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Rosmarinic Acid Restores Complete Transparency of Sonicated Human Cataract Ex Vivo and Delays Cataract Formation In Vivo

Cataract, the leading cause of vision impairment worldwide, arises from abnormal aggregation of crystallin lens proteins. Presently, surgical removal is the only therapeutic approach. Recent findings have triggered renewed interest in development of non-surgical treatment alternatives. However, emer...

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Autores principales: Chemerovski-Glikman, Marina, Mimouni, Michael, Dagan, Yarden, Haj, Esraa, Vainer, Igor, Allon, Raviv, Blumenthal, Eytan Z., Adler-Abramovich, Lihi, Segal, Daniel, Gazit, Ehud, Zayit-Soudry, Shiri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6008418/
https://www.ncbi.nlm.nih.gov/pubmed/29921877
http://dx.doi.org/10.1038/s41598-018-27516-9
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author Chemerovski-Glikman, Marina
Mimouni, Michael
Dagan, Yarden
Haj, Esraa
Vainer, Igor
Allon, Raviv
Blumenthal, Eytan Z.
Adler-Abramovich, Lihi
Segal, Daniel
Gazit, Ehud
Zayit-Soudry, Shiri
author_facet Chemerovski-Glikman, Marina
Mimouni, Michael
Dagan, Yarden
Haj, Esraa
Vainer, Igor
Allon, Raviv
Blumenthal, Eytan Z.
Adler-Abramovich, Lihi
Segal, Daniel
Gazit, Ehud
Zayit-Soudry, Shiri
author_sort Chemerovski-Glikman, Marina
collection PubMed
description Cataract, the leading cause of vision impairment worldwide, arises from abnormal aggregation of crystallin lens proteins. Presently, surgical removal is the only therapeutic approach. Recent findings have triggered renewed interest in development of non-surgical treatment alternatives. However, emerging treatments are yet to achieve full and consistent lens clearance. Here, the first ex vivo assay to screen for drug candidates that reduce human lenticular protein aggregation was developed. This assay allowed the identification of two leading compounds as facilitating the restoration of nearly-complete transparency of phacoemulsified cataractous preparation ex vivo. Mechanistic studies demonstrated that both compounds reduce cataract microparticle size and modify their amyloid-like features. In vivo studies confirmed that the lead compound, rosmarinic acid, delays cataract formation and reduces the severity of lens opacification in model rats. Thus, the ex vivo assay may provide an initial platform for broad screening of potential novel therapeutic agents towards pharmacological treatment of cataract.
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spelling pubmed-60084182018-06-26 Rosmarinic Acid Restores Complete Transparency of Sonicated Human Cataract Ex Vivo and Delays Cataract Formation In Vivo Chemerovski-Glikman, Marina Mimouni, Michael Dagan, Yarden Haj, Esraa Vainer, Igor Allon, Raviv Blumenthal, Eytan Z. Adler-Abramovich, Lihi Segal, Daniel Gazit, Ehud Zayit-Soudry, Shiri Sci Rep Article Cataract, the leading cause of vision impairment worldwide, arises from abnormal aggregation of crystallin lens proteins. Presently, surgical removal is the only therapeutic approach. Recent findings have triggered renewed interest in development of non-surgical treatment alternatives. However, emerging treatments are yet to achieve full and consistent lens clearance. Here, the first ex vivo assay to screen for drug candidates that reduce human lenticular protein aggregation was developed. This assay allowed the identification of two leading compounds as facilitating the restoration of nearly-complete transparency of phacoemulsified cataractous preparation ex vivo. Mechanistic studies demonstrated that both compounds reduce cataract microparticle size and modify their amyloid-like features. In vivo studies confirmed that the lead compound, rosmarinic acid, delays cataract formation and reduces the severity of lens opacification in model rats. Thus, the ex vivo assay may provide an initial platform for broad screening of potential novel therapeutic agents towards pharmacological treatment of cataract. Nature Publishing Group UK 2018-06-19 /pmc/articles/PMC6008418/ /pubmed/29921877 http://dx.doi.org/10.1038/s41598-018-27516-9 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Chemerovski-Glikman, Marina
Mimouni, Michael
Dagan, Yarden
Haj, Esraa
Vainer, Igor
Allon, Raviv
Blumenthal, Eytan Z.
Adler-Abramovich, Lihi
Segal, Daniel
Gazit, Ehud
Zayit-Soudry, Shiri
Rosmarinic Acid Restores Complete Transparency of Sonicated Human Cataract Ex Vivo and Delays Cataract Formation In Vivo
title Rosmarinic Acid Restores Complete Transparency of Sonicated Human Cataract Ex Vivo and Delays Cataract Formation In Vivo
title_full Rosmarinic Acid Restores Complete Transparency of Sonicated Human Cataract Ex Vivo and Delays Cataract Formation In Vivo
title_fullStr Rosmarinic Acid Restores Complete Transparency of Sonicated Human Cataract Ex Vivo and Delays Cataract Formation In Vivo
title_full_unstemmed Rosmarinic Acid Restores Complete Transparency of Sonicated Human Cataract Ex Vivo and Delays Cataract Formation In Vivo
title_short Rosmarinic Acid Restores Complete Transparency of Sonicated Human Cataract Ex Vivo and Delays Cataract Formation In Vivo
title_sort rosmarinic acid restores complete transparency of sonicated human cataract ex vivo and delays cataract formation in vivo
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6008418/
https://www.ncbi.nlm.nih.gov/pubmed/29921877
http://dx.doi.org/10.1038/s41598-018-27516-9
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