Serveur d'exploration Chloroquine

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

In vitro and in vivo antimalarial and cytotoxic activity of five plants used in congolese traditional medicine

Identifieur interne : 001761 ( Main/Exploration ); précédent : 001760; suivant : 001762

In vitro and in vivo antimalarial and cytotoxic activity of five plants used in congolese traditional medicine

Auteurs : M. Lusakibanza [République du Congo] ; G. Mesia [République du Congo] ; G. Tona [République du Congo] ; S. Karemere [République du Congo] ; A. Lukuka [République du Congo] ; M. Tits [Belgique] ; L. Angenot [Belgique] ; M. Frederich [Belgique]

Source :

RBID : Pascal:10-0330894

Descripteurs français

English descriptors

Abstract

Aim of the study: The in vitro antiplasmodial activity and cytotoxicity of methanolic and dichloromethane extracts from five Congolese plants were evaluated. The plants were selected following an ethnobotanical survey conducted in D.R. Congo and focusing on plants used traditionally to treat malaria. The in vivo antimalarial activity of aqueous and methanolic extracts active in vitro was also determined in mice infected by Plasmodium berghei berghei. Materials and methods: The growth inhibition of Plasmodiumfalciparum strains was evaluated using the measurement of lactate dehydrogenase activity. The extracts (aqueous, CH3OH, EtOH and CH2Cl2) were prepared by maceration and tested in vitro against the 3D7 (chloroquine sensitive) and W2 (chloroquine resistant) strains of Plasmodiumfalciparum and against the human normal fetal lung fibroblasts WI-38 to determine the selectivity index. Some extracts were also used at the dose of 300 mg/kg to evaluate their activity in mice infected since 4 days by Plasmodium berghei. Results: Two plants presented a very high activity (IC50 < 3 μg/ml). These plants were Strychnos icaja roots bark (MeOH and CH2Cl2) and Physalis angulata leaves (MeOH and CH2Cl2). One plant (Anisopappus chinensis whole plant, MeOH and CH2Cl2) presented a high activity (IC50 < 15 μg/ml). The extracts of Anisopappus chinensis and Physalis angulata showed also a good inhibition of parasitemia in vivo. Flavonoids, phenolic acids and terpenes were identified in these plants by a general phytochemical screening method. Conclusion: Three plants showed a very interesting antiplasmodial activity (Anisopappus chinensis, Physalis angulata and Strychnos icaja) and one of them showed a good selectivity index (>10, Anisopappus chinensis). Anisopappus chinensis and Physalis angulata were also active in vivo.


