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Activity of Compounds from Temperate Propolis against Trypanosoma brucei and Leishmania mexicana
Ethanolic extracts of samples of temperate zone propolis, four from the UK and one from Poland, were tested against three Trypanosoma brucei strains and displayed EC(50) values < 20 µg/mL. The extracts were fractionated, from which 12 compounds and one two-component mixture were isolated, and cha...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8272135/ https://www.ncbi.nlm.nih.gov/pubmed/34206940 http://dx.doi.org/10.3390/molecules26133912 |
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author | Alotaibi, Adullah Ebiloma, Godwin U. Williams, Roderick Alfayez, Ibrahim A. Natto, Manal J. Alenezi, Sameah Siheri, Weam AlQarni, Malik Igoli, John O. Fearnley, James De Koning, Harry P. Watson, David G. |
author_facet | Alotaibi, Adullah Ebiloma, Godwin U. Williams, Roderick Alfayez, Ibrahim A. Natto, Manal J. Alenezi, Sameah Siheri, Weam AlQarni, Malik Igoli, John O. Fearnley, James De Koning, Harry P. Watson, David G. |
author_sort | Alotaibi, Adullah |
collection | PubMed |
description | Ethanolic extracts of samples of temperate zone propolis, four from the UK and one from Poland, were tested against three Trypanosoma brucei strains and displayed EC(50) values < 20 µg/mL. The extracts were fractionated, from which 12 compounds and one two-component mixture were isolated, and characterized by NMR and high-resolution mass spectrometry, as 3-acetoxypinobanksin, tectochrysin, kaempferol, pinocembrin, 4′-methoxykaempferol, galangin, chrysin, apigenin, pinostrobin, cinnamic acid, coumaric acid, cinnamyl ester/coumaric acid benzyl ester (mixture), 4′,7-dimethoxykaempferol, and naringenin 4′,7-dimethyl ether. The isolated compounds were tested against drug-sensitive and drug-resistant strains of T. brucei and Leishmania mexicana, with the highest activities ≤ 15 µM. The most active compounds against T. brucei were naringenin 4′,7 dimethyl ether and 4′methoxy kaempferol with activity of 15–20 µM against the three T. brucei strains. The most active compounds against L. mexicana were 4′,7-dimethoxykaempferol and the coumaric acid ester mixture, with EC(50) values of 12.9 ± 3.7 µM and 13.1 ± 1.0 µM. No loss of activity was found with the diamidine- and arsenical-resistant or phenanthridine-resistant T. brucei strains, or the miltefosine-resistant L. mexicana strain; no clear structure activity relationship was observed for the isolated compounds. Temperate propolis yields multiple compounds with anti-kinetoplastid activity. |
format | Online Article Text |
id | pubmed-8272135 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-82721352021-07-11 Activity of Compounds from Temperate Propolis against Trypanosoma brucei and Leishmania mexicana Alotaibi, Adullah Ebiloma, Godwin U. Williams, Roderick Alfayez, Ibrahim A. Natto, Manal J. Alenezi, Sameah Siheri, Weam AlQarni, Malik Igoli, John O. Fearnley, James De Koning, Harry P. Watson, David G. Molecules Article Ethanolic extracts of samples of temperate zone propolis, four from the UK and one from Poland, were tested against three Trypanosoma brucei strains and displayed EC(50) values < 20 µg/mL. The extracts were fractionated, from which 12 compounds and one two-component mixture were isolated, and characterized by NMR and high-resolution mass spectrometry, as 3-acetoxypinobanksin, tectochrysin, kaempferol, pinocembrin, 4′-methoxykaempferol, galangin, chrysin, apigenin, pinostrobin, cinnamic acid, coumaric acid, cinnamyl ester/coumaric acid benzyl ester (mixture), 4′,7-dimethoxykaempferol, and naringenin 4′,7-dimethyl ether. The isolated compounds were tested against drug-sensitive and drug-resistant strains of T. brucei and Leishmania mexicana, with the highest activities ≤ 15 µM. The most active compounds against T. brucei were naringenin 4′,7 dimethyl ether and 4′methoxy kaempferol with activity of 15–20 µM against the three T. brucei strains. The most active compounds against L. mexicana were 4′,7-dimethoxykaempferol and the coumaric acid ester mixture, with EC(50) values of 12.9 ± 3.7 µM and 13.1 ± 1.0 µM. No loss of activity was found with the diamidine- and arsenical-resistant or phenanthridine-resistant T. brucei strains, or the miltefosine-resistant L. mexicana strain; no clear structure activity relationship was observed for the isolated compounds. Temperate propolis yields multiple compounds with anti-kinetoplastid activity. MDPI 2021-06-26 /pmc/articles/PMC8272135/ /pubmed/34206940 http://dx.doi.org/10.3390/molecules26133912 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Alotaibi, Adullah Ebiloma, Godwin U. Williams, Roderick Alfayez, Ibrahim A. Natto, Manal J. Alenezi, Sameah Siheri, Weam AlQarni, Malik Igoli, John O. Fearnley, James De Koning, Harry P. Watson, David G. Activity of Compounds from Temperate Propolis against Trypanosoma brucei and Leishmania mexicana |
title | Activity of Compounds from Temperate Propolis against Trypanosoma brucei and Leishmania mexicana |
title_full | Activity of Compounds from Temperate Propolis against Trypanosoma brucei and Leishmania mexicana |
title_fullStr | Activity of Compounds from Temperate Propolis against Trypanosoma brucei and Leishmania mexicana |
title_full_unstemmed | Activity of Compounds from Temperate Propolis against Trypanosoma brucei and Leishmania mexicana |
title_short | Activity of Compounds from Temperate Propolis against Trypanosoma brucei and Leishmania mexicana |
title_sort | activity of compounds from temperate propolis against trypanosoma brucei and leishmania mexicana |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8272135/ https://www.ncbi.nlm.nih.gov/pubmed/34206940 http://dx.doi.org/10.3390/molecules26133912 |
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