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Antimalarial activity and toxicity evaluation of a quantified Nauclea pobeguinii extract

Identifieur interne : 001763 ( Main/Exploration ); précédent : 001762; suivant : 001764

Antimalarial activity and toxicity evaluation of a quantified Nauclea pobeguinii extract

Auteurs : Kahunu Mesia [République du Congo, Belgique] ; Richard K. Cimanga [République du Congo, Belgique] ; Liene Dhooghe [Belgique] ; Paul Cos [Belgique] ; Sandra Apers [Belgique] ; Jozef Totte [Belgique] ; Gaston L. Tona [République du Congo] ; Luc Pieters [Belgique] ; Arnold J. Vlietinck [Belgique] ; Louis Maes [Belgique]

Source :

RBID : Pascal:10-0417865

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English descriptors

Abstract

Aim of the study: To evaluate the in vitro and in vivo antiplasmodial activity and toxicity of the aqueous and 80% EtOH extract of the stem bark of Nauclea pobeguinii (Pob. Ex. Pell.) Petit (Rubiaceae), a plant used in traditional medicine in DR Congo against malaria. Materials and methods: The aqueous and 80% EtOH extract from N. pobeguinii stem bark, and its constituents (5S)-5-carboxystrictosidine, 19-O-methylangustoline, 3-O-β-fucosylquinovic acid, 3-ketoquinovic acid and strictosamide, were evaluated for their in vitro activity against Plasmodium falciparum (chloroquine-sensitive Ghana-strain). The 80% EtOH extract, containing 5.6% strictosamide, was evaluated in vivo in the 4-day P. berghei mouse model, and in the P. yoelii N67 model. Results: All compounds were inactive or only moderately active in vitro. The aqueous and 80% EtOH extract displayed moderate in vitro activity with IC50 values of 44 and 32 μg/mL, respectively, without apparent cytotoxicity on MRC-5 cells (CC50>64 μg/mL). Daily oral dosing of the 80% EtOH extract, at 300 mg/kg, resulted in 86% reduction of parasitaemia in the 4-day P. berghei mouse model, and 75% reduction in the P. yoelii N67 model. Prolonging oral dosing to 2 x 5 days, with an interval of 2 days, and oral administration of the 80% EtOH extract at 300 mg/kg induced 92% reduction of parasitaemia, and a mean survival time of 17 days. Strictosamide, the putative active constituent, may be metabolically activated in the gastrointestinal tract after oral administration. Levels of creatinin, urea, ALAT and ASAT remained unchanged after treatment. No acute toxicity was observed in mice after a single 2 g/kg oral dose, nor after 4 weekly doses. No significant macroscopic or microscopic lesions were observed in heart, lung, spleen, kidney, liver, large intestine and brain. Conclusions: These results can partly support and justify the use of N. pobeguinii in traditional medicine in the DR Congo for the treatment of uncomplicated malaria.


