during dark adaptation was reflected by transient structural and physiological changes, mainly in the outer retina

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Summary

Introduction

Delayed dark adaptation due to impaired rod photoreceptor homeostasis has been reported as the earliest symptom of eye diseases such as age-related macular degeneration, diabetic retinopathy, and retinitis pigmentosa. We demonstrate functional optical coherence tomography (OCT) for in vivo intrinsic signal optoretinography (ORG) of dark adaptation kinetics in the C57BL/6J mouse retina. Functional OCT of dark adaptation kinetics promises an objective method for rapid ORG assessment of physiological integrity of retinal photoreceptors. Dynamic monitoring of transient structural and reflectivity changes, which promises a biomarker for rapid assessment of functional integrity of dark adaptation in the retina, remains to be explored. We report intrinsic signal ORG assessment of dark adaptation kinetics in the mouse retina in vivo. This study demonstrates the potential of intrinsic signal ORG assessment of dark adaptation kinetics in the living retina

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