Antiprotozoal activity of quinoline alkaloids isolated from Galipea longiflora, a Bolivian plant used as a treatment for cutaneous leishmaniasis
Identifieur interne : 00AC09 ( Main/Exploration ); précédent : 00AC08; suivant : 00AC10Antiprotozoal activity of quinoline alkaloids isolated from Galipea longiflora, a Bolivian plant used as a treatment for cutaneous leishmaniasis
Auteurs : A. Fournet [France] ; A. Angelo Barrios ; V. Mu Oz ; R. Hocquemiller [France] ; F. Roblot [France] ; A. Cavé [France] ; P. Richomme [France] ; J. Bruneton [France]Source :
- Phytotherapy Research [ 0951-418X ] ; 1994-05.
Descripteurs français
- Wicri :
- topic : Bolivie.
English descriptors
- KwdEn :
- Alkaloid, Alkaloidal, Amazonensis, Antiprotozoal activity, Balblc mice, Bolivia, Chimane, Chimane indians, Chimanine, Control mice, Crude alkaloidal extracts, Cruzi, Cutaneous, Cutaneous leishmaniasis, Epimastigote forms, First experiment, Fournet, Galipea, Galipea longiflora, Glucantime, Leishmania, Leishmania amazonensis, Leishmania species, Leishmaniasis, Lesion, Longiflora, Parasite, Plant material, Promastigote forms, Quinoline, Quinoline alkaloids, Rear footpad, Reference drug, Root bark, Trypanosoma, Trypanosoma cruzi, Uitro, Uitro activity.
- Teeft :
- Alkaloid, Alkaloidal, Amazonensis, Antiprotozoal activity, Balblc mice, Bolivia, Chimane, Chimane indians, Chimanine, Control mice, Crude alkaloidal extracts, Cruzi, Cutaneous, Cutaneous leishmaniasis, Epimastigote forms, First experiment, Fournet, Galipea, Galipea longiflora, Glucantime, Leishmania, Leishmania amazonensis, Leishmania species, Leishmaniasis, Lesion, Longiflora, Parasite, Plant material, Promastigote forms, Quinoline, Quinoline alkaloids, Rear footpad, Reference drug, Root bark, Trypanosoma, Trypanosoma cruzi, Uitro, Uitro activity.
Abstract
The stem bark of Galipea longiflora is used by the Chimane Indians in Bolivia for the treatment of cutaneous leishmaniasis produced by Leishmania braziliensis. Petroleum ether and chloroform extracts of stem, root bark and leaves were found active in vitro against Leishmania ssp and Trypanosoma cruzi at 100 μg/mL. The activity guided fractionation of the extracts by chromatography afforded 12 active compounds identified as 2‐substituted quinoline alkaloids. BALB/c mice were infected with Leishmania amazonensis (strain PH8 or H‐142) and treated 24 h after infection with the major alkaloids from the crude alkaloidal extract; 2‐phenylquinoline and 2‐n‐pentylquinoline. 2‐phenylquinoline was as potent as Glucantime (Rhǒne‐Poulenc) against the strain H‐142, but less active than the reference drug against the virulent strain PH8 of L. amazonensis. 2‐n‐pentylquinoline did not exhibit any activity. Assays of single local treatments on the rear footpad infection, 2 weeks after the parasitic inoculation, indicated an effect for 2‐phenylquinoline by reducing the severity of lesion. However, this activity was found to be slightly lower than that obtained using Glucantime.