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

<record>
<TEI>
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en" level="a">In vitro and in vivo antimalarial and cytotoxic activity of five plants used in congolese traditional medicine</title>
<author>
<name sortKey="Lusakibanza, M" sort="Lusakibanza, M" uniqKey="Lusakibanza M" first="M." last="Lusakibanza">M. Lusakibanza</name>
<affiliation wicri:level="1">
<inist:fA14 i1="01">
<s1>University of Kinshasa, Faculty of Pharmaceuticals Sciences, Laboratory of Pharmacology, B.P. 212</s1>
<s2>Kinshasa XI</s2>
<s3>COG</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</inist:fA14>
<country>République du Congo</country>
<wicri:noRegion>Kinshasa XI</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Mesia, G" sort="Mesia, G" uniqKey="Mesia G" first="G." last="Mesia">G. Mesia</name>
<affiliation wicri:level="1">
<inist:fA14 i1="01">
<s1>University of Kinshasa, Faculty of Pharmaceuticals Sciences, Laboratory of Pharmacology, B.P. 212</s1>
<s2>Kinshasa XI</s2>
<s3>COG</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</inist:fA14>
<country>République du Congo</country>
<wicri:noRegion>Kinshasa XI</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Tona, G" sort="Tona, G" uniqKey="Tona G" first="G." last="Tona">G. Tona</name>
<affiliation wicri:level="1">
<inist:fA14 i1="01">
<s1>University of Kinshasa, Faculty of Pharmaceuticals Sciences, Laboratory of Pharmacology, B.P. 212</s1>
<s2>Kinshasa XI</s2>
<s3>COG</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</inist:fA14>
<country>République du Congo</country>
<wicri:noRegion>Kinshasa XI</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Karemere, S" sort="Karemere, S" uniqKey="Karemere S" first="S." last="Karemere">S. Karemere</name>
<affiliation wicri:level="1">
<inist:fA14 i1="02">
<s1>Institut National de Recherches Biomédicales, Avenue de la démocratie 7, B.P. 119</s1>
<s2>Kinshasa</s2>
<s3>COG</s3>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
<country>République du Congo</country>
<wicri:noRegion>Kinshasa</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Lukuka, A" sort="Lukuka, A" uniqKey="Lukuka A" first="A." last="Lukuka">A. Lukuka</name>
<affiliation wicri:level="1">
<inist:fA14 i1="02">
<s1>Institut National de Recherches Biomédicales, Avenue de la démocratie 7, B.P. 119</s1>
<s2>Kinshasa</s2>
<s3>COG</s3>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
<country>République du Congo</country>
<wicri:noRegion>Kinshasa</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Tits, M" sort="Tits, M" uniqKey="Tits M" first="M." last="Tits">M. Tits</name>
<affiliation wicri:level="4">
<inist:fA14 i1="03">
<s1>Université de Liège, CIRM, Laboratoire de Pharmacognosie, Av de l'Hôpital 1, B36</s1>
<s2>4000 Liège</s2>
<s3>BEL</s3>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>8 aut.</sZ>
</inist:fA14>
<country>Belgique</country>
<placeName>
<region type="province" nuts="2">Province de Liège</region>
<settlement type="city">Liège</settlement>
</placeName>
<orgName type="university">Université de Liège</orgName>
</affiliation>
</author>
<author>
<name sortKey="Angenot, L" sort="Angenot, L" uniqKey="Angenot L" first="L." last="Angenot">L. Angenot</name>
<affiliation wicri:level="4">
<inist:fA14 i1="03">
<s1>Université de Liège, CIRM, Laboratoire de Pharmacognosie, Av de l'Hôpital 1, B36</s1>
<s2>4000 Liège</s2>
<s3>BEL</s3>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>8 aut.</sZ>
</inist:fA14>
<country>Belgique</country>
<placeName>
<region type="province" nuts="2">Province de Liège</region>
<settlement type="city">Liège</settlement>
</placeName>
<orgName type="university">Université de Liège</orgName>
</affiliation>
</author>
<author>
<name sortKey="Frederich, M" sort="Frederich, M" uniqKey="Frederich M" first="M." last="Frederich">M. Frederich</name>
<affiliation wicri:level="4">
<inist:fA14 i1="03">
<s1>Université de Liège, CIRM, Laboratoire de Pharmacognosie, Av de l'Hôpital 1, B36</s1>
<s2>4000 Liège</s2>
<s3>BEL</s3>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>8 aut.</sZ>
</inist:fA14>
<country>Belgique</country>
<placeName>
<region type="province" nuts="2">Province de Liège</region>
<settlement type="city">Liège</settlement>
</placeName>
<orgName type="university">Université de Liège</orgName>
</affiliation>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">INIST</idno>
<idno type="inist">10-0330894</idno>
<date when="2010">2010</date>
<idno type="stanalyst">PASCAL 10-0330894 INIST</idno>
<idno type="RBID">Pascal:10-0330894</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">000019</idno>
<idno type="wicri:Area/PascalFrancis/Curation">000047</idno>
<idno type="wicri:Area/PascalFrancis/Checkpoint">000018</idno>
