Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/89385
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dc.contributorSchool of Optometryen_US
dc.creatorBanerjee, Sen_US
dc.creatorWang, Qen_US
dc.creatorPang, Ken_US
dc.creatorNg, KHHen_US
dc.creatorYuen, SMen_US
dc.creatorPan, Fen_US
dc.date.accessioned2021-03-18T06:32:03Z-
dc.date.available2021-03-18T06:32:03Z-
dc.identifier.issn0146-0404en_US
dc.identifier.urihttp://hdl.handle.net/10397/89385-
dc.description2019 ARVO Annual Meeting, held in Vancouver, Canada, April 28 - May 2, 2019en_US
dc.language.isoenen_US
dc.publisherAssociation for Research in Vision and Ophthalmologyen_US
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/).en_US
dc.rightsThe following publication Seema Banerjee, Qin wang, ko pang, Ng Kai hong henry, Yuen sin man, Feng Pan; Defocused images affect the multi-neuronal firing patterns in the mouse retina-a multielectrode array study. Invest. Ophthalmol. Vis. Sci. 2019;60(9):5286 [Meeting Abstract] is available at https://iovs.arvojournals.org/article.aspx?articleid=2744636.en_US
dc.titleDefocused images affect the multi-neuronal firing patterns in the mouse retina-a multielectrode array studyen_US
dc.typeConference Paperen_US
dc.identifier.spage1en_US
dc.identifier.volume60en_US
dc.identifier.issue9en_US
dcterms.abstractPurpose : Myopia is a substantial public health problem, affecting 33% of individuals over the age of 12 years in the United States and more than 80% people in Hong Kong. Although it is well established that defocused images alter eye growth and refraction contributing to myopia and that the retina can sense the focus of an image, defocused images’s effects on retinal signaling that accounts either for emmetropization or for refractive errors has remained elusive. It is important to identify the cells and to understand the neuronal circuit that contributes to myopia to provide new insight and means for myopia prevention and modulation.en_US
dcterms.abstractMethods : Ganglion cells of the dark-adapted retina from all quadrants were recording from adult C57BL/C57BL:129 wild-type by using 256 channels Multielectrode Arrays (MEAs). For MEA recording, retina–eyecups (n=20) were isolated. Defocused images generated by white or mono green organic light-emitting display (OLEDXL, Olightek, China; 800 × 600-pixel resolution, 85 Hz refresh rate) was controlled by computer and was presented different spatial frequencies light bar generated by PsychoPy onto the photoreceptor layer. The intensity of the light bar was above 100 isomerizations (R*)/rod/s in the photopic range were applied on the surface of the retina. The data was analyzed by using Offline Sorter (Plexon, Dallas, TX, USA) and NeuroExplorer (Nex Technologies, Littleton, MA, USA) software.en_US
dcterms.abstractResults : Dark-adapted mouse ganglion cells (GCs) were recording under different light intensity to find their thresholds and intensity-response profiles. The firing patterns of GCs varied under the different powers of defocused images. OFF delayed cell (GCs or amacrine cells (ACs) with time latency more than 2 seconds, had synchrony firing with GCs and/or ACs. The spatial synchrony firing pattern between OFF delayed cell and other GCs/ACs had significantly change after image defocused. Compared with focused image, the number of synchronized cells with OFF delayed cell decreased with increased power of defocused images.en_US
dcterms.abstractConclusions : Our results showed that defocused images induced multi-neuronal firing patterns changed in the mouse retina. Spatial firing patterns varied with different powers of defocused images. Synchrony firing of OFF-delayed cells possibly related to edge detection, a potential therapeutic target for myopia patients in future.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationInvestigative ophthalmology and visual science, July 2019, v. 60, no. 9, 5286, p. 1 [Meeting Abstract]en_US
dcterms.isPartOfInvestigative ophthalmology and visual scienceen_US
dcterms.issued2019-07-
dc.relation.conferenceARVO. Annual Meetingen_US
dc.identifier.eissn1552-5783en_US
dc.identifier.artn5286en_US
dc.description.validate202103 bcrcen_US
dc.description.oaOther Versionen_US
dc.identifier.FolderNumbera0644-n03en_US
dc.identifier.SubFormID706-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextP0000341, P0000465, P0008663en_US
dc.description.pubStatusPublisheden_US
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