Url:
DOI: 10.1002/ptr.2650080312
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 001535
- to stream Istex, to step Curation: 001535
- to stream Istex, to step Checkpoint: 005072
- to stream Main, to step Merge: 00B252
- to stream Main, to step Curation: 00AC09
Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Antiprotozoal activity of quinoline alkaloids isolated from Galipea longiflora, a Bolivian plant used as a treatment for cutaneous leishmaniasis</title>
<author><name sortKey="Fournet, A" sort="Fournet, A" uniqKey="Fournet A" first="A." last="Fournet">A. Fournet</name>
</author>
<author><name sortKey="Barrios, A Angelo" sort="Barrios, A Angelo" uniqKey="Barrios A" first="A. Angelo" last="Barrios">A. Angelo Barrios</name>
</author>
<author><name sortKey="Mu Oz, V" sort="Mu Oz, V" uniqKey="Mu Oz V" first="V." last="Mu Oz">V. Mu Oz</name>
</author>
<author><name sortKey="Hocquemiller, R" sort="Hocquemiller, R" uniqKey="Hocquemiller R" first="R." last="Hocquemiller">R. Hocquemiller</name>
</author>
<author><name sortKey="Roblot, F" sort="Roblot, F" uniqKey="Roblot F" first="F." last="Roblot">F. Roblot</name>
</author>
<author><name sortKey="Cave, A" sort="Cave, A" uniqKey="Cave A" first="A." last="Cavé">A. Cavé</name>
</author>
<author><name sortKey="Richomme, P" sort="Richomme, P" uniqKey="Richomme P" first="P." last="Richomme">P. Richomme</name>
</author>
<author><name sortKey="Bruneton, J" sort="Bruneton, J" uniqKey="Bruneton J" first="J." last="Bruneton">J. Bruneton</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:2BC18EB9713CB6FD5A474A94A2FE4F8602C418A0</idno>
<date when="1994" year="1994">1994</date>
<idno type="doi">10.1002/ptr.2650080312</idno>
<idno type="url">https://api.istex.fr/document/2BC18EB9713CB6FD5A474A94A2FE4F8602C418A0/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">001535</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">001535</idno>
<idno type="wicri:Area/Istex/Curation">001535</idno>
<idno type="wicri:Area/Istex/Checkpoint">005072</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Checkpoint">005072</idno>
<idno type="wicri:doubleKey">0951-418X:1994:Fournet A:antiprotozoal:activity:of</idno>
<idno type="wicri:Area/Main/Merge">00B252</idno>
<idno type="wicri:Area/Main/Curation">00AC09</idno>
<idno type="wicri:Area/Main/Exploration">00AC09</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Antiprotozoal activity of quinoline alkaloids isolated from <hi rend="italic">Galipea longiflora</hi>
, a Bolivian plant used as a treatment for cutaneous leishmaniasis</title>
<author><name sortKey="Fournet, A" sort="Fournet, A" uniqKey="Fournet A" first="A." last="Fournet">A. Fournet</name>
<affiliation wicri:level="1"><country xml:lang="fr">France</country>
<wicri:regionArea>Institut Français de Recherche Scientifique pour le Développement en Coopération (ORSTOM), Département Santé, 213, rue La Fayette, 75480 Paris, Cédex 10</wicri:regionArea>
<wicri:noRegion>Cédex 10</wicri:noRegion>
<wicri:noRegion>Cédex 10</wicri:noRegion>
</affiliation>
<affiliation wicri:level="1"><country xml:lang="fr">France</country>
<wicri:regionArea>Correspondence address: Institut Français de Recherche Scientifique pour le Développement en Coopération (ORSTOM), Département Santé, 213, rue La Fayette, 75480 Paris, Cédex 10</wicri:regionArea>
<wicri:noRegion>Cédex 10</wicri:noRegion>
<wicri:noRegion>Cédex 10</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Barrios, A Angelo" sort="Barrios, A Angelo" uniqKey="Barrios A" first="A. Angelo" last="Barrios">A. Angelo Barrios</name>
<affiliation><wicri:noCountry code="subField">Bolivia</wicri:noCountry>
</affiliation>
</author>
<author><name sortKey="Mu Oz, V" sort="Mu Oz, V" uniqKey="Mu Oz V" first="V." last="Mu Oz">V. Mu Oz</name>
<affiliation><wicri:noCountry code="subField">Bolivia</wicri:noCountry>
</affiliation>
</author>
<author><name sortKey="Hocquemiller, R" sort="Hocquemiller, R" uniqKey="Hocquemiller R" first="R." last="Hocquemiller">R. Hocquemiller</name>
<affiliation wicri:level="4"><country xml:lang="fr">France</country>
<wicri:regionArea>Laboratoire de Pharmacognosie, associé au CNRS, Faculté de Pharmacie, Université Paris XI, 92296 Chǎtenay‐Malabry, Cedex</wicri:regionArea>
