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Antioxidant and anticancer activities of chamomile (Matricaria recutita L.)
OBJECTIVES: The present study aimed at determining the antioxidant activity, total phenols and flavonoids and to evaluate the antiproliferative activity of ethanolic extract of Matricaria recutita L. (chamomile). The antioxidant activities were measured using the 2, 2-diphenyl-1-picrylhydrazyl (DPPH...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6317209/ https://www.ncbi.nlm.nih.gov/pubmed/30602390 http://dx.doi.org/10.1186/s13104-018-3960-y |
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author | Al-Dabbagh, Bayan Elhaty, Ismail A. Elhaw, Mohamed Murali, Chandraprabha Al Mansoori, Ameera Awad, Basma Amin, Amr |
author_facet | Al-Dabbagh, Bayan Elhaty, Ismail A. Elhaw, Mohamed Murali, Chandraprabha Al Mansoori, Ameera Awad, Basma Amin, Amr |
author_sort | Al-Dabbagh, Bayan |
collection | PubMed |
description | OBJECTIVES: The present study aimed at determining the antioxidant activity, total phenols and flavonoids and to evaluate the antiproliferative activity of ethanolic extract of Matricaria recutita L. (chamomile). The antioxidant activities were measured using the 2, 2-diphenyl-1-picrylhydrazyl (DPPH) assay. The total phenolic content was measured by the Folin–Ciocalteu assay. The flavonoid content was determined using the aluminum chloride method. The MTT assay was used to estimate the antiproliferative activities against human hepatoma (HepG2) cancer cell line. We assessed the mode of action of the extract as a cancer preventive agent and reported its ability to regulate tumor angiogenesis by down regulating in a dose dependent manner the expression of some proteins involved in the process. RESULTS: The percentage inhibition of DPPH scavenging activity was dose-dependent ranging between (94.8% ± 0.03) at 1.50 mg/mL and (84.2% ± 0.86) at 0.15 mg/mL. It showed high polyphenols (21.4 ± 0.327 mg GAE/g) and high flavonoids content (157.9 ± 2.22 mg QE/g). Effect of extract was investigated against HepG2 cells. A dose-dependent reduction in cell viability was recorded in cells treated with the extract. The IC(50) was ~ 300 µg/mL. It significantly inhibited the level of important prerequisite angiogenesis markers both in HepG2 cells and ex vivo. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13104-018-3960-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6317209 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63172092019-01-08 Antioxidant and anticancer activities of chamomile (Matricaria recutita L.) Al-Dabbagh, Bayan Elhaty, Ismail A. Elhaw, Mohamed Murali, Chandraprabha Al Mansoori, Ameera Awad, Basma Amin, Amr BMC Res Notes Research Note OBJECTIVES: The present study aimed at determining the antioxidant activity, total phenols and flavonoids and to evaluate the antiproliferative activity of ethanolic extract of Matricaria recutita L. (chamomile). The antioxidant activities were measured using the 2, 2-diphenyl-1-picrylhydrazyl (DPPH) assay. The total phenolic content was measured by the Folin–Ciocalteu assay. The flavonoid content was determined using the aluminum chloride method. The MTT assay was used to estimate the antiproliferative activities against human hepatoma (HepG2) cancer cell line. We assessed the mode of action of the extract as a cancer preventive agent and reported its ability to regulate tumor angiogenesis by down regulating in a dose dependent manner the expression of some proteins involved in the process. RESULTS: The percentage inhibition of DPPH scavenging activity was dose-dependent ranging between (94.8% ± 0.03) at 1.50 mg/mL and (84.2% ± 0.86) at 0.15 mg/mL. It showed high polyphenols (21.4 ± 0.327 mg GAE/g) and high flavonoids content (157.9 ± 2.22 mg QE/g). Effect of extract was investigated against HepG2 cells. A dose-dependent reduction in cell viability was recorded in cells treated with the extract. The IC(50) was ~ 300 µg/mL. It significantly inhibited the level of important prerequisite angiogenesis markers both in HepG2 cells and ex vivo. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13104-018-3960-y) contains supplementary material, which is available to authorized users. BioMed Central 2019-01-03 /pmc/articles/PMC6317209/ /pubmed/30602390 http://dx.doi.org/10.1186/s13104-018-3960-y Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Note Al-Dabbagh, Bayan Elhaty, Ismail A. Elhaw, Mohamed Murali, Chandraprabha Al Mansoori, Ameera Awad, Basma Amin, Amr Antioxidant and anticancer activities of chamomile (Matricaria recutita L.) |
title | Antioxidant and anticancer activities of chamomile (Matricaria recutita L.) |
title_full | Antioxidant and anticancer activities of chamomile (Matricaria recutita L.) |
title_fullStr | Antioxidant and anticancer activities of chamomile (Matricaria recutita L.) |
title_full_unstemmed | Antioxidant and anticancer activities of chamomile (Matricaria recutita L.) |
title_short | Antioxidant and anticancer activities of chamomile (Matricaria recutita L.) |
title_sort | antioxidant and anticancer activities of chamomile (matricaria recutita l.) |
topic | Research Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6317209/ https://www.ncbi.nlm.nih.gov/pubmed/30602390 http://dx.doi.org/10.1186/s13104-018-3960-y |
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