Evaluation of the Anti-Trypanosomal Activity of Vietnamese Essential Oils, with Emphasis on Curcuma longa L. and Its Components
Human African trypanosomiasis (HAT), known as sleeping sickness and caused by , is threatening low-income populations in sub-Saharan African countries with 61 million people at risk of infection. In order to discover new natural products against HAT, thirty-seven Vietnamese essential oils (EOs) were...
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Published in | Molecules (Basel, Switzerland) Vol. 24; no. 6; p. 1158 |
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Main Authors | , , , , , |
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Language | English |
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Abstract | Human African trypanosomiasis (HAT), known as sleeping sickness and caused by
, is threatening low-income populations in sub-Saharan African countries with 61 million people at risk of infection. In order to discover new natural products against HAT, thirty-seven Vietnamese essential oils (EOs) were screened for their activity in vitro on
(
) and cytotoxicity on mammalian cells (WI38, J774). Based on the selectivity indices (SIs), the more active and selective EOs were analyzed by gas chromatography. The anti-trypanosomal activity and cytotoxicity of some major compounds (isolated or commercial) were also determined. Our results showed for the first time the selective anti-trypanosomal effect of four EOs, extracted from three Zingiberaceae species (
,
, and
) and one Lauraceae species (
) with IC
values of 3.17 ± 0.72, 2.51 ± 1.08, 3.10 ± 0.08, and 2.67 ± 1.12 nL/mL respectively and SI > 10. Identified compounds accounted for more than 85% for each of them. Among the five major components of
EO, curlone is the most promising anti-trypanosomal candidate with an IC
of 1.38 ± 0.45 µg/mL and SIs of 31.7 and 18.2 compared to WI38 and J774 respectively. |
---|---|
AbstractList | Human African trypanosomiasis (HAT), known as sleeping sickness and caused by
, is threatening low-income populations in sub-Saharan African countries with 61 million people at risk of infection. In order to discover new natural products against HAT, thirty-seven Vietnamese essential oils (EOs) were screened for their activity in vitro on
(
) and cytotoxicity on mammalian cells (WI38, J774). Based on the selectivity indices (SIs), the more active and selective EOs were analyzed by gas chromatography. The anti-trypanosomal activity and cytotoxicity of some major compounds (isolated or commercial) were also determined. Our results showed for the first time the selective anti-trypanosomal effect of four EOs, extracted from three Zingiberaceae species (
,
, and
) and one Lauraceae species (
) with IC
values of 3.17 ± 0.72, 2.51 ± 1.08, 3.10 ± 0.08, and 2.67 ± 1.12 nL/mL respectively and SI > 10. Identified compounds accounted for more than 85% for each of them. Among the five major components of
EO, curlone is the most promising anti-trypanosomal candidate with an IC
of 1.38 ± 0.45 µg/mL and SIs of 31.7 and 18.2 compared to WI38 and J774 respectively. Human African trypanosomiasis (HAT), known as sleeping sickness and caused by Trypanosoma brucei , is threatening low-income populations in sub-Saharan African countries with 61 million people at risk of infection. In order to discover new natural products against HAT, thirty-seven Vietnamese essential oils (EOs) were screened for their activity in vitro on Trypanosoma brucei brucei ( Tbb ) and cytotoxicity on mammalian cells (WI38, J774). Based on the selectivity indices (SIs), the more active and selective EOs were analyzed by gas chromatography. The anti-trypanosomal activity and cytotoxicity of some major compounds (isolated or commercial) were also determined. Our results showed for the first time the selective anti-trypanosomal effect of four EOs, extracted from three Zingiberaceae species ( Curcuma longa , Curcuma zedoaria , and Zingiber officinale ) and