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Retinal phototoxicity in a novel murine model of intraocular lens implantation

PURPOSE: To establish a novel murine intraocular lens (IOL) implantation model to study the protective effects of colored-IOLs against retinal phototoxicity. METHODS: Two-millimeter diameter IOL buttons were created from IOLs for clinical use. Extra-capsular crystalline lens extraction and IOL impla...

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Autores principales: Kurihara, Toshihide, Omoto, Masahiro, Noda, Kousuke, Ebinuma, Mari, Kubota, Shunsuke, Koizumi, Haruna, Yoshida, Satoru, Ozawa, Yoko, Shimmura, Shigeto, Ishida, Susumu, Tsubota, Kazuo
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2793903/
https://www.ncbi.nlm.nih.gov/pubmed/20019883
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author Kurihara, Toshihide
Omoto, Masahiro
Noda, Kousuke
Ebinuma, Mari
Kubota, Shunsuke
Koizumi, Haruna
Yoshida, Satoru
Ozawa, Yoko
Shimmura, Shigeto
Ishida, Susumu
Tsubota, Kazuo
author_facet Kurihara, Toshihide
Omoto, Masahiro
Noda, Kousuke
Ebinuma, Mari
Kubota, Shunsuke
Koizumi, Haruna
Yoshida, Satoru
Ozawa, Yoko
Shimmura, Shigeto
Ishida, Susumu
Tsubota, Kazuo
author_sort Kurihara, Toshihide
collection PubMed
description PURPOSE: To establish a novel murine intraocular lens (IOL) implantation model to study the protective effects of colored-IOLs against retinal phototoxicity. METHODS: Two-millimeter diameter IOL buttons were created from IOLs for clinical use. Extra-capsular crystalline lens extraction and IOL implantation were performed in BALB/c mice using a technique similar to human cataract surgery. For light exposure experiments, mice were exposed to 5,000 LUX of white light for 24 h on the day after surgery. To investigate the protective effects of yellow IOL against light exposure, ERG measurements were conducted in vivo, followed by TdT-mediated dUTP Nick-End Labeling (TUNEL) and outer nuclear layer (ONL) thickness measurement of retinal tissue in yellow or clear IOL-implanted mice and control mice without surgery. RESULTS: IOLs were successfully implanted in all animals, and IOL buttons without haptics were well stabilized in the capsular bag. Murine eyes developed posterior capsule opacification (PCO) after IOL implantation by postoperative day 5 at the latest. In contrast to the clear IOL-implanted animals stimulated by light exposure, the yellow IOL-implanted animals had significantly reduced numbers of TUNEL-positive cells and retained thickness of the ONL. The ERG showed that yellow IOL implantation prevents a decrease of amplitude in both the a-wave and b-wave compared with clear IOL implantation. CONCLUSIONS: We established a new animal model of IOL implantation and demonstrated the protective effects of colored-IOL against retinal phototoxicity after cataract surgery.
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spelling pubmed-27939032009-12-17 Retinal phototoxicity in a novel murine model of intraocular lens implantation Kurihara, Toshihide Omoto, Masahiro Noda, Kousuke Ebinuma, Mari Kubota, Shunsuke Koizumi, Haruna Yoshida, Satoru Ozawa, Yoko Shimmura, Shigeto Ishida, Susumu Tsubota, Kazuo Mol Vis Research Article PURPOSE: To establish a novel murine intraocular lens (IOL) implantation model to study the protective effects of colored-IOLs against retinal phototoxicity. METHODS: Two-millimeter diameter IOL buttons were created from IOLs for clinical use. Extra-capsular crystalline lens extraction and IOL implantation were performed in BALB/c mice using a technique similar to human cataract surgery. For light exposure experiments, mice were exposed to 5,000 LUX of white light for 24 h on the day after surgery. To investigate the protective effects of yellow IOL against light exposure, ERG measurements were conducted in vivo, followed by TdT-mediated dUTP Nick-End Labeling (TUNEL) and outer nuclear layer (ONL) thickness measurement of retinal tissue in yellow or clear IOL-implanted mice and control mice without surgery. RESULTS: IOLs were successfully implanted in all animals, and IOL buttons without haptics were well stabilized in the capsular bag. Murine eyes developed posterior capsule opacification (PCO) after IOL implantation by postoperative day 5 at the latest. In contrast to the clear IOL-implanted animals stimulated by light exposure, the yellow IOL-implanted animals had significantly reduced numbers of TUNEL-positive cells and retained thickness of the ONL. The ERG showed that yellow IOL implantation prevents a decrease of amplitude in both the a-wave and b-wave compared with clear IOL implantation. CONCLUSIONS: We established a new animal model of IOL implantation and demonstrated the protective effects of colored-IOL against retinal phototoxicity after cataract surgery. Molecular Vision 2009-12-12 /pmc/articles/PMC2793903/ /pubmed/20019883 Text en Copyright © 2008 Molecular Vision. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Kurihara, Toshihide
Omoto, Masahiro
Noda, Kousuke
Ebinuma, Mari
Kubota, Shunsuke
Koizumi, Haruna
Yoshida, Satoru
Ozawa, Yoko
Shimmura, Shigeto
Ishida, Susumu
Tsubota, Kazuo
Retinal phototoxicity in a novel murine model of intraocular lens implantation
title Retinal phototoxicity in a novel murine model of intraocular lens implantation
title_full Retinal phototoxicity in a novel murine model of intraocular lens implantation
title_fullStr Retinal phototoxicity in a novel murine model of intraocular lens implantation
title_full_unstemmed Retinal phototoxicity in a novel murine model of intraocular lens implantation
title_short Retinal phototoxicity in a novel murine model of intraocular lens implantation
title_sort retinal phototoxicity in a novel murine model of intraocular lens implantation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2793903/
https://www.ncbi.nlm.nih.gov/pubmed/20019883
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