INVITRO AND INVIVO LEISHMANICIDAL ACTIVITES OF NATURAL AND SYNTHETIC QUINOIDS

被引:38
作者
SAUVAIN, M
DEDET, JP
KUNESCH, N
POISSON, J
GANTIER, JC
GAYRAL, P
KUNESCH, G
机构
[1] FAC MED MONTPELLIER,ECOL MED & PATHOL PARISITAIRE LAB,F-34000 MONTPELLIER,FRANCE
[2] FAC PHARM CHATENAY MALABRY,CHIM SUBST THERAPEUT NAT LAB,CNRS,SDI 6233,F-92296 CHATENAY MALABRY,FRANCE
[3] FAC PHARM CHATENAY MALABRY,PARASITOL LAB,F-92296 CHATENAY MALABRY,FRANCE
[4] UNIV PARIS 11,CHIM COORDINAT BIOORGAN & BIOINORGAN LAB,CNRS,URA 1384,F-91405 ORSAY,FRANCE
[5] FAC PHARM CHATENAY MALABRY,CHIM LAB SUBST THERAPEUT NAT LAB,CNRS,URA 130,F-92296 CHATENAY MALABRY,FRANCE
关键词
ANTILEISHMANIALS; LEISHMANIA-AMAZONESIS; JACARANDA-COPAIA; JACARANONE; URSOLIC ACID; QUINOL ACETATES; QUINONE ACETATES;
D O I
10.1002/ptr.2650070215
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The activities of various compounds isolated from plants traditionally used against leishmaniasis in populations from the tablelands of the Guyanas have been examined. The leishmanicidal activity of plant extracts was evaluated by in vitro testing on promastigote and amastigote stages of Leishmania amazonensis and by in vivo tests on L. amazonensis in mice. The leaves of Jacaranda copaia (Aublet) D. Don yielded two compounds: ursolic acid and jaracanone. Ursolic acid showed an interesting activity in vitro with an ED50 against amastigotes of 0.02 mm and no toxicity to macrophages at twice this dose. Jacaranone displayed a marked activity against promastigotes in vitro with an ED50 of 0.02 mm. Both compounds have weak in vivo antileishmanial activity. Similar synthetic compounds such as quinol and quinone acetates were prepared and showed increased activity in experimental cutaneous leishmaniasis in mice.
引用
收藏
页码:167 / 171
页数:5
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