one Lauraceae species ( Litsea cubeba ) with IC 50 values of 3.17 ± 0.72, 2.51 ± 1.08, 3.10 ± 0.08, and 2.67 ± 1.12 nL/mL respectively and SI > 10. Identified compounds accounted for more than 85% for each of them. Among the five major components of Curcuma longa EO, curlone is the most promising anti-trypanosomal candidate with an IC 50 of 1.38 ± 0.45 µg/mL and SIs of 31.7 and 18.2 compared to WI38 and J774 respectively. Human African trypanosomiasis (HAT), known as sleeping sickness and caused by Trypanosoma brucei, is threatening low-income populations in sub-Saharan African countries with 61 million people at risk of infection. In order to discover new natural products against HAT, thirty-seven Vietnamese essential oils (EOs) were screened for their activity in vitro on Trypanosoma brucei brucei (Tbb) and cytotoxicity on mammalian cells (WI38, J774). Based on the selectivity indices (SIs), the more active and selective EOs were analyzed by gas chromatography. The anti-trypanosomal activity and cytotoxicity of some major compounds (isolated or commercial) were also determined. Our results showed for the first time the selective anti-trypanosomal effect of four EOs, extracted from three Zingiberaceae species (Curcuma longa, Curcuma zedoaria, and Zingiber officinale) and one Lauraceae species (Litsea cubeba) with IC50 values of 3.17 ± 0.72, 2.51 ± 1.08, 3.10 ± 0.08, and 2.67 ± 1.12 nL/mL respectively and SI > 10. Identified compounds accounted for more than 85% for each of them. Among the five major components of Curcuma longa EO, curlone is the most promising anti-trypanosomal candidate with an IC50 of 1.38 ± 0.45 µg/mL and SIs of 31.7 and 18.2 compared to WI38 and J774 respectively. Human African trypanosomiasis (HAT), known as sleeping sickness and caused by Trypanosoma brucei, is threatening low-income populations in sub-Saharan African countries with 61 million people at risk of infection. In order to discover new natural products against HAT, thirty-seven Vietnamese essential oils (EOs) were screened for their activity in vitro on Trypanosoma brucei brucei (Tbb) and cytotoxicity on mammalian cells (WI38, J774). Based on the selectivity indices (SIs), the more active and selective EOs were analyzed by gas chromatography. The anti-trypanosomal activity and cytotoxicity of some major compounds (isolated or commercial) were also determined. Our results showed for the first time the selective anti-trypanosomal effect of four EOs, extracted from three Zingiberaceae species (Curcuma longa, Curcuma zedoaria, and Zingiber officinale) and one Lauraceae species (Litsea cubeba) with IC50 values of 3.17 ± 0.72, 2.51 ± 1.08, 3.10 ± 0.08, and 2.67 ± 1.12 nL/mL respectively and SI > 10. Identified compounds accounted for more than 85% for each of them. Among the five major components of Curcuma longa EO, curlone is the most promising anti-trypanosomal candidate with an IC50 of 1.38 ± 0.45 µg/mL and SIs of 31.7 and 18.2 compared to WI38 and J774 respectively. |
Author | Nghiem, Duc Trong Quetin-Leclercq, Joëlle Beaufay, Claire Mingeot-Leclercq, Marie-Paule Pham, Tuan Anh Le, Thanh Binh |
AuthorAffiliation | 2 Department of Pharmacognosy, Hanoi University of Pharmacy, 13-15 Le Thanh Tong, Hoan Kiem, Hanoi 100000, Vietnam; tuananhpharm@hup.edu.vn 4 TFAR Research Group, Louvain Drug Research Institute, Université catholique de Louvain, UCLouvain, 1200 Bruxelles, Belgium; marie-paule.mingeot@uclouvain.be 3 Department of Botany, Hanoi University of Pharmacy, 13-15 Le Thanh Tong, Hoan Kiem, Hanoi 100000, Vietnam; ductrongeb@hup.edu.vn 1 GNOS Research Group, Louvain Drug Research Institute, Université catholique de Louvain, UCLouvain, 1200 Bruxelles, Belgium; claire.beaufay@uclouvain.be |
