Oral artesunate prevents Plasmodium berghei Anka infection in mice

被引:15
作者
Gumede, B
Folb, P
Ryffel, B
机构
[1] Univ Cape Town, Dept Immunol, ZA-7925 Cape Town, South Africa
[2] Univ Cape Town, Dept Pharmacol, Cape Town, South Africa
[3] CNRS, Inst Transgenose, Orleans, France
基金
新加坡国家研究基金会;
关键词
malaria; Plasmodium berghei; chloroquine; artesunate;
D O I
10.1016/S1383-5769(02)00081-8
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Artesunate, a semi-synthetic derivative of a naturally occurring anti-malarial artemisinin was compared with chloroquine in C57BL/6 mice infected with Plasmodium berghei Anka (PbA). A 7-day oral administration of artesunate prevented parasitaemia at 10 mg/kg/day. However, recrudescence of parasitaemia and cerebral malaria occurred upon cessation of treatment followed by death within 28 days. However, a 14-day course of artesunate (100 mg/kg/day) prevented completely the development of parasitaemia and cerebral malaria with a survival of more than 60-days as did 10 mg/kg/day chloroquine. These data demonstrate that oral artesunate inhibits PbA and prevents cerebral malaria, but needs to be administered at high dose and for prolonged time to eradicate PbA infection in mice. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:53 / 59
页数:7
相关论文
共 18 条
[1]  
BUNNAG D, 1991, Southeast Asian Journal of Tropical Medicine and Public Health, V22, P534
[2]  
Clark I A, 1992, Immunol Ser, V56, P365
[3]  
Dhingra V, 1999, LIFE SCI, V66, P279, DOI 10.1016/S0024-3205(99)00356-2
[4]   TRANSGENIC MICE EXPRESSING HIGH-LEVELS OF SOLUBLE TNF-R1 FUSION PROTEIN ARE PROTECTED FROM LETHAL SEPTIC SHOCK AND CEREBRAL MALARIA, AND ARE HIGHLY SENSITIVE TO LISTERIA-MONOCYTOGENES AND LEISHMANIA-MAJOR INFECTIONS [J].
GARCIA, I ;
MIYAZAKI, Y ;
ARAKI, K ;
ARAKI, M ;
LUCAS, R ;
GRAU, GE ;
MILON, G ;
BELKAID, Y ;
MONTIXI, C ;
LESSLAUER, W ;
VASSALLI, P .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1995, 25 (08) :2401-2407
[5]   Metabolism of artelinic acid to dihydroqinghaosu by human liver cytochrome P4503A [J].
Grace, JM ;
Skanchy, DJ ;
Aguilar, AJ .
XENOBIOTICA, 1999, 29 (07) :703-717
[6]   TUMOR-NECROSIS-FACTOR (CACHECTIN) AS AN ESSENTIAL MEDIATOR IN MURINE CEREBRAL MALARIA [J].
GRAU, GE ;
FAJARDO, LF ;
PIGUET, PF ;
ALLET, B ;
LAMBERT, PH ;
VASSALLI, P .
SCIENCE, 1987, 237 (4819) :1210-1212
[7]  
Jeong JY, 1997, J IMMUNOL, V158, P4901
[8]  
KARBWANG J, 1994, B WORLD HEALTH ORGAN, V72, P233
[9]   Chloroquine inhibits proinflammatory cytokine release into human whole blood [J].
Karres, I ;
Kremer, JP ;
Dietl, I ;
Steckholzer, U ;
Jochum, M ;
Ertel, W .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1998, 274 (04) :R1058-R1064
[10]   TRANSDERMAL ARTELINIC ACID - AN EFFECTIVE TREATMENT FOR PLASMODIUM-BERGHEI-INFECTED MICE [J].
KLAYMAN, DL ;
AGER, AL ;
FLECKENSTEIN, L ;
LIN, AJ .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1991, 45 (05) :602-607