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Evaluation of anticataract potential of Triphala in selenite-induced cataract: In vitro and in vivo studies

Triphala (TP) is composed of Emblica officinalis, Terminalia chebula, and Terminalia belerica. The present study was undertaken to evaluate its anticataract potential in vitro and in vivo in a selenite-induced experimental model of cataract. In vitro enucleated rat lenses were maintained in organ cu...

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Autores principales: Gupta, Suresh Kumar, Kalaiselvan, V., Srivastava, Sushma, Agrawal, Shyam S., Saxena, Rohit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3117320/
https://www.ncbi.nlm.nih.gov/pubmed/21731375
http://dx.doi.org/10.4103/0975-9476.74425
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author Gupta, Suresh Kumar
Kalaiselvan, V.
Srivastava, Sushma
Agrawal, Shyam S.
Saxena, Rohit
author_facet Gupta, Suresh Kumar
Kalaiselvan, V.
Srivastava, Sushma
Agrawal, Shyam S.
Saxena, Rohit
author_sort Gupta, Suresh Kumar
collection PubMed
description Triphala (TP) is composed of Emblica officinalis, Terminalia chebula, and Terminalia belerica. The present study was undertaken to evaluate its anticataract potential in vitro and in vivo in a selenite-induced experimental model of cataract. In vitro enucleated rat lenses were maintained in organ culture containing Dulbecco’s Modified Eagles Medium alone or with the addition of 100μM selenite. These served as the normal and control groups, respectively. In the test group, the medium was supplemented with selenite and different concentrations of TP aqueous extract. The lenses were incubated for 24 h at 37°C. After incubation, the lenses were processed to estimate reduced glutathione (GSH), lipid peroxidation product, and antioxidant enzymes. In vivo selenite cataract was induced in 9-day-old rat pups by subcutaneous injection of sodium selenite (25 μmole/kg body weight). The test groups received 25, 50, and 75 mg/kg of TP intraperitoneally 4 h before the selenite challenge. At the end of the study period, the rats’ eyes were examined by slit-lamp. TP significantly (P < 0.01) restored GSH and decreased malondialdehyde levels. A significant restoration in the activities of antioxidant enzymes such as superoxide dismutase (P < 0.05), catalase (P < 0.05), glutathione peroxidase (P < 0.05), and glutathione-s-transferase (P < 0.005) was observed in the TP-supplemented group compared to controls. In vivo TF 25mg/kg developed only 20% nuclear cataract as compared to 100% in control. TP prevents or retards experimental selenite-induced cataract. This effect may be due to antioxidant activity. Further studies are warranted to explore its role in human cataract.
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spelling pubmed-31173202011-06-30 Evaluation of anticataract potential of Triphala in selenite-induced cataract: In vitro and in vivo studies Gupta, Suresh Kumar Kalaiselvan, V. Srivastava, Sushma Agrawal, Shyam S. Saxena, Rohit J Ayurveda Integr Med Experimental Triphala (TP) is composed of Emblica officinalis, Terminalia chebula, and Terminalia belerica. The present study was undertaken to evaluate its anticataract potential in vitro and in vivo in a selenite-induced experimental model of cataract. In vitro enucleated rat lenses were maintained in organ culture containing Dulbecco’s Modified Eagles Medium alone or with the addition of 100μM selenite. These served as the normal and control groups, respectively. In the test group, the medium was supplemented with selenite and different concentrations of TP aqueous extract. The lenses were incubated for 24 h at 37°C. After incubation, the lenses were processed to estimate reduced glutathione (GSH), lipid peroxidation product, and antioxidant enzymes. In vivo selenite cataract was induced in 9-day-old rat pups by subcutaneous injection of sodium selenite (25 μmole/kg body weight). The test groups received 25, 50, and 75 mg/kg of TP intraperitoneally 4 h before the selenite challenge. At the end of the study period, the rats’ eyes were examined by slit-lamp. TP significantly (P < 0.01) restored GSH and decreased malondialdehyde levels. A significant restoration in the activities of antioxidant enzymes such as superoxide dismutase (P < 0.05), catalase (P < 0.05), glutathione peroxidase (P < 0.05), and glutathione-s-transferase (P < 0.005) was observed in the TP-supplemented group compared to controls. In vivo TF 25mg/kg developed only 20% nuclear cataract as compared to 100% in control. TP prevents or retards experimental selenite-induced cataract. This effect may be due to antioxidant activity. Further studies are warranted to explore its role in human cataract. Medknow Publications 2010 /pmc/articles/PMC3117320/ /pubmed/21731375 http://dx.doi.org/10.4103/0975-9476.74425 Text en © Journal of Ayurveda and Integrative Medicine http://creativecommons.org/licenses/by/2.0/ 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 Experimental
Gupta, Suresh Kumar
Kalaiselvan, V.
Srivastava, Sushma
Agrawal, Shyam S.
Saxena, Rohit
Evaluation of anticataract potential of Triphala in selenite-induced cataract: In vitro and in vivo studies
title Evaluation of anticataract potential of Triphala in selenite-induced cataract: In vitro and in vivo studies
title_full Evaluation of anticataract potential of Triphala in selenite-induced cataract: In vitro and in vivo studies
title_fullStr Evaluation of anticataract potential of Triphala in selenite-induced cataract: In vitro and in vivo studies
title_full_unstemmed Evaluation of anticataract potential of Triphala in selenite-induced cataract: In vitro and in vivo studies
title_short Evaluation of anticataract potential of Triphala in selenite-induced cataract: In vitro and in vivo studies
title_sort evaluation of anticataract potential of triphala in selenite-induced cataract: in vitro and in vivo studies
topic Experimental
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3117320/
https://www.ncbi.nlm.nih.gov/pubmed/21731375
http://dx.doi.org/10.4103/0975-9476.74425
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