AuthorAffiliation_xml | – name: 2 Department of Pharmacognosy, Hanoi University of Pharmacy, 13-15 Le Thanh Tong, Hoan Kiem, Hanoi 100000, Vietnam; tuananhpharm@hup.edu.vn – name: 4 TFAR Research Group, Louvain Drug Research Institute, Université catholique de Louvain, UCLouvain, 1200 Bruxelles, Belgium; marie-paule.mingeot@uclouvain.be – name: 1 GNOS Research Group, Louvain Drug Research Institute, Université catholique de Louvain, UCLouvain, 1200 Bruxelles, Belgium; claire.beaufay@uclouvain.be – name: 3 Department of Botany, Hanoi University of Pharmacy, 13-15 Le Thanh Tong, Hoan Kiem, Hanoi 100000, Vietnam; ductrongeb@hup.edu.vn |
Author_xml | – sequence: 1 givenname: Thanh Binh orcidid: 0000-0002-2895-1508 surname: Le fullname: Le, Thanh Binh email: thanh.le@uclouvain.be, thanh.le@uclouvain.be organization: Department of Pharmacognosy, Hanoi University of Pharmacy, 13-15 Le Thanh Tong, Hoan Kiem, Hanoi 100000, Vietnam. thanh.le@uclouvain.be – sequence: 2 givenname: Claire orcidid: 0000-0002-0942-4649 surname: Beaufay fullname: Beaufay, Claire email: claire.beaufay@uclouvain.be organization: GNOS Research Group, Louvain Drug Research Institute, Université catholique de Louvain, UCLouvain, 1200 Bruxelles, Belgium. claire.beaufay@uclouvain.be – sequence: 3 givenname: Duc Trong orcidid: 0000-0003-2381-6144 surname: Nghiem fullname: Nghiem, Duc Trong email: ductrongeb@hup.edu.vn organization: Department of Botany, Hanoi University of Pharmacy, 13-15 Le Thanh Tong, Hoan Kiem, Hanoi 100000, Vietnam. ductrongeb@hup.edu.vn – sequence: 4 givenname: Tuan Anh surname: Pham fullname: Pham, Tuan Anh email: tuananhpharm@hup.edu.vn organization: Department of Pharmacognosy, Hanoi University of Pharmacy, 13-15 Le Thanh Tong, Hoan Kiem, Hanoi 100000, Vietnam. tuananhpharm@hup.edu.vn – sequence: 5 givenname: Marie-Paule surname: Mingeot-Leclercq fullname: Mingeot-Leclercq, Marie-Paule email: marie-paule.mingeot@uclouvain.be organization: TFAR Research Group, Louvain Drug Research Institute, Université catholique de Louvain, UCLouvain, 1200 Bruxelles, Belgium. marie-paule.mingeot@uclouvain.be – sequence: 6 givenname: Joëlle orcidid: 0000-0002-2278-6206 surname: Quetin-Leclercq fullname: Quetin-Leclercq, Joëlle email: joelle.leclercq@uclouvain.be organization: GNOS Research Group, Louvain Drug Research Institute, Université catholique de Louvain, UCLouvain, 1200 Bruxelles, Belgium. joelle.leclercq@uclouvain.be |
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Copyright | 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. 2019 by the authors. 2019 |
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Keywords | Curcuma zedoaria Trypanosoma Curcuma longa Litsea cubeba α-zingiberene, β-sesquiphellandrene ar-turmerone, curlone Zingiber officinale ar-curcumene |
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Snippet | Human African trypanosomiasis (HAT), known as sleeping sickness and caused by
, is threatening low-income populations in sub-Saharan African countries with 61... Human African trypanosomiasis (HAT), known as sleeping sickness and caused by Trypanosoma brucei, is threatening low-income populations in sub-Saharan African... Human African trypanosomiasis (HAT), known as sleeping sickness and caused by Trypanosoma brucei , is threatening low-income populations in sub-Saharan African... |
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SubjectTerms | African trypanosomiasis ar-curcumene ar-turmerone, curlone Chromatography Curcuma longa Curcuma zedoaria Cytotoxicity Essential oils Gas chromatography Ginger Health risks Litsea cubeba Mammalian cells Natural products Oils & fats Parasites Selectivity Trypanosoma Trypanosoma brucei Vector-borne diseases Zingiber officinale α-zingiberene, β-sesquiphellandrene |
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Title | Evaluation of the Anti-Trypanosomal Activity of Vietnamese Essential Oils, with Emphasis on Curcuma longa L. and Its Components |
URI | https://www.ncbi.nlm.nih.gov/pubmed/30909559 https://www.proquest.com/docview/2548931569 https://search.proquest.com/docview/2197886796 https://pubmed.ncbi.nlm.nih.gov/PMC6471621 https://doaj.org/article/ef25ba067c7b48f5ae63f1f014765791 |
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