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<s1>Laboratory of Pharmacognosy and Pharmaceutical Analysis, Department of Pharmaceutical Sciences, University of Antwerp, Universiteitsplein 1</s1>
<s2>2610 Antwerp</s2>
<s3>BEL</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>8 aut.</sZ>
<sZ>9 aut.</sZ>
</inist:fA14>
<country>Belgique</country>
<wicri:noRegion>2610 Antwerp</wicri:noRegion>
<orgName type="university">Université d'Anvers</orgName>
<placeName>
<settlement type="city">Anvers</settlement>
<region>Région flamande</region>
<region type="district" nuts="2">Province d'Anvers</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Maes, Louis" sort="Maes, Louis" uniqKey="Maes L" first="Louis" last="Maes">Louis Maes</name>
<affiliation wicri:level="4">
<inist:fA14 i1="03">
<s1>Laboratory of Microbiology and Parasitology (LMPH), Faculty of Pharmaceutical, Biomedical and Veterinary Sciences, University of Antwerp, Groenenborgerlaan 171</s1>
<s2>2020 Antwerpen</s2>
<s3>BEL</s3>
<sZ>4 aut.</sZ>
<sZ>10 aut.</sZ>
</inist:fA14>
<country>Belgique</country>
<placeName>
<region type="province" nuts="2">Province d'Anvers</region>
<settlement type="city">Anvers</settlement>
</placeName>
<orgName type="university">Université d'Anvers</orgName>
</affiliation>
</author>
</analytic>
<series>
<title level="j" type="main">Journal of ethnopharmacology</title>
<title level="j" type="abbreviated">J. ethnopharmacol.</title>
<idno type="ISSN">0378-8741</idno>
<imprint>
<date when="2010">2010</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt>
<title level="j" type="main">Journal of ethnopharmacology</title>
<title level="j" type="abbreviated">J. ethnopharmacol.</title>
<idno type="ISSN">0378-8741</idno>
</seriesStmt>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Antimalarial</term>
<term>Evaluation</term>
<term>Extract</term>
<term>Malaria</term>
<term>Medicinal plant</term>
<term>Parasiticide</term>
<term>Pharmacognosy</term>
<term>Plant origin</term>
<term>Rubiaceae</term>
<term>Toxicity</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Antipaludique</term>
<term>Antiparasitaire</term>
<term>Toxicité</term>
<term>Evaluation</term>
<term>Extrait</term>
<term>Rubiaceae</term>
<term>Paludisme</term>
<term>Pharmacognosie</term>
<term>Plante médicinale</term>
<term>Origine végétale</term>
<term>Nauclea</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr">
<term>Plante médicinale</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">Aim of the study: To evaluate the in vitro and in vivo antiplasmodial activity and toxicity of the aqueous and 80% EtOH extract of the stem bark of Nauclea pobeguinii (Pob. Ex. Pell.) Petit (Rubiaceae), a plant used in traditional medicine in DR Congo against malaria. Materials and methods: The aqueous and 80% EtOH extract from N. pobeguinii stem bark, and its constituents (5S)-5-carboxystrictosidine, 19-O-methylangustoline, 3-O-β-fucosylquinovic acid, 3-ketoquinovic acid and strictosamide, were evaluated for their in vitro activity against Plasmodium falciparum (chloroquine-sensitive Ghana-strain). The 80% EtOH extract, containing 5.6% strictosamide, was evaluated in vivo in the 4-day P. berghei mouse model, and in the P. yoelii N67 model. Results: All compounds were inactive or only moderately active in vitro. The aqueous and 80% EtOH extract displayed moderate in vitro activity with IC
<sub>50</sub>
values of 44 and 32 μg/mL, respectively, without apparent cytotoxicity on MRC-5 cells (CC50>64 μg/mL). Daily oral dosing of the 80% EtOH extract, at 300 mg/kg, resulted in 86% reduction of parasitaemia in the 4-day P. berghei mouse model, and 75% reduction in the P. yoelii N67 model. Prolonging oral dosing to 2 x 5 days, with an interval of 2 days, and oral administration of the 80% EtOH extract at 300 mg/kg induced 92% reduction of parasitaemia, and a mean survival time of 17 days. Strictosamide, the putative active constituent, may be metabolically activated in the gastrointestinal tract after oral administration. Levels of creatinin, urea, ALAT and ASAT remained unchanged after treatment. No acute toxicity was observed in mice after a single 2 g/kg oral dose, nor after 4 weekly doses. No significant macroscopic or microscopic lesions were observed in heart, lung, spleen, kidney, liver, large intestine and brain. Conclusions: These results can partly support and justify the use of N. pobeguinii in traditional medicine in the DR Congo for the treatment of uncomplicated malaria.</div>
</front>
</TEI>
<affiliations>
<list>
<country>
<li>Belgique</li>
<li>République du Congo</li>
</country>
<region>
<li>Province d'Anvers</li>
<li>Région flamande</li>
</region>
<settlement>
<li>Anvers</li>
</settlement>
<orgName>
<li>Université d'Anvers</li>
</orgName>
</list>
<tree>
<country name="République du Congo">
<noRegion>
<name sortKey="Mesia, Kahunu" sort="Mesia, Kahunu" uniqKey="Mesia K" first="Kahunu" last="Mesia">Kahunu Mesia</name>
</noRegion>
<name sortKey="Cimanga, Richard K" sort="Cimanga, Richard K" uniqKey="Cimanga R" first="Richard K." last="Cimanga">Richard K. Cimanga</name>
<name sortKey="Tona, Gaston L" sort="Tona, Gaston L" uniqKey="Tona G" first="Gaston L." last="Tona">Gaston L. Tona</name>
</country>
<country name="Belgique">
<region name="Région flamande">
<name sortKey="Mesia, Kahunu" sort="Mesia, Kahunu" uniqKey="Mesia K" first="Kahunu" last="Mesia">Kahunu Mesia</name>
</region>
<name sortKey="Apers, Sandra" sort="Apers, Sandra" uniqKey="Apers S" first="Sandra" last="Apers">Sandra Apers</name>
<name sortKey="Cimanga, Richard K" sort="Cimanga, Richard K" uniqKey="Cimanga R" first="Richard K." last="Cimanga">Richard K. Cimanga</name>
<name sortKey="Cos, Paul" sort="Cos, Paul" uniqKey="Cos P" first="Paul" last="Cos">Paul Cos</name>
<name sortKey="Dhooghe, Liene" sort="Dhooghe, Liene" uniqKey="Dhooghe L" first="Liene" last="Dhooghe">Liene Dhooghe</name>
<name sortKey="Maes, Louis" sort="Maes, Louis" uniqKey="Maes L" first="Louis" last="Maes">Louis Maes</name>
<name sortKey="Pieters, Luc" sort="Pieters, Luc" uniqKey="Pieters L" first="Luc" last="Pieters">Luc Pieters</name>
<name sortKey="Totte, Jozef" sort="Totte, Jozef" uniqKey="Totte J" first="Jozef" last="Totte">Jozef Totte</name>
<name sortKey="Vlietinck, Arnold J" sort="Vlietinck, Arnold J" uniqKey="Vlietinck A" first="Arnold J." last="Vlietinck">Arnold J. Vlietinck</name>
</country>
</tree>
</affiliations>
</record>

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