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Asteraceae Artemisia campestris and Artemisia herba-alba Essential Oils Trigger Apoptosis and Cell Cycle Arrest in Leishmania infantum Promastigotes
We report the chemical composition and anti-Leishmania and antioxidant activity of Artemisia campestris L. and Artemisia herba-alba Asso. essential oils (EOs). Our results showed that these extracts exhibit different antioxidant activities according to the used assay. The radical scavenging effects...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5078739/ https://www.ncbi.nlm.nih.gov/pubmed/27807464 http://dx.doi.org/10.1155/2016/9147096 |
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author | Aloui, Zohra Messaoud, Chokri Haoues, Meriam Neffati, Noura Bassoumi Jamoussi, Imen Essafi-Benkhadir, Khadija Boussaid, Mohamed Guizani, Ikram Karoui, Habib |
author_facet | Aloui, Zohra Messaoud, Chokri Haoues, Meriam Neffati, Noura Bassoumi Jamoussi, Imen Essafi-Benkhadir, Khadija Boussaid, Mohamed Guizani, Ikram Karoui, Habib |
author_sort | Aloui, Zohra |
collection | PubMed |
description | We report the chemical composition and anti-Leishmania and antioxidant activity of Artemisia campestris L. and Artemisia herba-alba Asso. essential oils (EOs). Our results showed that these extracts exhibit different antioxidant activities according to the used assay. The radical scavenging effects determined by DPPH assay were of IC(50) = 3.3 mg/mL and IC(50) = 9.1 mg/mL for Artemisia campestris and Artemisia herba-alba essential oils, respectively. However, antioxidant effects of both essential oils, determined by ferric-reducing antioxidant power (FRAP) assay, were in the same range (2.3 and 2.97 mg eq EDTA/g EO, resp.), while the Artemisia herba-alba essential oil showed highest chelating activity of Fe(2+) ions (27.48 mM Fe(2+)). Interestingly, we showed that both EOs possess dose-dependent activity against Leishmania infantum promastigotes with IC(50) values of 68 μg/mL and 44 μg/mL for A. herba-alba and A. campestris, respectively. We reported, for the first time, that antileishmanial activity of both EOs was mediated by cell apoptosis induction and cell cycle arrest at the sub-G0/G1 phase. All our results showed that EOs from A. herba-alba and A. campestris plants are promising candidates as anti-Leishmania medicinal products. |
format | Online Article Text |
id | pubmed-5078739 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-50787392016-11-02 Asteraceae Artemisia campestris and Artemisia herba-alba Essential Oils Trigger Apoptosis and Cell Cycle Arrest in Leishmania infantum Promastigotes Aloui, Zohra Messaoud, Chokri Haoues, Meriam Neffati, Noura Bassoumi Jamoussi, Imen Essafi-Benkhadir, Khadija Boussaid, Mohamed Guizani, Ikram Karoui, Habib Evid Based Complement Alternat Med Research Article We report the chemical composition and anti-Leishmania and antioxidant activity of Artemisia campestris L. and Artemisia herba-alba Asso. essential oils (EOs). Our results showed that these extracts exhibit different antioxidant activities according to the used assay. The radical scavenging effects determined by DPPH assay were of IC(50) = 3.3 mg/mL and IC(50) = 9.1 mg/mL for Artemisia campestris and Artemisia herba-alba essential oils, respectively. However, antioxidant effects of both essential oils, determined by ferric-reducing antioxidant power (FRAP) assay, were in the same range (2.3 and 2.97 mg eq EDTA/g EO, resp.), while the Artemisia herba-alba essential oil showed highest chelating activity of Fe(2+) ions (27.48 mM Fe(2+)). Interestingly, we showed that both EOs possess dose-dependent activity against Leishmania infantum promastigotes with IC(50) values of 68 μg/mL and 44 μg/mL for A. herba-alba and A. campestris, respectively. We reported, for the first time, that antileishmanial activity of both EOs was mediated by cell apoptosis induction and cell cycle arrest at the sub-G0/G1 phase. All our results showed that EOs from A. herba-alba and A. campestris plants are promising candidates as anti-Leishmania medicinal products. Hindawi Publishing Corporation 2016 2016-10-11 /pmc/articles/PMC5078739/ /pubmed/27807464 http://dx.doi.org/10.1155/2016/9147096 Text en Copyright © 2016 Zohra Aloui et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Aloui, Zohra Messaoud, Chokri Haoues, Meriam Neffati, Noura Bassoumi Jamoussi, Imen Essafi-Benkhadir, Khadija Boussaid, Mohamed Guizani, Ikram Karoui, Habib Asteraceae Artemisia campestris and Artemisia herba-alba Essential Oils Trigger Apoptosis and Cell Cycle Arrest in Leishmania infantum Promastigotes |
title | Asteraceae Artemisia campestris and Artemisia herba-alba Essential Oils Trigger Apoptosis and Cell Cycle Arrest in Leishmania infantum Promastigotes |
title_full | Asteraceae Artemisia campestris and Artemisia herba-alba Essential Oils Trigger Apoptosis and Cell Cycle Arrest in Leishmania infantum Promastigotes |
title_fullStr | Asteraceae Artemisia campestris and Artemisia herba-alba Essential Oils Trigger Apoptosis and Cell Cycle Arrest in Leishmania infantum Promastigotes |
title_full_unstemmed | Asteraceae Artemisia campestris and Artemisia herba-alba Essential Oils Trigger Apoptosis and Cell Cycle Arrest in Leishmania infantum Promastigotes |
title_short | Asteraceae Artemisia campestris and Artemisia herba-alba Essential Oils Trigger Apoptosis and Cell Cycle Arrest in Leishmania infantum Promastigotes |
title_sort | asteraceae artemisia campestris and artemisia herba-alba essential oils trigger apoptosis and cell cycle arrest in leishmania infantum promastigotes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5078739/ https://www.ncbi.nlm.nih.gov/pubmed/27807464 http://dx.doi.org/10.1155/2016/9147096 |
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