<orgName type="university">Université Paris-Sud</orgName>
<placeName><settlement type="city">Orsay</settlement>
<region type="region" nuts="2">Île-de-France</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Roblot, F" sort="Roblot, F" uniqKey="Roblot F" first="F." last="Roblot">F. Roblot</name>
<affiliation wicri:level="4"><country xml:lang="fr">France</country>
<wicri:regionArea>Laboratoire de Pharmacognosie, associé au CNRS, Faculté de Pharmacie, Université Paris XI, 92296 Chǎtenay‐Malabry, Cedex</wicri:regionArea>
<orgName type="university">Université Paris-Sud</orgName>
<placeName><settlement type="city">Orsay</settlement>
<region type="region" nuts="2">Île-de-France</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Cave, A" sort="Cave, A" uniqKey="Cave A" first="A." last="Cavé">A. Cavé</name>
<affiliation wicri:level="4"><country xml:lang="fr">France</country>
<wicri:regionArea>Laboratoire de Pharmacognosie, associé au CNRS, Faculté de Pharmacie, Université Paris XI, 92296 Chǎtenay‐Malabry, Cedex</wicri:regionArea>
<orgName type="university">Université Paris-Sud</orgName>
<placeName><settlement type="city">Orsay</settlement>
<region type="region" nuts="2">Île-de-France</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Richomme, P" sort="Richomme, P" uniqKey="Richomme P" first="P." last="Richomme">P. Richomme</name>
<affiliation wicri:level="1"><country xml:lang="fr">France</country>
<wicri:regionArea>Centre d'Etude des Plantes Médicinales, Unité d'Enseignement et de Recherche des Sciences Médicales et Pharmaceutiques, 16 Bd Daviers, 49000 Angers</wicri:regionArea>
<wicri:noRegion>49000 Angers</wicri:noRegion>
<wicri:noRegion>49000 Angers</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Bruneton, J" sort="Bruneton, J" uniqKey="Bruneton J" first="J." last="Bruneton">J. Bruneton</name>
<affiliation wicri:level="3"><country xml:lang="fr">France</country>
<wicri:regionArea>Centre d'Etude des Plantes Médicinales, Unité d'Enseignement et de Recherche des Sciences Médicales et Pharmaceutiques, 16 Bd Daviers, 49000 Angers</wicri:regionArea>
<placeName><region type="region" nuts="2">Pays de la Loire</region>
<settlement type="city">Angers</settlement>
</placeName>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series><title level="j" type="main">Phytotherapy Research</title>
<title level="j" type="alt">PHYTOTHERAPY RESEARCH</title>
<idno type="ISSN">0951-418X</idno>
<idno type="eISSN">1099-1573</idno>
<imprint><biblScope unit="vol">8</biblScope>
<biblScope unit="issue">3</biblScope>
<biblScope unit="page" from="174">174</biblScope>
<biblScope unit="page" to="178">178</biblScope>
<biblScope unit="page-count">5</biblScope>
<publisher>John Wiley & Sons, Ltd.</publisher>
<pubPlace>Chichester, UK</pubPlace>
<date type="published" when="1994-05">1994-05</date>
</imprint>
<idno type="ISSN">0951-418X</idno>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt><idno type="ISSN">0951-418X</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Alkaloid</term>
<term>Alkaloidal</term>
<term>Amazonensis</term>
<term>Antiprotozoal activity</term>
<term>Balblc mice</term>
<term>Bolivia</term>
<term>Chimane</term>
<term>Chimane indians</term>
<term>Chimanine</term>
<term>Control mice</term>
<term>Crude alkaloidal extracts</term>
<term>Cruzi</term>
<term>Cutaneous</term>
<term>Cutaneous leishmaniasis</term>
<term>Epimastigote forms</term>
<term>First experiment</term>
<term>Fournet</term>
<term>Galipea</term>
<term>Galipea longiflora</term>
<term>Glucantime</term>
<term>Leishmania</term>
<term>Leishmania amazonensis</term>
<term>Leishmania species</term>
<term>Leishmaniasis</term>
<term>Lesion</term>
<term>Longiflora</term>
<term>Parasite</term>
<term>Plant material</term>
<term>Promastigote forms</term>
<term>Quinoline</term>
<term>Quinoline alkaloids</term>
<term>Rear footpad</term>
<term>Reference drug</term>
<term>Root bark</term>
<term>Trypanosoma</term>
<term>Trypanosoma cruzi</term>
<term>Uitro</term>
<term>Uitro activity</term>
</keywords>
<keywords scheme="Teeft" xml:lang="en"><term>Alkaloid</term>
<term>Alkaloidal</term>
<term>Amazonensis</term>
