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      Optical properties of the mouse eye

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          Abstract

          The Shack-Hartmann wavefront sensor (SHWS) spots upon which ocular aberration measurements depend have poor quality in mice due to light reflected from multiple retinal layers. We have designed and implemented a SHWS that can favor light from a specific retinal layer and measured monochromatic aberrations in 20 eyes from 10 anesthetized C57BL/6J mice. Using this instrument, we show that mice are myopic, not hyperopic as is frequently reported. We have also measured longitudinal chromatic aberration (LCA) of the mouse eye and found that it follows predictions of the water-filled schematic mouse eye. Results indicate that the optical quality of the mouse eye assessed by measurement of its aberrations is remarkably good, better for retinal imaging than the human eye. The dilated mouse eye has a much larger numerical aperture (NA) than that of the dilated human eye (0.5 NA vs. 0.2 NA), but it has a similar amount of root mean square (RMS) higher order aberrations compared to the dilated human eye. These measurements predict that adaptive optics based on this method of wavefront sensing will provide improvements in retinal image quality and potentially two times higher lateral resolution than that in the human eye.

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          The retinex theory of color vision.

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            Optical and retinal factors affecting visual resolution.

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              Physiological Features of the S- and M-cone Photoreceptors of Wild-type Mice from Single-cell Recordings

              Cone cells constitute only 3% of the photoreceptors of the wild-type (WT) mouse. While mouse rods have been thoroughly investigated with suction pipette recordings of their outer segment membrane currents, to date no recordings from WT cones have been published, likely because of the rarity of cones and the fragility of their outer segments. Recently, we characterized the photoreceptors of Nrl −/− mice, using suction pipette recordings from their “inner segments” (perinuclear region), and found them to be cones. Here we report the use of this same method to record for the first time the responses of single cones of WT mice, and of mice lacking the α-subunit of the G-protein transducin (G tα−/−), a loss that renders them functionally rodless. Most cones were found to functionally co-express both S- (λmax = 360 nm) and M- (λmax = 508 nm) cone opsins and to be maximally sensitive at 360 nm (“S-cones”); nonetheless, all cones from the dorsal retina were found to be maximally sensitive at 508 nm (“M-cones”). The dim-flash response kinetics and absolute sensitivity of S- and M-cones were very similar and not dependent on which of the coexpressed cone opsins drove transduction; the time to peak of the dim-flash response was ∼70 ms, and ∼0.2% of the circulating current was suppressed per photoisomerization. Amplification in WT cones (A ∼4 s−2) was found to be about twofold lower than in rods (A ∼8 s−2). Mouse M-cones maintained their circulating current at very nearly the dark adapted level even when >90% of their M-opsin was bleached. S-cones were less tolerant to bleached S-opsin than M-cones to bleached M-opsin, but still far more tolerant than mouse rods to bleached rhodopsin, which exhibit persistent suppression of nearly 50% of their circulating current following a 20% bleach. Thus, the three types of mouse opsin appear distinctive in the degree to which their bleached, unregenerated opsins generate “dark light.”
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                Author and article information

                Journal
                Biomed Opt Express
                BOE
                Biomedical Optics Express
                Optical Society of America
                2156-7085
                01 April 2011
                28 February 2011
                28 February 2011
                : 2
                : 4
                : 717-738
                Affiliations
                [1 ]Center for Visual Science, University of Rochester, Rochester, NY, 14627, USA
                [2 ]The Institute of Optics, University of Rochester, Rochester, NY, 14620, USA
                [3 ]Flaum Eye Institute, University of Rochester, Rochester, NY, 14642, USA
                Author notes
                Article
                139905
                10.1364/BOE.2.000717
                3072116
                21483598
                9176f018-5d60-4eee-b957-88fcc6082403
                ©2011 Optical Society of America

                This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 Unported License, which permits download and redistribution, provided that the original work is properly cited. This license restricts the article from being modified or used commercially.

                History
                : 21 December 2010
                : 23 February 2011
                : 24 February 2011
                Funding
                Funded by: NIH
                Award ID: EY 001319
                Award ID: EY014375
                Award ID: EY018606
                Funded by: NSF
                Award ID: AST-9876783
                Funded by: Research to Prevent Blindness
                Categories
                Vision, Color, and Visual Optics
                Custom metadata
                True
                0

                Vision sciences
                (330.5370) vision, color, and visual optics: physiological optics,(170.4460) medical optics and biotechnology: ophthalmic optics and devices,(110.1080) active or adaptive optics,(330.7324) vision, color, and visual optics: visual optics, comparative animal models,(330.4300) vision system - noninvasive assessment

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