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Free radical scavenging ability of Aspalathus linearis in two in vitro models of diabetes and cancer

The free radical scavenging activity of Aspalathus linearis (Rooibos tea) and its effect on reactive oxygen species (ROS), catalase (CAT), and superoxide dismutase (SOD) were investigated in two in vitro disease models of cancer and diabetes. Although the antioxidant activity of this tea has been re...

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Autores principales: Waisundara, Viduranga Y., Hoon, Lee Yian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4488559/
https://www.ncbi.nlm.nih.gov/pubmed/26151031
http://dx.doi.org/10.1016/j.jtcme.2014.11.009
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author Waisundara, Viduranga Y.
Hoon, Lee Yian
author_facet Waisundara, Viduranga Y.
Hoon, Lee Yian
author_sort Waisundara, Viduranga Y.
collection PubMed
description The free radical scavenging activity of Aspalathus linearis (Rooibos tea) and its effect on reactive oxygen species (ROS), catalase (CAT), and superoxide dismutase (SOD) were investigated in two in vitro disease models of cancer and diabetes. Although the antioxidant activity of this tea has been reported in several studies, its effects in disease models of ROS-induced oxidative stress have not been systematically evaluated to date. The oxygen radical absorbance capacity (ORAC) assay was used in this study to quantify the antioxidant capacity of the extract, whereas the ROS scavenging ability in hyperglycemia-induced human umbilical vein endothelial cells (HUVECs) and HeLa cells were investigated. The CAT and SOD assays were also carried out in the two disease models in order to evaluate the effect of the extract in the stimulation of these two enzyme activities. The extract was observed to have reduced ROS in a dose-dependent manner in both HUVECs and HeLa cells. The stimulation of the CAT and SOD enzyme activities were observed to be dose-dependent as well. The high ORAC value of the extract indicated the presence of antioxidant compounds which could directly quench ROS, whereby this mechanism of action could be hypothesized to have been further complemented through the stimulation of CAT and SOD. Overall, the Aspalathus linearis extract was observed to have increased the CAT and SOD activities in two in vitro disease models of cancer and hyperglycemia. Given the correlation between the ORAC values, the increases in CAT and SOD activities and the reduction in ROS in a dose-dependent manner, it could be hypothesized that the extract had a significant therapeutic potential for either the prevention of the onset of the two diseases or their progression because ROS has been identified as their root causes.
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spelling pubmed-44885592015-07-06 Free radical scavenging ability of Aspalathus linearis in two in vitro models of diabetes and cancer Waisundara, Viduranga Y. Hoon, Lee Yian J Tradit Complement Med Short Communication The free radical scavenging activity of Aspalathus linearis (Rooibos tea) and its effect on reactive oxygen species (ROS), catalase (CAT), and superoxide dismutase (SOD) were investigated in two in vitro disease models of cancer and diabetes. Although the antioxidant activity of this tea has been reported in several studies, its effects in disease models of ROS-induced oxidative stress have not been systematically evaluated to date. The oxygen radical absorbance capacity (ORAC) assay was used in this study to quantify the antioxidant capacity of the extract, whereas the ROS scavenging ability in hyperglycemia-induced human umbilical vein endothelial cells (HUVECs) and HeLa cells were investigated. The CAT and SOD assays were also carried out in the two disease models in order to evaluate the effect of the extract in the stimulation of these two enzyme activities. The extract was observed to have reduced ROS in a dose-dependent manner in both HUVECs and HeLa cells. The stimulation of the CAT and SOD enzyme activities were observed to be dose-dependent as well. The high ORAC value of the extract indicated the presence of antioxidant compounds which could directly quench ROS, whereby this mechanism of action could be hypothesized to have been further complemented through the stimulation of CAT and SOD. Overall, the Aspalathus linearis extract was observed to have increased the CAT and SOD activities in two in vitro disease models of cancer and hyperglycemia. Given the correlation between the ORAC values, the increases in CAT and SOD activities and the reduction in ROS in a dose-dependent manner, it could be hypothesized that the extract had a significant therapeutic potential for either the prevention of the onset of the two diseases or their progression because ROS has been identified as their root causes. Elsevier 2015-01-20 /pmc/articles/PMC4488559/ /pubmed/26151031 http://dx.doi.org/10.1016/j.jtcme.2014.11.009 Text en Copyright © 2014, Center for Food and Biomolecules, National Taiwan University. Production and hosting by Elsevier Taiwan LLC. All rights reserved. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
spellingShingle Short Communication
Waisundara, Viduranga Y.
Hoon, Lee Yian
Free radical scavenging ability of Aspalathus linearis in two in vitro models of diabetes and cancer
title Free radical scavenging ability of Aspalathus linearis in two in vitro models of diabetes and cancer
title_full Free radical scavenging ability of Aspalathus linearis in two in vitro models of diabetes and cancer
title_fullStr Free radical scavenging ability of Aspalathus linearis in two in vitro models of diabetes and cancer
title_full_unstemmed Free radical scavenging ability of Aspalathus linearis in two in vitro models of diabetes and cancer
title_short Free radical scavenging ability of Aspalathus linearis in two in vitro models of diabetes and cancer
title_sort free radical scavenging ability of aspalathus linearis in two in vitro models of diabetes and cancer
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4488559/
https://www.ncbi.nlm.nih.gov/pubmed/26151031
http://dx.doi.org/10.1016/j.jtcme.2014.11.009
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