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Activity of the genus Zanthoxylum against diseases caused by protozoa: A systematic review

Neglected diseases (NDs) are treated with a less varied range of drugs, with high cost and toxicity, which makes the search for therapeutic alternatives important. In this context, plants, such as those from the genus Zanthoxylum, can be promising due to active substances in their composition. This...

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Autores principales: Correa-Barbosa, Juliana, Sodré, Daniele Ferreira, Nascimento, Pedro Henrique Costa, Dolabela, Maria Fâni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9868958/
https://www.ncbi.nlm.nih.gov/pubmed/36699053
http://dx.doi.org/10.3389/fphar.2022.873208
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author Correa-Barbosa, Juliana
Sodré, Daniele Ferreira
Nascimento, Pedro Henrique Costa
Dolabela, Maria Fâni
author_facet Correa-Barbosa, Juliana
Sodré, Daniele Ferreira
Nascimento, Pedro Henrique Costa
Dolabela, Maria Fâni
author_sort Correa-Barbosa, Juliana
collection PubMed
description Neglected diseases (NDs) are treated with a less varied range of drugs, with high cost and toxicity, which makes the search for therapeutic alternatives important. In this context, plants, such as those from the genus Zanthoxylum, can be promising due to active substances in their composition. This study evaluates the potential of species from this genus to treat NDs. Initially, a protocol was developed to carry out a systematic review approved by Prospero (CRD42020200438). The databases PubMed, BVS, Scopus, Science Direct, and Web of Science were used with the following keywords: “zanthoxylum,” “xanthoxylums,” “fagaras,” “leishmaniasis,” “chagas disease,” “malaria,” and “African trypanosomiasis.” Two independent evaluators analyzed the title and abstract of 166 articles, and 122 were excluded due to duplicity or for not meeting the inclusion criteria. From the 44 selected articles, results of in vitro/in vivo tests were extracted. In vitro studies showed that Z. rhoifolium, through the alkaloid nitidine, was active against Plasmodium (IC50 <1 μg/ml) and Leishmania (IC50 <8 μg/ml), and selective for both (>10 and >30, respectively). For Chagas disease, the promising species (IC50 <2 μg/ml) were Z. naranjillo and Z. minutiflorum, and for sleeping sickness, the species Z. zanthoxyloides (IC50 <4 μg/ml) stood out. In the in vivo analysis, the most promising species were Z. rhoifolium and Z. chiloperone. In summary, the species Z. rhoifolium, Z. naranjillo, Z. minutiflorum, Z. zanthoxyloides, and Z. chiloperone are promising sources of active molecules for the treatment of NDs.
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spelling pubmed-98689582023-01-24 Activity of the genus Zanthoxylum against diseases caused by protozoa: A systematic review Correa-Barbosa, Juliana Sodré, Daniele Ferreira Nascimento, Pedro Henrique Costa Dolabela, Maria Fâni Front Pharmacol Pharmacology Neglected diseases (NDs) are treated with a less varied range of drugs, with high cost and toxicity, which makes the search for therapeutic alternatives important. In this context, plants, such as those from the genus Zanthoxylum, can be promising due to active substances in their composition. This study evaluates the potential of species from this genus to treat NDs. Initially, a protocol was developed to carry out a systematic review approved by Prospero (CRD42020200438). The databases PubMed, BVS, Scopus, Science Direct, and Web of Science were used with the following keywords: “zanthoxylum,” “xanthoxylums,” “fagaras,” “leishmaniasis,” “chagas disease,” “malaria,” and “African trypanosomiasis.” Two independent evaluators analyzed the title and abstract of 166 articles, and 122 were excluded due to duplicity or for not meeting the inclusion criteria. From the 44 selected articles, results of in vitro/in vivo tests were extracted. In vitro studies showed that Z. rhoifolium, through the alkaloid nitidine, was active against Plasmodium (IC50 <1 μg/ml) and Leishmania (IC50 <8 μg/ml), and selective for both (>10 and >30, respectively). For Chagas disease, the promising species (IC50 <2 μg/ml) were Z. naranjillo and Z. minutiflorum, and for sleeping sickness, the species Z. zanthoxyloides (IC50 <4 μg/ml) stood out. In the in vivo analysis, the most promising species were Z. rhoifolium and Z. chiloperone. In summary, the species Z. rhoifolium, Z. naranjillo, Z. minutiflorum, Z. zanthoxyloides, and Z. chiloperone are promising sources of active molecules for the treatment of NDs. Frontiers Media S.A. 2023-01-09 /pmc/articles/PMC9868958/ /pubmed/36699053 http://dx.doi.org/10.3389/fphar.2022.873208 Text en Copyright © 2023 Correa-Barbosa, Sodré, Nascimento and Dolabela. https://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
Correa-Barbosa, Juliana
Sodré, Daniele Ferreira
Nascimento, Pedro Henrique Costa
Dolabela, Maria Fâni
Activity of the genus Zanthoxylum against diseases caused by protozoa: A systematic review
title Activity of the genus Zanthoxylum against diseases caused by protozoa: A systematic review
title_full Activity of the genus Zanthoxylum against diseases caused by protozoa: A systematic review
title_fullStr Activity of the genus Zanthoxylum against diseases caused by protozoa: A systematic review
title_full_unstemmed Activity of the genus Zanthoxylum against diseases caused by protozoa: A systematic review
title_short Activity of the genus Zanthoxylum against diseases caused by protozoa: A systematic review
title_sort activity of the genus zanthoxylum against diseases caused by protozoa: a systematic review
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9868958/
https://www.ncbi.nlm.nih.gov/pubmed/36699053
http://dx.doi.org/10.3389/fphar.2022.873208
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