Antiplasmodial activity of aryltetralone lignans from Holostylis reniformis

被引:28
作者
de Andrade-Neto, Valter F.
da Silva, Tito
Xavier Lopes, Lucia M.
do Rosario, Virgilio E.
de Pilla Varotti, Fernando
Krettli, Antoniana U.
机构
[1] Univ Estadual Paulista, Inst Quim, BR-14801970 Araraquara, SP, Brazil
[2] Fiocruz MS, Ctr Pesquisas Rene Rachou, Lab Malaria, BR-30190002 Belo Horizonte, MG, Brazil
[3] Univ Fed Minas Gerais, Dept Parasitol, BR-30190002 Belo Horizonte, MG, Brazil
[4] Univ Nova Lisboa, Inst Hyg & Med Trop, Ctr Malaria & Doencas Trop, P-1349 Lisbon, Portugal
关键词
D O I
10.1128/AAC.01344-06
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Extracts from Holostylis reniformis were tested in vivo against Plasmodium berghei and in vitro against a chloroquine-resistant strain of Plasmodium falciparum. The hexane extract of the roots was the most active, causing 67% reduction of parasitemia in vivo. From this extract, six lignans, including a new (7 ' R,8S,8 ' S)-3 ',4 '-methylenedioxy-4,5-dimethoxy-2,7 '-cyclolignan-7-one, were isolated and tested in vitro against P. falciparum. The three most active lignans showed 50% inhibitor concentrations of <= 0.32 mu M. An evaluation of minimum lethal dose (30%) values showed low toxicity for these lignans in a hepatic cell line (Hep G2A16). Therefore, these compounds are potential candidates for the development of antimalarial drugs.
引用
收藏
页码:2346 / 2350
页数:5
相关论文
共 28 条
[1]   Antimalarial activity of Bidens pilosa L. (Asteraceae) ethanol extracts from wild plants collected in various localities or plants cultivated in humus soil [J].
Andrade-Neto, VF ;
Brandao, MGL ;
Oliveira, FQ ;
Casali, VWD ;
Njaine, B ;
Zalis, MG ;
Oliveira, LA ;
Krettli, AU .
PHYTOTHERAPY RESEARCH, 2004, 18 (08) :634-639
[2]  
[Anonymous], 1999, Comprehensive Natural Products Chemistry
[3]   Lignans and neolignans as lead compounds [J].
S. Apers ;
A. Vlietinck ;
L. Pieters .
Phytochemistry Reviews, 2003, 2 (3) :201-217
[4]  
CARVALHO LH, 1991, BRAZ J MED BIOL RES, V24, P1113
[5]   Aryltetralone lignans and 7,8-seco-lignans from Holostylis reniformis [J].
da Silva, T ;
Lopes, LM .
PHYTOCHEMISTRY, 2004, 65 (06) :751-759
[6]  
da Silva T., 2005, REV PROP IND, V1795, P1774
[7]   Aryltetralol and aryltetralone lignans from Holostylis reniformis [J].
Da Silva, Tito ;
Lopes, Lucia M. X. .
PHYTOCHEMISTRY, 2006, 67 (09) :929-937
[8]   Antimalarial activity of medicinal plants used in traditional medicine in S. Tome and Principe islands [J].
de Madureira, MD ;
Martins, AP ;
Gomes, M ;
Paiva, J ;
da Cunha, AP ;
do Rosário, V .
JOURNAL OF ETHNOPHARMACOLOGY, 2002, 81 (01) :23-29
[9]   Configurational analysis of cubebins and bicubebin from Aristolochia lagesiana and Aristolochia pubescens [J].
de Pascoli, IC ;
Nascimento, IR ;
Lopes, LMX .
PHYTOCHEMISTRY, 2006, 67 (07) :735-742
[10]   RAPID COLORIMETRIC ASSAY FOR CELL-GROWTH AND SURVIVAL - MODIFICATIONS TO THE TETRAZOLIUM DYE PROCEDURE GIVING IMPROVED SENSITIVITY AND RELIABILITY [J].
DENIZOT, F ;
LANG, R .
JOURNAL OF IMMUNOLOGICAL METHODS, 1986, 89 (02) :271-277