Cargando…

The Antiprotozoal Activity of Papua New Guinea Propolis and Its Triterpenes

Profiling a propolis sample from Papua New Guinea (PNG) using high-resolution mass spectrometry indicated that it contained several triterpenoids. Further fractionation by column chromatography and medium-pressure liquid chromatography (MPLC) followed by nuclear magnetic resonance spectroscopy (NMR)...

Descripción completa

Detalles Bibliográficos
Autores principales: Alenezi, Samya S., Alenezi, Naif D., Ebiloma, Godwin U., Natto, Manal J., Ungogo, Marzuq A., Igoli, John O., Ferro, Valerie A., Gray, Alexander I., Fearnley, James, de Koning, Harry P., Watson, David G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8911803/
https://www.ncbi.nlm.nih.gov/pubmed/35268726
http://dx.doi.org/10.3390/molecules27051622
_version_ 1784666927347531776
author Alenezi, Samya S.
Alenezi, Naif D.
Ebiloma, Godwin U.
Natto, Manal J.
Ungogo, Marzuq A.
Igoli, John O.
Ferro, Valerie A.
Gray, Alexander I.
Fearnley, James
de Koning, Harry P.
Watson, David G.
author_facet Alenezi, Samya S.
Alenezi, Naif D.
Ebiloma, Godwin U.
Natto, Manal J.
Ungogo, Marzuq A.
Igoli, John O.
Ferro, Valerie A.
Gray, Alexander I.
Fearnley, James
de Koning, Harry P.
Watson, David G.
author_sort Alenezi, Samya S.
collection PubMed
description Profiling a propolis sample from Papua New Guinea (PNG) using high-resolution mass spectrometry indicated that it contained several triterpenoids. Further fractionation by column chromatography and medium-pressure liquid chromatography (MPLC) followed by nuclear magnetic resonance spectroscopy (NMR) identified 12 triterpenoids. Five of these were obtained pure and the others as mixtures of two or three compounds. The compounds identified were: mangiferonic acid, ambonic acid, isomangiferolic acid, ambolic acid, 27-hydroxyisomangiferolic acid, cycloartenol, cycloeucalenol, 24-methylenecycloartenol, 20-hydroxybetulin, betulin, betulinic acid and madecassic acid. The fractions from the propolis and the purified compounds were tested in vitro against Crithidia fasciculata, Trypanosoma congolense, drug-resistant Trypanosoma congolense, Trypanosoma b. brucei and multidrug-resistant Trypanosoma b. brucei (B48). They were also assayed for their toxicity against U947 cells. The compounds and fractions displayed moderate to high activity against parasitic protozoa but only low cytotoxicity against the mammalian cells. The most active isolated compound, 20-hydroxybetulin, was found to be trypanostatic when different concentrations were tested against T. b. brucei growth.
format Online
Article
Text
id pubmed-8911803
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-89118032022-03-11 The Antiprotozoal Activity of Papua New Guinea Propolis and Its Triterpenes Alenezi, Samya S. Alenezi, Naif D. Ebiloma, Godwin U. Natto, Manal J. Ungogo, Marzuq A. Igoli, John O. Ferro, Valerie A. Gray, Alexander I. Fearnley, James de Koning, Harry P. Watson, David G. Molecules Article Profiling a propolis sample from Papua New Guinea (PNG) using high-resolution mass spectrometry indicated that it contained several triterpenoids. Further fractionation by column chromatography and medium-pressure liquid chromatography (MPLC) followed by nuclear magnetic resonance spectroscopy (NMR) identified 12 triterpenoids. Five of these were obtained pure and the others as mixtures of two or three compounds. The compounds identified were: mangiferonic acid, ambonic acid, isomangiferolic acid, ambolic acid, 27-hydroxyisomangiferolic acid, cycloartenol, cycloeucalenol, 24-methylenecycloartenol, 