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Phytochemical screening, antioxidant, antityrosinase, and antigenotoxic potential of Amaranthus viridis extract

OBJECTIVE: Amaranthus viridis (Amaranthaceae) widely distributed all over the world, growing under a wide range of climatic conditions and has been utilized as a medicinal herb in traditional Ayurvedic medicine as antipyretic agents, also for the treatment of inflammation, ulcer, diabetic, asthma an...

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Autores principales: Kumari, Sima, Elancheran, R., Devi, Rajlakshmi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6106121/
https://www.ncbi.nlm.nih.gov/pubmed/30166750
http://dx.doi.org/10.4103/ijp.IJP_77_18
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author Kumari, Sima
Elancheran, R.
Devi, Rajlakshmi
author_facet Kumari, Sima
Elancheran, R.
Devi, Rajlakshmi
author_sort Kumari, Sima
collection PubMed
description OBJECTIVE: Amaranthus viridis (Amaranthaceae) widely distributed all over the world, growing under a wide range of climatic conditions and has been utilized as a medicinal herb in traditional Ayurvedic medicine as antipyretic agents, also for the treatment of inflammation, ulcer, diabetic, asthma and hyperlipidemia. The aim of the study was designed to evaluate the chemical composition and antioxidant and biological properties of different fractions obtained from A. viridis. MATERIALS AND METHODS: Four different extracts of A. viridis were prepared using aqueous, methanol, chloroform, and hexane and investigated their antioxidant potential using free radical scavenging activities such as 2,2-diphenyl-1-picrylhydrazyl (DPPH), 2,2'-azinobis-3-ethylbenzothiazoline-6-sulfonic acid (ABTS), and nitric oxide (NO) radical scavenging activity, as well as metal chelating activity. In addition, antityrosinase and antigenotoxicity properties were also evaluated by the standard in vitro methods. Finally, the active methanolic extract (ME) was investigated for identifying the phenolic compounds using UPLC-MS/MS. RESULTS: In the present study, chlorogenic acid, gulonic acid, and kaempferol were found to be the major components responsible for the antioxidant activity of A. viridis extract as evidenced from UPLC-MS/MS. Furthermore, the ME of A. viridis revealed excellent antioxidant activities such as DPPH radical scavenging activity (IC(50)= 47.23 ± 0.66 μg/mL), NO radical scavenging activity (IC(50)= 64.33 ± 2.01 μg/mL), hydrogen peroxide (H(2)O(2)) radical scavenging activity (IC(50)= 33.21 ± 3.3 μg/mL), ABTS radical scavenging activity (IC(50)= 47.61 ± 1.31 μg/mL), metal chelating activity (IC(50)= 32.1 ± 1.11 μg/mL), as well as lipid peroxidation inhibiting activity (IC(50)= 112 ± 1.21 μg/mL). Furthermore, ME revealed that the protective effects of extract were observed on H(2)O(2)-induced DNA damages with alkaline comet assay. CONCLUSIONS: Taken together, the study concluded that the promising antioxidant capacities of A. viridis extract can further be utilized in various agricultural, pharmaceutical, and food applications.
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spelling pubmed-61061212018-08-30 Phytochemical screening, antioxidant, antityrosinase, and antigenotoxic potential of Amaranthus viridis extract Kumari, Sima Elancheran, R. Devi, Rajlakshmi Indian J Pharmacol Research Article OBJECTIVE: Amaranthus viridis (Amaranthaceae) widely distributed all over the world, growing under a wide range of climatic conditions and has been utilized as a medicinal herb in traditional Ayurvedic medicine as antipyretic agents, also for the treatment of inflammation, ulcer, diabetic, asthma and hyperlipidemia. The aim of the study was designed to evaluate the chemical composition and antioxidant and biological properties of different fractions obtained from A. viridis. MATERIALS AND METHODS: Four different extracts of A. viridis were prepared using aqueous, methanol, chloroform, and hexane and investigated their antioxidant potential using free radical scavenging activities such as 2,2-diphenyl-1-picrylhydrazyl (DPPH), 2,2'-azinobis-3-ethylbenzothiazoline-6-sulfonic acid (ABTS), and nitric oxide (NO) radical scavenging activity, as well as metal chelating activity. In addition, antityrosinase and antigenotoxicity properties were also evaluated by the standard in vitro methods. Finally, the active methanolic extract (ME) was investigated for identifying the phenolic compounds using UPLC-MS/MS. RESULTS: In the present study, chlorogenic acid, gulonic acid, and kaempferol were found to be the major components responsible for the antioxidant activity of A. viridis extract as evidenced from UPLC-MS/MS. Furthermore, the ME of A. viridis revealed excellent antioxidant activities such as DPPH radical scavenging activity (IC(50)= 47.23 ± 0.66 μg/mL), NO radical scavenging activity (IC(50)= 64.33 ± 2.01 μg/mL), hydrogen peroxide (H(2)O(2)) radical scavenging activity (IC(50)= 33.21 ± 3.3 μg/mL), ABTS radical scavenging activity (IC(50)= 47.61 ± 1.31 μg/mL), metal chelating activity (IC(50)= 32.1 ± 1.11 μg/mL), as well as lipid peroxidation inhibiting activity (IC(50)= 112 ± 1.21 μg/mL). Furthermore, ME revealed that the protective effects of extract were observed on H(2)O(2)-induced DNA damages with alkaline comet assay. CONCLUSIONS: Taken together, the study concluded that the promising antioxidant capacities of A. viridis extract can further be utilized in various agricultural, pharmaceutical, and food applications. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC6106121/ /pubmed/30166750 http://dx.doi.org/10.4103/ijp.IJP_77_18 Text en Copyright: © 2018 Indian Journal of Pharmacology http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Research Article
Kumari, Sima
Elancheran, R.
Devi, Rajlakshmi
Phytochemical screening, antioxidant, antityrosinase, and antigenotoxic potential of Amaranthus viridis extract
title Phytochemical screening, antioxidant, antityrosinase, and antigenotoxic potential of Amaranthus viridis extract
title_full Phytochemical screening, antioxidant, antityrosinase, and antigenotoxic potential of Amaranthus viridis extract
title_fullStr Phytochemical screening, antioxidant, antityrosinase, and antigenotoxic potential of Amaranthus viridis extract
title_full_unstemmed Phytochemical screening, antioxidant, antityrosinase, and antigenotoxic potential of Amaranthus viridis extract
title_short Phytochemical screening, antioxidant, antityrosinase, and antigenotoxic potential of Amaranthus viridis extract
title_sort phytochemical screening, antioxidant, antityrosinase, and antigenotoxic potential of amaranthus viridis extract
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6106121/
https://www.ncbi.nlm.nih.gov/pubmed/30166750
http://dx.doi.org/10.4103/ijp.IJP_77_18
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