Antileishmanial activity of furoquinolines and coumarins from Helietta apiculata

被引:69
作者
Elena Ferreira, Maria [2 ]
Rojas de Arias, Antonieta [3 ]
Yaluff, Gloria [2 ]
Vera de Bilbao, Ninfa [2 ]
Nakayama, Hector [2 ]
Torres, Susana [2 ]
Schinini, Alicia [2 ]
Guy, Isabelle [4 ]
Heinzen, Horacio [5 ]
Fournet, Alain [1 ]
机构
[1] Fac Pharm Chatenay Malabry, Lab Pharmacognosie, IRD US 084, F-92296 Chatenay Malabry, France
[2] Inst Invest Ciencias Salud, Dept Trop Med, Asuncion, Paraguay
[3] CEDIC FMB Diaz Gill Med Lab, Asuncion, Paraguay
[4] Univ Angers, Fac Pharm, Angers, France
[5] Fac Quim Montevideo, Catedra Farmacognosia & Prod Nat, Montevideo, Uruguay
关键词
Helietta apiculata; Rutaceae; Furoquinolines; Coumarins; Leishmania amazonensis; Oral administration; IN-VITRO; ALKALOIDS; METABOLISM; VIVO;
D O I
10.1016/j.phymed.2009.09.009
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The bark infusion of H. apiculata are used to treat wound healing related to cutaneous leishmaniasis and as anti-inflammatory. Aim of the study: To isolate, purify active constituents of H. apiculata stem bark, and evaluate their in vitro and in vivo antileishmanial activities. Materials and methods: Isolation by chromatographic methods and chemical identification of furoquinoline alkaloids and coumarins, then evaluation of the in vitro leishmanicidal activity of these compounds against three strains of Leishmania sp. promastigotes and in vivo against Leigh mania amazonensis in Balb/c mice. Results: Furoquinoline alkaloids and coumarins presented a moderate in vitro activity against promastigote forms of Leishmania sp. with IC50 values in the range between 17 and > 50 mu g/ml. Balb/c mice infected with Leishmania amazonensis were treated with gamma-fagarine by oral route, or with 3-(1'-dimethylallyl)-decursinol or (-)-heliettin by subscutaneous route for 14 days at 10 mg/kg daily. In these conditions, gamma-fagarine, 3-(1'-dimethylally1)-decursinol and (-)-heliettin showed the same efficacy as the reference drug reducing by 97.4, 95.6 and 98.6% the parasite loads in the lesion, respectively. Conclusion: These compounds showed significant efficacy in L amazonensis infected mice, providing important knowledge to improve its potential role for a future use in the treatment of cutaneous leishmaniasis. (C) 2009 Elsevier GmbH. All rights reserved.
引用
收藏
页码:375 / 378
页数:4
相关论文
共 21 条
[1]  
[Anonymous], 2007, GUIDELINES EUTHANASI
[2]   High-throughput screening for stability and inhibitory activity of compounds toward cytochrome P450-mediated metabolism [J].
Ansede, JH ;
Thakker, DR .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2004, 93 (02) :239-255
[3]   CULTURE MICROTITRATION - A SENSITIVE METHOD FOR QUANTIFYING LEISHMANIA-INFANTUM IN TISSUES OF INFECTED MICE [J].
BUFFET, PA ;
SULAHIAN, A ;
GARIN, YJF ;
NASSAR, N ;
DEROUIN, F .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (09) :2167-2168
[4]   Oxidizing species in the mechanism of cytochrome P450 [J].
de Montellano, PRO ;
De Voss, JJ .
NATURAL PRODUCT REPORTS, 2002, 19 (04) :477-493
[5]   Metabolism of 2-substituted quinolines with antileishmanial activity studied in vitro with liver microsomes, hepatocytes and recombinantly expressed enzymes analyzed by LC/MS [J].
Desrivot, Julie ;
Edlund, Per-Olof ;
Svensson, Richard ;
Baranczewski, Pawel ;
Fournet, Alain ;
Figadere, Bruno ;
Herrenknecht, Christine .
TOXICOLOGY, 2007, 235 (1-2) :27-38
[6]   COUMARINS AND ALKALOIDS OF GENUS PTELEA [J].
DREYER, DL .
PHYTOCHEMISTRY, 1969, 8 (06) :1013-&
[7]   2-SUBSTITUTED QUINOLINE ALKALOIDS AS POTENTIAL ANTILEISHMANIAL DRUGS [J].
FOURNET, A ;
BARRIOS, AA ;
MUNOZ, V ;
HOCQUEMILLER, R ;
CAVE, A ;
BRUNETON, J .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1993, 37 (04) :859-863
[8]  
GALAN RH, 1988, HETEROCYCLES, V27, P775
[9]   Inhibition of cytochrome P450-dependent monooxygenases by an alkaloid fraction from Helietta apiculata markedly potentiate the hypnotic action of pentobarbital [J].
Goloubkova, TD ;
Heckler, E ;
Rates, SMK ;
Henriques, JAP ;
Henriques, AT .
JOURNAL OF ETHNOPHARMACOLOGY, 1998, 60 (02) :141-148
[10]  
Gray A. I., 1993, Methods in Biochemistry, V8, P271