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Antioxidant and Hepatoprotective Activity of a New Tablets Formulation from Tamarindus indica L.
Hepatotoxic chemicals damage liver cells primarily by producing reactive oxygen species. The decoction of the leaves of Tamarindus indica L. is used for liver disorders. In this work we evaluated the hepatoprotective activity of a tablet formulation of this plant. Thirty-five Sprague Dawley rats wer...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4838804/ https://www.ncbi.nlm.nih.gov/pubmed/27143986 http://dx.doi.org/10.1155/2016/3918219 |
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author | Rodriguez Amado, Jesús Rafael Lafourcade Prada, Ariadna Escalona Arranz, Julio Cesar Pérez Rosés, Renato Morris Quevedo, Humberto Keita, Hady Puente Zapata, Edgar Pinho Fernandes, Caio Tavares Carvalho, José Carlos |
author_facet | Rodriguez Amado, Jesús Rafael Lafourcade Prada, Ariadna Escalona Arranz, Julio Cesar Pérez Rosés, Renato Morris Quevedo, Humberto Keita, Hady Puente Zapata, Edgar Pinho Fernandes, Caio Tavares Carvalho, José Carlos |
author_sort | Rodriguez Amado, Jesús Rafael |
collection | PubMed |
description | Hepatotoxic chemicals damage liver cells primarily by producing reactive oxygen species. The decoction of the leaves of Tamarindus indica L. is used for liver disorders. In this work we evaluated the hepatoprotective activity of a tablet formulation of this plant. Thirty-five Sprague Dawley rats were randomly divided into five groups (n = 7). First group (I) is control group, fed with standard diet. Groups II to V (hepatotoxic groups) were subjected to a subcutaneous injection of CCl(4) (0.5 mL/kg). Group II was negative control, fed with standard diet; group III was subjected to administration of Silymarin 150 mg/kg and groups IV and V were treated with tablets in dose of 100 mg/kg and 200 mg/kg, respectively. Lipid peroxidation and the activity of superoxide dismutase, catalase, and reduced glutathione were evaluated. Serum levels of alanine aminotransferase, aspartate aminotransferase, gamma-glutamine transferase, alkaline phosphatase, and a lipid profile were evaluated too. The tablets inhibit lipid peroxidation. The redox balance (SOD-CAT-GSH) remains normal in the experimental groups treated with tablets. The liver function using dose of 200 mg/kg of tablets was better than the other experimental groups. These results justify, scientifically, the ethnobotanical use of the leaves of Tamarindus indica L. |
format | Online Article Text |
id | pubmed-4838804 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-48388042016-05-03 Antioxidant and Hepatoprotective Activity of a New Tablets Formulation from Tamarindus indica L. Rodriguez Amado, Jesús Rafael Lafourcade Prada, Ariadna Escalona Arranz, Julio Cesar Pérez Rosés, Renato Morris Quevedo, Humberto Keita, Hady Puente Zapata, Edgar Pinho Fernandes, Caio Tavares Carvalho, José Carlos Evid Based Complement Alternat Med Research Article Hepatotoxic chemicals damage liver cells primarily by producing reactive oxygen species. The decoction of the leaves of Tamarindus indica L. is used for liver disorders. In this work we evaluated the hepatoprotective activity of a tablet formulation of this plant. Thirty-five Sprague Dawley rats were randomly divided into five groups (n = 7). First group (I) is control group, fed with standard diet. Groups II to V (hepatotoxic groups) were subjected to a subcutaneous injection of CCl(4) (0.5 mL/kg). Group II was negative control, fed with standard diet; group III was subjected to administration of Silymarin 150 mg/kg and groups IV and V were treated with tablets in dose of 100 mg/kg and 200 mg/kg, respectively. Lipid peroxidation and the activity of superoxide dismutase, catalase, and reduced glutathione were evaluated. Serum levels of alanine aminotransferase, aspartate aminotransferase, gamma-glutamine transferase, alkaline phosphatase, and a lipid profile were evaluated too. The tablets inhibit lipid peroxidation. The redox balance (SOD-CAT-GSH) remains normal in the experimental groups treated with tablets. The liver function using dose of 200 mg/kg of tablets was better than the other experimental groups. These results justify, scientifically, the ethnobotanical use of the leaves of Tamarindus indica L. Hindawi Publishing Corporation 2016 2016-04-07 /pmc/articles/PMC4838804/ /pubmed/27143986 http://dx.doi.org/10.1155/2016/3918219 Text en Copyright © 2016 Jesús Rafael Rodriguez Amado et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under 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 Rodriguez Amado, Jesús Rafael Lafourcade Prada, Ariadna Escalona Arranz, Julio Cesar Pérez Rosés, Renato Morris Quevedo, Humberto Keita, Hady Puente Zapata, Edgar Pinho Fernandes, Caio Tavares Carvalho, José Carlos Antioxidant and Hepatoprotective Activity of a New Tablets Formulation from Tamarindus indica L. |
title | Antioxidant and Hepatoprotective Activity of a New Tablets Formulation from Tamarindus indica L. |
title_full | Antioxidant and Hepatoprotective Activity of a New Tablets Formulation from Tamarindus indica L. |
title_fullStr | Antioxidant and Hepatoprotective Activity of a New Tablets Formulation from Tamarindus indica L. |
title_full_unstemmed | Antioxidant and Hepatoprotective Activity of a New Tablets Formulation from Tamarindus indica L. |
title_short | Antioxidant and Hepatoprotective Activity of a New Tablets Formulation from Tamarindus indica L. |
title_sort | antioxidant and hepatoprotective activity of a new tablets formulation from tamarindus indica l. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4838804/ https://www.ncbi.nlm.nih.gov/pubmed/27143986 http://dx.doi.org/10.1155/2016/3918219 |
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