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HPLC-Based Activity Profiling for Antiprotozoal Compounds in Croton gratissimus and Cuscuta hyalina
In a screening of Sudanese medicinal plants for antiprotozoal activity, the chloroform fractions obtained by liquid-liquid partitioning from ethanolic extracts of fruits of Croton gratissimus var. gratissimus and stems of Cuscuta hyalina Roth ex Schult. exhibited in vitro activity against axenically...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7456963/ https://www.ncbi.nlm.nih.gov/pubmed/32922290 http://dx.doi.org/10.3389/fphar.2020.01246 |
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author | Mahmoud, Abdelhalim Babiker Danton, Ombeline Kaiser, Marcel Khalid, Sami Hamburger, Matthias Mäser, Pascal |
author_facet | Mahmoud, Abdelhalim Babiker Danton, Ombeline Kaiser, Marcel Khalid, Sami Hamburger, Matthias Mäser, Pascal |
author_sort | Mahmoud, Abdelhalim Babiker |
collection | PubMed |
description | In a screening of Sudanese medicinal plants for antiprotozoal activity, the chloroform fractions obtained by liquid-liquid partitioning from ethanolic extracts of fruits of Croton gratissimus var. gratissimus and stems of Cuscuta hyalina Roth ex Schult. exhibited in vitro activity against axenically grown Leishmania donovani amastigotes. This antileishmanial activity was localized by HPLC-based activity profiling. Targeted preparative isolation afforded flavonoids 1–6, 3-methoxy-4-hydroxybenzoic acid (7), and benzyltetrahydroisoquinoline alkaloids laudanine (8) and laudanosine (9) from C. gratissimus, and pinoresinol (10), isorhamnetin (11), (-)-pseudosemiglabrin (12), and kaempferol (13) from C. hyalina. The antiprotozoal activity of 1–13 against L. donovani (axenic and intracellular amastigotes), Trypanosoma brucei rhodesiense (bloodstream forms), and Plasmodium falciparum (erythrocytic stages), and the cytotoxicity in L6 murine myoblast cells were determined in vitro. Quercetin-3,7-dimethylether (6) showed the highest activity against axenic L. donovani (IC(50,) 4.5 µM; selectivity index [SI], 12.3), P. falciparum (IC(50,) 7.3 µM; SI, 7.6), and T. b. rhodesiense (IC(50), 2.4 µM; SI, 23.2). The congener ayanin (2) exhibited moderate antileishmanial (IC(50), 8.2 µM; SI, 12.2), antiplasmodial (IC(50), 7.8 µM; SI, 12.9), and antitrypanosomal activity (IC(50), 11.2 µM; SI, 8.9). None of the compounds showed notable activity against the intramacrophage form of L. donovani. |
format | Online Article Text |
id | pubmed-7456963 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74569632020-09-11 HPLC-Based Activity Profiling for Antiprotozoal Compounds in Croton gratissimus and Cuscuta hyalina Mahmoud, Abdelhalim Babiker Danton, Ombeline Kaiser, Marcel Khalid, Sami Hamburger, Matthias Mäser, Pascal Front Pharmacol Pharmacology In a screening of Sudanese medicinal plants for antiprotozoal activity, the chloroform fractions obtained by liquid-liquid partitioning from ethanolic extracts of fruits of Croton gratissimus var. gratissimus and stems of Cuscuta hyalina Roth ex Schult. exhibited in vitro activity against axenically grown Leishmania donovani amastigotes. This antileishmanial activity was localized by HPLC-based activity profiling. Targeted preparative isolation afforded flavonoids 1–6, 3-methoxy-4-hydroxybenzoic acid (7), and benzyltetrahydroisoquinoline alkaloids laudanine (8) and laudanosine (9) from C. gratissimus, and pinoresinol (10), isorhamnetin (11), (-)-pseudosemiglabrin (12), and kaempferol (13) from C. hyalina. The antiprotozoal activity of 1–13 against L. donovani (axenic and intracellular amastigotes), Trypanosoma brucei rhodesiense (bloodstream forms), and Plasmodium falciparum (erythrocytic stages), and the cytotoxicity in L6 murine myoblast cells were determined in vitro. Quercetin-3,7-dimethylether (6) showed the highest activity against axenic L. donovani (IC(50,) 4.5 µM; selectivity index [SI], 12.3), P. falciparum (IC(50,) 7.3 µM; SI, 7.6), and T. b. rhodesiense (IC(50), 2.4 µM; SI, 23.2). The congener ayanin (2) exhibited moderate antileishmanial (IC(50), 8.2 µM; SI, 12.2), antiplasmodial (IC(50), 7.8 µM; SI, 12.9), and antitrypanosomal activity (IC(50), 11.2 µM; SI, 8.9). None of the compounds showed notable activity against the intramacrophage form of L. donovani. Frontiers Media S.A. 2020-08-14 /pmc/articles/PMC7456963/ /pubmed/32922290 http://dx.doi.org/10.3389/fphar.2020.01246 Text en Copyright © 2020 Mahmoud, Danton, Kaiser, Khalid, Hamburger and Mäser http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Mahmoud, Abdelhalim Babiker Danton, Ombeline Kaiser, Marcel Khalid, Sami Hamburger, Matthias Mäser, Pascal HPLC-Based Activity Profiling for Antiprotozoal Compounds in Croton gratissimus and Cuscuta hyalina |
title | HPLC-Based Activity Profiling for Antiprotozoal Compounds in Croton gratissimus and Cuscuta hyalina
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title_full | HPLC-Based Activity Profiling for Antiprotozoal Compounds in Croton gratissimus and Cuscuta hyalina
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title_fullStr | HPLC-Based Activity Profiling for Antiprotozoal Compounds in Croton gratissimus and Cuscuta hyalina
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title_full_unstemmed | HPLC-Based Activity Profiling for Antiprotozoal Compounds in Croton gratissimus and Cuscuta hyalina
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title_short | HPLC-Based Activity Profiling for Antiprotozoal Compounds in Croton gratissimus and Cuscuta hyalina
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title_sort | hplc-based activity profiling for antiprotozoal compounds in croton gratissimus and cuscuta hyalina |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7456963/ https://www.ncbi.nlm.nih.gov/pubmed/32922290 http://dx.doi.org/10.3389/fphar.2020.01246 |
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