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The Effects of Aloe Vera on TNF-a Levels, the Percentage of Nk Cells and Th 17 Cells in Rat That Received Izoniazid and Rifampycin

BACKGROUND: The present study was undertaken to investigate the hepatoprotective effect of Aloe vera against side effect of antituberculosis drug. MATERIAL AND METHODS: Twenty-five rats will be divided into five groups, namely the control group (without any treatment), the group of rats treated with...

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Autores principales: Mawarti, Herin, Rajin, Mukhamad, Asumta, Zulfikar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AVICENA, d.o.o., Sarajevo 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5723184/
https://www.ncbi.nlm.nih.gov/pubmed/29284895
http://dx.doi.org/10.5455/medarh.2017.71.308-311
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author Mawarti, Herin
Rajin, Mukhamad
Asumta, Zulfikar
author_facet Mawarti, Herin
Rajin, Mukhamad
Asumta, Zulfikar
author_sort Mawarti, Herin
collection PubMed
description BACKGROUND: The present study was undertaken to investigate the hepatoprotective effect of Aloe vera against side effect of antituberculosis drug. MATERIAL AND METHODS: Twenty-five rats will be divided into five groups, namely the control group (without any treatment), the group of rats treated with anti-tuberculosis drugs, and a group of rats were treated antituberculosis drugs and got Aloe vera extract at a dose of 40; 80; and 120 mg/kg body weight. Antituberculosis drugs are isoniazid and rifampicin a dose of 50 mg/kg body weight. RESULTS: Antituberculosis treated group showed significantly increase levels of TNF-a, the percentage of NK cells and the number of Th17 cells compared with the control group (p < 0.05). All doses of Aloe vera reduce levels of TNF-a compared with the antituberculosis group (p < 0.05), although it has not yet reached levels comparable to the control group (p > 0.05). Aloe vera at first and the third dose lower the number of NK cells compared to the antituberculosis group, although it has not yet reached a significant difference (p > 0.05). The first dose of Aloe vera was significantly decreased the percentage of Th17 cells compared to the antituberculosis drug group (p < 0.05), although it has not yet reached levels comparable to the control group (p > 0.05). CONCLUSIONS: It was concluded that administration of Aloe vera can suppress the production of TNF-a and the percentage of Th17 cells as a result of antituberculosis drug administration. Thus, Aloe vera can be a useful alternative to natural materials in the successful treatment of tuberculosis through the inhibition of side effect.
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spelling pubmed-57231842017-12-28 The Effects of Aloe Vera on TNF-a Levels, the Percentage of Nk Cells and Th 17 Cells in Rat That Received Izoniazid and Rifampycin Mawarti, Herin Rajin, Mukhamad Asumta, Zulfikar Med Arch Original Paper BACKGROUND: The present study was undertaken to investigate the hepatoprotective effect of Aloe vera against side effect of antituberculosis drug. MATERIAL AND METHODS: Twenty-five rats will be divided into five groups, namely the control group (without any treatment), the group of rats treated with anti-tuberculosis drugs, and a group of rats were treated antituberculosis drugs and got Aloe vera extract at a dose of 40; 80; and 120 mg/kg body weight. Antituberculosis drugs are isoniazid and rifampicin a dose of 50 mg/kg body weight. RESULTS: Antituberculosis treated group showed significantly increase levels of TNF-a, the percentage of NK cells and the number of Th17 cells compared with the control group (p < 0.05). All doses of Aloe vera reduce levels of TNF-a compared with the antituberculosis group (p < 0.05), although it has not yet reached levels comparable to the control group (p > 0.05). Aloe vera at first and the third dose lower the number of NK cells compared to the antituberculosis group, although it has not yet reached a significant difference (p > 0.05). The first dose of Aloe vera was significantly decreased the percentage of Th17 cells compared to the antituberculosis drug group (p < 0.05), although it has not yet reached levels comparable to the control group (p > 0.05). CONCLUSIONS: It was concluded that administration of Aloe vera can suppress the production of TNF-a and the percentage of Th17 cells as a result of antituberculosis drug administration. Thus, Aloe vera can be a useful alternative to natural materials in the successful treatment of tuberculosis through the inhibition of side effect. AVICENA, d.o.o., Sarajevo 2017-10 /pmc/articles/PMC5723184/ /pubmed/29284895 http://dx.doi.org/10.5455/medarh.2017.71.308-311 Text en Copyright: © 2017 Herin Mawarti, Mukhamad Rajin, Zulfikar Asumta http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Paper
Mawarti, Herin
Rajin, Mukhamad
Asumta, Zulfikar
The Effects of Aloe Vera on TNF-a Levels, the Percentage of Nk Cells and Th 17 Cells in Rat That Received Izoniazid and Rifampycin
title The Effects of Aloe Vera on TNF-a Levels, the Percentage of Nk Cells and Th 17 Cells in Rat That Received Izoniazid and Rifampycin
title_full The Effects of Aloe Vera on TNF-a Levels, the Percentage of Nk Cells and Th 17 Cells in Rat That Received Izoniazid and Rifampycin
title_fullStr The Effects of Aloe Vera on TNF-a Levels, the Percentage of Nk Cells and Th 17 Cells in Rat That Received Izoniazid and Rifampycin
title_full_unstemmed The Effects of Aloe Vera on TNF-a Levels, the Percentage of Nk Cells and Th 17 Cells in Rat That Received Izoniazid and Rifampycin
title_short The Effects of Aloe Vera on TNF-a Levels, the Percentage of Nk Cells and Th 17 Cells in Rat That Received Izoniazid and Rifampycin
title_sort effects of aloe vera on tnf-a levels, the percentage of nk cells and th 17 cells in rat that received izoniazid and rifampycin
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5723184/
https://www.ncbi.nlm.nih.gov/pubmed/29284895
http://dx.doi.org/10.5455/medarh.2017.71.308-311
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