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Anti-glaucoma potential of hesperidin in experimental glaucoma induced rats

Glaucoma is well-known clinical eye conditions that damage the optic nerve due to abnormal pressure conditions in eye. Hesperidin is well-known glycoside widely present in the citrus fruits, and its aglycone form is known as hesperetin. Hesperidin is major flavone found in orange fruits. Hypotensive...

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Autores principales: Lu, Baiyang, Wang, Xue, Ren, Zengjin, Jiang, Haitao, Liu, Bingqian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7235152/
https://www.ncbi.nlm.nih.gov/pubmed/32424444
http://dx.doi.org/10.1186/s13568-020-01027-1
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author Lu, Baiyang
Wang, Xue
Ren, Zengjin
Jiang, Haitao
Liu, Bingqian
author_facet Lu, Baiyang
Wang, Xue
Ren, Zengjin
Jiang, Haitao
Liu, Bingqian
author_sort Lu, Baiyang
collection PubMed
description Glaucoma is well-known clinical eye conditions that damage the optic nerve due to abnormal pressure conditions in eye. Hesperidin is well-known glycoside widely present in the citrus fruits, and its aglycone form is known as hesperetin. Hesperidin is major flavone found in orange fruits. Hypotensive effect of hesperidin in acute and chronic glaucoma rats, glutamate level in vitreous humour and glutathione (GSH) level in aqueous humour were determined following 25, 50 and 100 mg/kg of hesperidin treatment. Acetazolamide (5 mg/kg) was used as positive control. Hesperidin treatment significantly reduced the increased intraocular pressure (IOP) level in dextrose induced ocular hypertension than saline treated rats. The effect of hesperidin was comparable to the positive control acetazolamide. Similarly, hesperidin treatment significantly reduced the IOP level in prednisolone acetate induced ocular hypertension than saline treated rats. In the aqueous humour, hesperidin treatment increased the glutathione level 125%, 184.4% and 231.2% at 25, 50 and 100 mg/kg of hesperidin respectively. In the vitreous humour, hesperidin treatment reduced the glutamate level 9.9%, 13.2% and 25.3% at 25, 50 and 100 mg/kg of hesperidin respectively. Histopathological analysis of normal saline treated rats showed morphological alteration in ciliary bodies. However, rats treated with hesperidin showed the reduced level of morphological alteration in ciliary bodies. Taking all these data together, it is suggested that the hesperidin supplementation was effective against glaucoma in experimental rats.
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spelling pubmed-72351522020-05-27 Anti-glaucoma potential of hesperidin in experimental glaucoma induced rats Lu, Baiyang Wang, Xue Ren, Zengjin Jiang, Haitao Liu, Bingqian AMB Express Original Article Glaucoma is well-known clinical eye conditions that damage the optic nerve due to abnormal pressure conditions in eye. Hesperidin is well-known glycoside widely present in the citrus fruits, and its aglycone form is known as hesperetin. Hesperidin is major flavone found in orange fruits. Hypotensive effect of hesperidin in acute and chronic glaucoma rats, glutamate level in vitreous humour and glutathione (GSH) level in aqueous humour were determined following 25, 50 and 100 mg/kg of hesperidin treatment. Acetazolamide (5 mg/kg) was used as positive control. Hesperidin treatment significantly reduced the increased intraocular pressure (IOP) level in dextrose induced ocular hypertension than saline treated rats. The effect of hesperidin was comparable to the positive control acetazolamide. Similarly, hesperidin treatment significantly reduced the IOP level in prednisolone acetate induced ocular hypertension than saline treated rats. In the aqueous humour, hesperidin treatment increased the glutathione level 125%, 184.4% and 231.2% at 25, 50 and 100 mg/kg of hesperidin respectively. In the vitreous humour, hesperidin treatment reduced the glutamate level 9.9%, 13.2% and 25.3% at 25, 50 and 100 mg/kg of hesperidin respectively. Histopathological analysis of normal saline treated rats showed morphological alteration in ciliary bodies. However, rats treated with hesperidin showed the reduced level of morphological alteration in ciliary bodies. Taking all these data together, it is suggested that the hesperidin supplementation was effective against glaucoma in experimental rats. Springer Berlin Heidelberg 2020-05-18 /pmc/articles/PMC7235152/ /pubmed/32424444 http://dx.doi.org/10.1186/s13568-020-01027-1 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Original Article
Lu, Baiyang
Wang, Xue
Ren, Zengjin
Jiang, Haitao
Liu, Bingqian
Anti-glaucoma potential of hesperidin in experimental glaucoma induced rats
title Anti-glaucoma potential of hesperidin in experimental glaucoma induced rats
title_full Anti-glaucoma potential of hesperidin in experimental glaucoma induced rats
title_fullStr Anti-glaucoma potential of hesperidin in experimental glaucoma induced rats
title_full_unstemmed Anti-glaucoma potential of hesperidin in experimental glaucoma induced rats
title_short Anti-glaucoma potential of hesperidin in experimental glaucoma induced rats
title_sort anti-glaucoma potential of hesperidin in experimental glaucoma induced rats
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7235152/
https://www.ncbi.nlm.nih.gov/pubmed/32424444
http://dx.doi.org/10.1186/s13568-020-01027-1
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