<idno type="wicri:explorRef" wicri:stream="PascalFrancis" wicri:step="Checkpoint">000018</idno>
<idno type="wicri:doubleKey">0378-8741:2010:Lusakibanza M:in:vitro:and</idno>
<idno type="wicri:Area/Main/Merge">001764</idno>
<idno type="wicri:Area/Main/Curation">001761</idno>
<idno type="wicri:Area/Main/Exploration">001761</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title xml:lang="en" level="a">In vitro and in vivo antimalarial and cytotoxic activity of five plants used in congolese traditional medicine</title>
<author>
<name sortKey="Lusakibanza, M" sort="Lusakibanza, M" uniqKey="Lusakibanza M" first="M." last="Lusakibanza">M. Lusakibanza</name>
<affiliation wicri:level="1">
<inist:fA14 i1="01">
<s1>University of Kinshasa, Faculty of Pharmaceuticals Sciences, Laboratory of Pharmacology, B.P. 212</s1>
<s2>Kinshasa XI</s2>
<s3>COG</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</inist:fA14>
<country>République du Congo</country>
<wicri:noRegion>Kinshasa XI</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Mesia, G" sort="Mesia, G" uniqKey="Mesia G" first="G." last="Mesia">G. Mesia</name>
<affiliation wicri:level="1">
<inist:fA14 i1="01">
<s1>University of Kinshasa, Faculty of Pharmaceuticals Sciences, Laboratory of Pharmacology, B.P. 212</s1>
<s2>Kinshasa XI</s2>
<s3>COG</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</inist:fA14>
<country>République du Congo</country>
<wicri:noRegion>Kinshasa XI</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Tona, G" sort="Tona, G" uniqKey="Tona G" first="G." last="Tona">G. Tona</name>
<affiliation wicri:level="1">
<inist:fA14 i1="01">
<s1>University of Kinshasa, Faculty of Pharmaceuticals Sciences, Laboratory of Pharmacology, B.P. 212</s1>
<s2>Kinshasa XI</s2>
<s3>COG</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</inist:fA14>
<country>République du Congo</country>
<wicri:noRegion>Kinshasa XI</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Karemere, S" sort="Karemere, S" uniqKey="Karemere S" first="S." last="Karemere">S. Karemere</name>
<affiliation wicri:level="1">
<inist:fA14 i1="02">
<s1>Institut National de Recherches Biomédicales, Avenue de la démocratie 7, B.P. 119</s1>
<s2>Kinshasa</s2>
<s3>COG</s3>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
<country>République du Congo</country>
<wicri:noRegion>Kinshasa</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Lukuka, A" sort="Lukuka, A" uniqKey="Lukuka A" first="A." last="Lukuka">A. Lukuka</name>
<affiliation wicri:level="1">
<inist:fA14 i1="02">
<s1>Institut National de Recherches Biomédicales, Avenue de la démocratie 7, B.P. 119</s1>
<s2>Kinshasa</s2>
<s3>COG</s3>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
<country>République du Congo</country>
<wicri:noRegion>Kinshasa</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Tits, M" sort="Tits, M" uniqKey="Tits M" first="M." last="Tits">M. Tits</name>
<affiliation wicri:level="4">
<inist:fA14 i1="03">
<s1>Université de Liège, CIRM, Laboratoire de Pharmacognosie, Av de l'Hôpital 1, B36</s1>
<s2>4000 Liège</s2>
<s3>BEL</s3>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>8 aut.</sZ>
</inist:fA14>
<country>Belgique</country>
<placeName>
<region type="province" nuts="2">Province de Liège</region>
<settlement type="city">Liège</settlement>
</placeName>
<orgName type="university">Université de Liège</orgName>
</affiliation>
</author>
<author>
<name sortKey="Angenot, L" sort="Angenot, L" uniqKey="Angenot L" first="L." last="Angenot">L. Angenot</name>
<affiliation wicri:level="4">
<inist:fA14 i1="03">
<s1>Université de Liège, CIRM, Laboratoire de Pharmacognosie, Av de l'Hôpital 1, B36</s1>
<s2>4000 Liège</s2>
<s3>BEL</s3>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>8 aut.</sZ>
</inist:fA14>
<country>Belgique</country>
<placeName>
<region type="province" nuts="2">Province de Liège</region>
<settlement type="city">Liège</settlement>
</placeName>
<orgName type="university">Université de Liège</orgName>
</affiliation>
</author>
<author>
<name sortKey="Frederich, M" sort="Frederich, M" uniqKey="Frederich M" first="M." last="Frederich">M. Frederich</name>
<affiliation wicri:level="4">
<inist:fA14 i1="03">
<s1>Université de Liège, CIRM, Laboratoire de Pharmacognosie, Av de l'Hôpital 1, B36</s1>
<s2>4000 Liège</s2>
<s3>BEL</s3>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>8 aut.</sZ>
</inist:fA14>
<country>Belgique</country>
<placeName>
<region type="province" nuts="2">Province de Liège</region>
<settlement type="city">Liège</settlement>
</placeName>
<orgName type="university">Université de Liège</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>Cytotoxicity</term>
<term>Fibroblast</term>
<term>Folk medicine</term>
<term>Human</term>
<term>In vitro</term>
<term>Loganiaceae</term>
