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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...

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Autores principales: Al-Dabbagh, Bayan, Elhaty, Ismail A., Elhaw, Mohamed, Murali, Chandraprabha, Al Mansoori, Ameera, Awad, Basma, Amin, Amr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
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.
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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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