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In vivo validation of anti-malarial activity of crude extracts of Terminalia macroptera, a Malian medicinal plant

BACKGROUND: Plasmodium falciparum malaria is still one of the most deadly pathology worldwide. Efficient treatment is jeopardized by parasite resistance to artemisinin and its derivatives, and by poor access to treatment in endemic regions. Anti-malarial traditional remedies still offer new tracks f...

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Autores principales: Haidara, Mahamane, Haddad, Mohamed, Denou, Adama, Marti, Guillaume, Bourgeade-Delmas, Sandra, Sanogo, Rokia, Bourdy, Geneviève, Aubouy, Agnès
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5800286/
https://www.ncbi.nlm.nih.gov/pubmed/29402267
http://dx.doi.org/10.1186/s12936-018-2223-7
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author Haidara, Mahamane
Haddad, Mohamed
Denou, Adama
Marti, Guillaume
Bourgeade-Delmas, Sandra
Sanogo, Rokia
Bourdy, Geneviève
Aubouy, Agnès
author_facet Haidara, Mahamane
Haddad, Mohamed
Denou, Adama
Marti, Guillaume
Bourgeade-Delmas, Sandra
Sanogo, Rokia
Bourdy, Geneviève
Aubouy, Agnès
author_sort Haidara, Mahamane
collection PubMed
description BACKGROUND: Plasmodium falciparum malaria is still one of the most deadly pathology worldwide. Efficient treatment is jeopardized by parasite resistance to artemisinin and its derivatives, and by poor access to treatment in endemic regions. Anti-malarial traditional remedies still offer new tracks for identifying promising antiplasmodial molecules, and a way to ensure that all people have access to care. The present study aims to validate the traditional use of Terminalia macroptera, a Malian plant used in traditional medicine. METHODS: Terminalia macroptera was collected in Mali. Leaves (TML) and roots ethanolic extracts (TMR) were prepared and tested at 2000 mg/kg for in vivo acute toxicity in Albino Swiss mice. Antiplasmodial activity of the extracts was assessed against a chloroquine resistant strain P. falciparum (FcB1) in vitro. In vivo, anti-malarial efficacy was assessed by a 4-day suppressive test at 100 mg/kg in two malaria murine models of uncomplicated malaria (Plasmodium chabaudi chabaudi infection) and cerebral malaria (Plasmodium berghei strain ANKA infection). Constituents of TMR were characterized by ultra-high-performance liquid chromatography coupled to high resolution mass spectrometry. Top ranked compounds were putatively identified using plant databases and in silico fragmentation pattern. RESULTS: Lethal dose of TML and TMR were greater than 2000 mg/kg in Albino Swiss mice. According to the OECD’s Globally Harmonized System of Classification, both extracts are non-toxic orally. Antiplasmodial activity of T. macroptera extracts was confirmed in vitro against P. falciparum FcB1 strain with IC50 values of 1.2 and 1.6 µg/mL for TML and TMR, respectively. In vivo, oral administration of TML and TMR induced significant reduction of parasitaemia (37.2 and 46.4% respectively) in P. chabaudi chabaudi infected mice at the 7th day of infection compared to untreated mice. In the cerebral malaria experimental model, mice treated with TMR and TML presented respectively 50 and 66.7% survival rates at day 9 post-infection when all untreated mice died. Eleven major compounds were found in TMR. Among them, several molecules already known could be responsible for the antiplasmodial activity of the roots extract of T. macroptera. CONCLUSIONS: This study confirms both safety and anti-malarial activity of T. macroptera, thus validating its traditional use.
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spelling pubmed-58002862018-02-13 In vivo validation of anti-malarial activity of crude extracts of Terminalia macroptera, a Malian medicinal plant Haidara, Mahamane Haddad, Mohamed Denou, Adama Marti, Guillaume Bourgeade-Delmas, Sandra Sanogo, Rokia Bourdy, Geneviève Aubouy, Agnès Malar J Research BACKGROUND: Plasmodium falciparum malaria is still one of the most deadly pathology worldwide. Efficient treatment is jeopardized by parasite resistance to artemisinin and its derivatives, and by poor access to treatment in endemic regions. Anti-malarial traditional remedies still offer new tracks for identifying promising antiplasmodial molecules, and a way to ensure that all people have access to care. The present study aims to validate the traditional use of Terminalia macroptera, a Malian plant used in traditional medicine. METHODS: Terminalia macroptera was collected in Mali. Leaves (TML) and roots ethanolic extracts (TMR) were prepared and tested at 2000 mg/kg for in vivo acute toxicity in Albino Swiss mice. Antiplasmodial activity of the extracts was assessed against a chloroquine resistant strain P. falciparum (FcB1) in vitro. In vivo, anti-malarial efficacy was assessed by a 4-day suppressive test at 100 mg/kg in two malaria murine models of uncomplicated malaria (Plasmodium chabaudi chabaudi infection) and cerebral malaria (Plasmodium berghei strain ANKA infection). Constituents of TMR were characterized by ultra-high-performance liquid chromatography coupled to high resolution mass spectrometry. Top ranked compounds were putatively identified using plant databases and in silico fragmentation pattern. RESULTS: Lethal dose of TML and TMR were greater than 2000 mg/kg in Albino Swiss mice. According to the OECD’s Globally Harmonized System of Classification, both extracts are non-toxic orally. Antiplasmodial activity of T. macroptera extracts was confirmed in vitro against P. falciparum FcB1 strain with IC50 values of 1.2 and 1.6 µg/mL for TML and TMR, respectively. In vivo, oral administration of TML and TMR induced significant reduction of parasitaemia (37.2 and 46.4% respectively) in P. chabaudi chabaudi infected mice at the 7th day of infection compared to untreated mice. In the cerebral malaria experimental model, mice treated with TMR and TML presented respectively 50 and 66.7% survival rates at day 9 post-infection when all untreated mice died. Eleven major compounds were found in TMR. Among them, several molecules already known could be responsible for the antiplasmodial activity of the roots extract of T. macroptera. CONCLUSIONS: This study confirms both safety and anti-malarial activity of T. macroptera, thus validating its traditional use. BioMed Central 2018-02-05 /pmc/articles/PMC5800286/ /pubmed/29402267 http://dx.doi.org/10.1186/s12936-018-2223-7 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Haidara, Mahamane
Haddad, Mohamed
Denou, Adama
Marti, Guillaume
Bourgeade-Delmas, Sandra
Sanogo, Rokia
Bourdy, Geneviève
Aubouy, Agnès
In vivo validation of anti-malarial activity of crude extracts of Terminalia macroptera, a Malian medicinal plant
title In vivo validation of anti-malarial activity of crude extracts of Terminalia macroptera, a Malian medicinal plant
title_full In vivo validation of anti-malarial activity of crude extracts of Terminalia macroptera, a Malian medicinal plant
title_fullStr In vivo validation of anti-malarial activity of crude extracts of Terminalia macroptera, a Malian medicinal plant
title_full_unstemmed In vivo validation of anti-malarial activity of crude extracts of Terminalia macroptera, a Malian medicinal plant
title_short In vivo validation of anti-malarial activity of crude extracts of Terminalia macroptera, a Malian medicinal plant
title_sort in vivo validation of anti-malarial activity of crude extracts of terminalia macroptera, a malian medicinal plant
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5800286/
https://www.ncbi.nlm.nih.gov/pubmed/29402267
http://dx.doi.org/10.1186/s12936-018-2223-7
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