<term>Antiprotozoal activity</term>
<term>Balblc mice</term>
<term>Bolivia</term>
<term>Chimane</term>
<term>Chimane indians</term>
<term>Chimanine</term>
<term>Control mice</term>
<term>Crude alkaloidal extracts</term>
<term>Cruzi</term>
<term>Cutaneous</term>
<term>Cutaneous leishmaniasis</term>
<term>Epimastigote forms</term>
<term>First experiment</term>
<term>Fournet</term>
<term>Galipea</term>
<term>Galipea longiflora</term>
<term>Glucantime</term>
<term>Leishmania</term>
<term>Leishmania amazonensis</term>
<term>Leishmania species</term>
<term>Leishmaniasis</term>
<term>Lesion</term>
<term>Longiflora</term>
<term>Parasite</term>
<term>Plant material</term>
<term>Promastigote forms</term>
<term>Quinoline</term>
<term>Quinoline alkaloids</term>
<term>Rear footpad</term>
<term>Reference drug</term>
<term>Root bark</term>
<term>Trypanosoma</term>
<term>Trypanosoma cruzi</term>
<term>Uitro</term>
<term>Uitro activity</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Bolivie</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">The stem bark of Galipea longiflora is used by the Chimane Indians in Bolivia for the treatment of cutaneous leishmaniasis produced by Leishmania braziliensis. Petroleum ether and chloroform extracts of stem, root bark and leaves were found active in vitro against Leishmania ssp and Trypanosoma cruzi at 100 μg/mL. The activity guided fractionation of the extracts by chromatography afforded 12 active compounds identified as 2‐substituted quinoline alkaloids. BALB/c mice were infected with Leishmania amazonensis (strain PH8 or H‐142) and treated 24 h after infection with the major alkaloids from the crude alkaloidal extract; 2‐phenylquinoline and 2‐n‐pentylquinoline. 2‐phenylquinoline was as potent as Glucantime (Rhǒne‐Poulenc) against the strain H‐142, but less active than the reference drug against the virulent strain PH8 of L. amazonensis. 2‐n‐pentylquinoline did not exhibit any activity. Assays of single local treatments on the rear footpad infection, 2 weeks after the parasitic inoculation, indicated an effect for 2‐phenylquinoline by reducing the severity of lesion. However, this activity was found to be slightly lower than that obtained using Glucantime.</div>
</front>
</TEI>
<affiliations><list><country><li>France</li>
</country>
<region><li>Pays de la Loire</li>
<li>Île-de-France</li>
</region>
<settlement><li>Angers</li>
<li>Orsay</li>
</settlement>
<orgName><li>Université Paris-Sud</li>
</orgName>
</list>
<tree><noCountry><name sortKey="Barrios, A Angelo" sort="Barrios, A Angelo" uniqKey="Barrios A" first="A. Angelo" last="Barrios">A. Angelo Barrios</name>
<name sortKey="Mu Oz, V" sort="Mu Oz, V" uniqKey="Mu Oz V" first="V." last="Mu Oz">V. Mu Oz</name>
</noCountry>
<country name="France"><noRegion><name sortKey="Fournet, A" sort="Fournet, A" uniqKey="Fournet A" first="A." last="Fournet">A. Fournet</name>
</noRegion>
<name sortKey="Bruneton, J" sort="Bruneton, J" uniqKey="Bruneton J" first="J." last="Bruneton">J. Bruneton</name>
<name sortKey="Cave, A" sort="Cave, A" uniqKey="Cave A" first="A." last="Cavé">A. Cavé</name>
<name sortKey="Fournet, A" sort="Fournet, A" uniqKey="Fournet A" first="A." last="Fournet">A. Fournet</name>
<name sortKey="Hocquemiller, R" sort="Hocquemiller, R" uniqKey="Hocquemiller R" first="R." last="Hocquemiller">R. Hocquemiller</name>
<name sortKey="Richomme, P" sort="Richomme, P" uniqKey="Richomme P" first="P." last="Richomme">P. Richomme</name>
<name sortKey="Roblot, F" sort="Roblot, F" uniqKey="Roblot F" first="F." last="Roblot">F. Roblot</name>
</country>
</tree>
</affiliations>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/EdenteV2/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 00AC09 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 00AC09 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Santé |area= EdenteV2 |flux= Main |étape= Exploration |type= RBID |clé= ISTEX:2BC18EB9713CB6FD5A474A94A2FE4F8602C418A0 |texte= Antiprotozoal activity of quinoline alkaloids isolated from Galipea longiflora, a Bolivian plant used as a treatment for cutaneous leishmaniasis }}
This area was generated with Dilib version V0.6.32. |