<term>Medicinal plant</term>
<term>Meliaceae</term>
<term>Parasiticide</term>
<term>Pesticide crop</term>
<term>Pharmacognosy</term>
<term>Plant origin</term>
<term>Solanaceae</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>In vitro</term>
<term>Antipaludique</term>
<term>Antiparasitaire</term>
<term>Cytotoxicité</term>
<term>Plante médicinale</term>
<term>Médecine traditionnelle</term>
<term>Homme</term>
<term>Fibroblaste</term>
<term>Pharmacognosie</term>
<term>Origine végétale</term>
<term>Meliaceae</term>
<term>Solanaceae</term>
<term>Plante pesticide</term>
<term>Loganiaceae</term>
<term>Entandrophragma</term>
<term>Melia azedarach</term>
<term>Physalis angulata</term>
<term>Strychnos</term>
<term>Plante pharmaceutique</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr">
<term>Plante médicinale</term>
<term>Homme</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">Aim of the study: The in vitro antiplasmodial activity and cytotoxicity of methanolic and dichloromethane extracts from five Congolese plants were evaluated. The plants were selected following an ethnobotanical survey conducted in D.R. Congo and focusing on plants used traditionally to treat malaria. The in vivo antimalarial activity of aqueous and methanolic extracts active in vitro was also determined in mice infected by Plasmodium berghei berghei. Materials and methods: The growth inhibition of Plasmodiumfalciparum strains was evaluated using the measurement of lactate dehydrogenase activity. The extracts (aqueous, CH
<sub>3</sub>
OH, EtOH and CH
<sub>2</sub>
Cl
<sub>2</sub>
) were prepared by maceration and tested in vitro against the 3D7 (chloroquine sensitive) and W2 (chloroquine resistant) strains of Plasmodiumfalciparum and against the human normal fetal lung fibroblasts WI-38 to determine the selectivity index. Some extracts were also used at the dose of 300 mg/kg to evaluate their activity in mice infected since 4 days by Plasmodium berghei. Results: Two plants presented a very high activity (IC
<sub>50</sub>
< 3 μg/ml). These plants were Strychnos icaja roots bark (MeOH and CH
<sub>2</sub>
Cl
<sub>2</sub>
) and Physalis angulata leaves (MeOH and CH
<sub>2</sub>
Cl
<sub>2</sub>
). One plant (Anisopappus chinensis whole plant, MeOH and CH
<sub>2</sub>
Cl
<sub>2</sub>
) presented a high activity (IC50 < 15 μg/ml). The extracts of Anisopappus chinensis and Physalis angulata showed also a good inhibition of parasitemia in vivo. Flavonoids, phenolic acids and terpenes were identified in these plants by a general phytochemical screening method. Conclusion: Three plants showed a very interesting antiplasmodial activity (Anisopappus chinensis, Physalis angulata and Strychnos icaja) and one of them showed a good selectivity index (>10, Anisopappus chinensis). Anisopappus chinensis and Physalis angulata were also active in vivo.</div>
</front>
</TEI>
<affiliations>
<list>
<country>
<li>Belgique</li>
<li>République du Congo</li>
</country>
<region>
<li>Province de Liège</li>
</region>
<settlement>
<li>Liège</li>
</settlement>
<orgName>
<li>Université de Liège</li>
</orgName>
</list>
<tree>
<country name="République du Congo">
<noRegion>
<name sortKey="Lusakibanza, M" sort="Lusakibanza, M" uniqKey="Lusakibanza M" first="M." last="Lusakibanza">M. Lusakibanza</name>
</noRegion>
<name sortKey="Karemere, S" sort="Karemere, S" uniqKey="Karemere S" first="S." last="Karemere">S. Karemere</name>
<name sortKey="Lukuka, A" sort="Lukuka, A" uniqKey="Lukuka A" first="A." last="Lukuka">A. Lukuka</name>
<name sortKey="Mesia, G" sort="Mesia, G" uniqKey="Mesia G" first="G." last="Mesia">G. Mesia</name>
<name sortKey="Tona, G" sort="Tona, G" uniqKey="Tona G" first="G." last="Tona">G. Tona</name>
</country>
<country name="Belgique">
<region name="Province de Liège">
<name sortKey="Tits, M" sort="Tits, M" uniqKey="Tits M" first="M." last="Tits">M. Tits</name>
</region>
<name sortKey="Angenot, L" sort="Angenot, L" uniqKey="Angenot L" first="L." last="Angenot">L. Angenot</name>
<name sortKey="Frederich, M" sort="Frederich, M" uniqKey="Frederich M" first="M." last="Frederich">M. Frederich</name>
</country>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Sante/explor/ChloroquineV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 001761 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 001761 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Sante
   |area=    ChloroquineV1
   |flux=    Main
   |étape=   Exploration
   |type=    RBID
   |clé=     Pascal:10-0330894
   |texte=   In vitro and in vivo antimalarial and cytotoxic activity of five plants used in congolese traditional medicine
}}

Wicri

This area was generated with Dilib version V0.6.33.
Data generation: Wed Mar 25 22:43:59 2020. Site generation: Sun Jan 31 12:44:45 2021