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Herbal Supplement in a Buffer for Dry Eye Syndrome Treatment

Dry eye syndrome (DES) is one of the most common types of ocular diseases. There is a major need to treat DES in a simple yet efficient way. Artificial tears (AT) are the most commonly used agents for treating DES, but are not very effective. Herbal extractions of ferulic acid (FA), an anti-oxidant...

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Autores principales: Chen, Hung-Chang, Chen, Zhi-Yu, Wang, Tsung-Jen, Drew, Victor J., Tseng, Ching-Li, Fang, Hsu-Wei, Lin, Feng-Huei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5578087/
https://www.ncbi.nlm.nih.gov/pubmed/28771187
http://dx.doi.org/10.3390/ijms18081697
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author Chen, Hung-Chang
Chen, Zhi-Yu
Wang, Tsung-Jen
Drew, Victor J.
Tseng, Ching-Li
Fang, Hsu-Wei
Lin, Feng-Huei
author_facet Chen, Hung-Chang
Chen, Zhi-Yu
Wang, Tsung-Jen
Drew, Victor J.
Tseng, Ching-Li
Fang, Hsu-Wei
Lin, Feng-Huei
author_sort Chen, Hung-Chang
collection PubMed
description Dry eye syndrome (DES) is one of the most common types of ocular diseases. There is a major need to treat DES in a simple yet efficient way. Artificial tears (AT) are the most commonly used agents for treating DES, but are not very effective. Herbal extractions of ferulic acid (FA), an anti-oxidant agent, and kaempferol (KM), an anti-inflammatory reagent, were added to buffer solution (BS) to replace ATs for DES treatment. The cytotoxicity and anti-inflammatory effects were examined in vitro by co-culture with human corneal epithelial cells (HCECs) to obtain the optimal concentration of KM and FA for treating HCECs. Physical properties of BS, such as pH value, osmolality, and refractive index were also examined. Then, rabbits with DES were used for therapeutic evaluation. Tear production, corneal damage, and ocular irritation in rabbits’ eyes were examined. The non-toxic concentrations of KM and FA for HCEC cultivation over 3 days were 1 µM and 100 µM, respectively. Live/dead stain results also show non-toxicity of KM and FA for treating HCECs. Lipopolysaccharide-stimulated HCECs in inflammatory conditions treated with 100 µM FA and 1 µM KM (FA100/KM1) showed lower IL-1B, IL-6, IL-8, and TNFα expression when examined by real-time PCR. The BS with FA100/KM1 had neutral pH, and a similar osmolality and refractive index to human tears. Topical delivery of BS + FA100/KM1 showed no irritation to rabbit eyes. The corneal thickness in the BS + FA100/KM1 treated group was comparable to normal eyes. Results of DES rabbits treated with BS + FA100/KM1 showed less corneal epithelial damage and higher tear volume than the normal group. In conclusion, we showed that the combination of FA (100 µM) and KM (1 µM) towards treating inflamed HCECs had an anti-inflammatory effect, and it is effective in treating DES rabbits when BS is added in combination with these two herbal supplements and used as a topical eye drop.
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spelling pubmed-55780872017-09-05 Herbal Supplement in a Buffer for Dry Eye Syndrome Treatment Chen, Hung-Chang Chen, Zhi-Yu Wang, Tsung-Jen Drew, Victor J. Tseng, Ching-Li Fang, Hsu-Wei Lin, Feng-Huei Int J Mol Sci Article Dry eye syndrome (DES) is one of the most common types of ocular diseases. There is a major need to treat DES in a simple yet efficient way. Artificial tears (AT) are the most commonly used agents for treating DES, but are not very effective. Herbal extractions of ferulic acid (FA), an anti-oxidant agent, and kaempferol (KM), an anti-inflammatory reagent, were added to buffer solution (BS) to replace ATs for DES treatment. The cytotoxicity and anti-inflammatory effects were examined in vitro by co-culture with human corneal epithelial cells (HCECs) to obtain the optimal concentration of KM and FA for treating HCECs. Physical properties of BS, such as pH value, osmolality, and refractive index were also examined. Then, rabbits with DES were used for therapeutic evaluation. Tear production, corneal damage, and ocular irritation in rabbits’ eyes were examined. The non-toxic concentrations of KM and FA for HCEC cultivation over 3 days were 1 µM and 100 µM, respectively. Live/dead stain results also show non-toxicity of KM and FA for treating HCECs. Lipopolysaccharide-stimulated HCECs in inflammatory conditions treated with 100 µM FA and 1 µM KM (FA100/KM1) showed lower IL-1B, IL-6, IL-8, and TNFα expression when examined by real-time PCR. The BS with FA100/KM1 had neutral pH, and a similar osmolality and refractive index to human tears. Topical delivery of BS + FA100/KM1 showed no irritation to rabbit eyes. The corneal thickness in the BS + FA100/KM1 treated group was comparable to normal eyes. Results of DES rabbits treated with BS + FA100/KM1 showed less corneal epithelial damage and higher tear volume than the normal group. In conclusion, we showed that the combination of FA (100 µM) and KM (1 µM) towards treating inflamed HCECs had an anti-inflammatory effect, and it is effective in treating DES rabbits when BS is added in combination with these two herbal supplements and used as a topical eye drop. MDPI 2017-08-03 /pmc/articles/PMC5578087/ /pubmed/28771187 http://dx.doi.org/10.3390/ijms18081697 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Chen, Hung-Chang
Chen, Zhi-Yu
Wang, Tsung-Jen
Drew, Victor J.
Tseng, Ching-Li
Fang, Hsu-Wei
Lin, Feng-Huei
Herbal Supplement in a Buffer for Dry Eye Syndrome Treatment
title Herbal Supplement in a Buffer for Dry Eye Syndrome Treatment
title_full Herbal Supplement in a Buffer for Dry Eye Syndrome Treatment
title_fullStr Herbal Supplement in a Buffer for Dry Eye Syndrome Treatment
title_full_unstemmed Herbal Supplement in a Buffer for Dry Eye Syndrome Treatment
title_short Herbal Supplement in a Buffer for Dry Eye Syndrome Treatment
title_sort herbal supplement in a buffer for dry eye syndrome treatment
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5578087/
https://www.ncbi.nlm.nih.gov/pubmed/28771187
http://dx.doi.org/10.3390/ijms18081697
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