20-hydroxybetulin, betulin, betulinic acid and madecassic acid. The fractions from the propolis and the purified compounds were tested in vitro against Crithidia fasciculata, Trypanosoma congolense, drug-resistant Trypanosoma congolense, Trypanosoma b. brucei and multidrug-resistant Trypanosoma b. brucei (B48). They were also assayed for their toxicity against U947 cells. The compounds and fractions displayed moderate to high activity against parasitic protozoa but only low cytotoxicity against the mammalian cells. The most active isolated compound, 20-hydroxybetulin, was found to be trypanostatic when different concentrations were tested against T. b. brucei growth. MDPI 2022-03-01 /pmc/articles/PMC8911803/ /pubmed/35268726 http://dx.doi.org/10.3390/molecules27051622 Text en © 2022 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
Alenezi, Samya S.
Alenezi, Naif D.
Ebiloma, Godwin U.
Natto, Manal J.
Ungogo, Marzuq A.
Igoli, John O.
Ferro, Valerie A.
Gray, Alexander I.
Fearnley, James
de Koning, Harry P.
Watson, David G.
The Antiprotozoal Activity of Papua New Guinea Propolis and Its Triterpenes
title The Antiprotozoal Activity of Papua New Guinea Propolis and Its Triterpenes
title_full The Antiprotozoal Activity of Papua New Guinea Propolis and Its Triterpenes
title_fullStr The Antiprotozoal Activity of Papua New Guinea Propolis and Its Triterpenes
title_full_unstemmed The Antiprotozoal Activity of Papua New Guinea Propolis and Its Triterpenes
title_short The Antiprotozoal Activity of Papua New Guinea Propolis and Its Triterpenes
title_sort antiprotozoal activity of papua new guinea propolis and its triterpenes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8911803/
https://www.ncbi.nlm.nih.gov/pubmed/35268726
http://dx.doi.org/10.3390/molecules27051622
work_keys_str_mv AT alenezisamyas theantiprotozoalactivityofpapuanewguineapropolisanditstriterpenes
AT alenezinaifd theantiprotozoalactivityofpapuanewguineapropolisanditstriterpenes
AT ebilomagodwinu theantiprotozoalactivityofpapuanewguineapropolisanditstriterpenes
AT nattomanalj theantiprotozoalactivityofpapuanewguineapropolisanditstriterpenes
AT ungogomarzuqa theantiprotozoalactivityofpapuanewguineapropolisanditstriterpenes
AT igolijohno theantiprotozoalactivityofpapuanewguineapropolisanditstriterpenes
AT ferrovaleriea theantiprotozoalactivityofpapuanewguineapropolisanditstriterpenes
AT grayalexanderi theantiprotozoalactivityofpapuanewguineapropolisanditstriterpenes
AT fearnleyjames theantiprotozoalactivityofpapuanewguineapropolisanditstriterpenes
AT dekoningharryp theantiprotozoalactivityofpapuanewguineapropolisanditstriterpenes
AT watsondavidg theantiprotozoalactivityofpapuanewguineapropolisanditstriterpenes
AT alenezisamyas antiprotozoalactivityofpapuanewguineapropolisanditstriterpenes
AT alenezinaifd antiprotozoalactivityofpapuanewguineapropolisanditstriterpenes
AT ebilomagodwinu antiprotozoalactivityofpapuanewguineapropolisanditstriterpenes
AT nattomanalj antiprotozoalactivityofpapuanewguineapropolisanditstriterpenes
AT ungogomarzuqa antiprotozoalactivityofpapuanewguineapropolisanditstriterpenes
AT igolijohno antiprotozoalactivityofpapuanewguineapropolisanditstriterpenes
AT ferrovaleriea antiprotozoalactivityofpapuanewguineapropolisanditstriterpenes
AT grayalexanderi antiprotozoalactivityofpapuanewguineapropolisanditstriterpenes
AT fearnleyjames antiprotozoalactivityofpapuanewguineapropolisanditstriterpenes
AT dekoningharryp antiprotozoalactivityofpapuanewguineapropolisanditstriterpenes
AT watsondavidg antiprotozoalactivityofpapuanewguineapropolisanditstriterpenes