Suppressive effects of the anti-oxidant N-acetylcysteine on the anti-malarial activity of artesunate

被引:20
作者
Arreesrisom, Peera
Dondorp, Arjen M.
Looareesuwan, Sornchai
Udomsangpetch, Rachanee [1 ]
机构
[1] Mahidol Univ, Fac Sci, Dept Pathobiol, Bangkok 10400, Thailand
[2] Mahidol Univ, Fac Trop Med, Hosp Trop Dis, Bangkok 10400, Thailand
[3] Univ Oxford, John Radcliffe Hosp, Nuffield Dept Clin Med, Ctr Trop Med, Oxford OX3 9DU, England
基金
英国惠康基金;
关键词
P; falciparum; combined anti-malarials; drug resistance;
D O I
10.1016/j.parint.2007.04.004
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
The anti-oxidant drug N-acetylcysteine (NAC) has been proposed as adjunctive treatment in severe falciparum malaria. However, this might inhibit the anti-malarial drug action of the artemisinins, which are thought to exert their parasitocidal action through oxidative damage. We studied the interaction between NAC and artesunate as well as quinine in an in vitro drug sensitivity assay. Combination with NAC reduced the parasitocidal effect of artesunate only within the first 6 h of incubation, whereas no interaction was observed with quinine. Pre-incubation of P. falciparum with NAC resulted in a similar inhibitory effect on the anti-malarial activity of artesunate, whereas no inhibition was observed when NAC was added 2 h after parasite exposure to artesunate. Assessment of parasite maturation inhibition by the standard Giemsa's staining was in accordance with the use of a vital staining. The results herein caution the use of adjunctive treatment for malaria infection. Combination of antagonistic drugs may lead to adverse effects. (c) 2007 Elsevier Ireland Ltd. All tights reserved.
引用
收藏
页码:221 / 226
页数:6
相关论文
共 18 条
[1]   The malaria parasite supplies glutathione to its host cell -: Investigation of glutathione transport and metabolism in human erythrocytes infected with Plasmodium falciparum [J].
Atamna, H ;
Ginsburg, H .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1997, 250 (03) :670-679
[2]   Plasmodium falciparum glutathione metabolism and growth are independent of glutathione system of host erythrocyte [J].
Ayi, K ;
Cappadoro, M ;
Branca, M ;
Turrini, F ;
Arese, P .
FEBS LETTERS, 1998, 424 (03) :257-261
[3]  
Beales PF, 2000, T ROY SOC TROP MED H, V94, pS1
[4]   Oxidative stress in malaria parasite-infected erythrocytes: host-parasite interactions [J].
Becker, K ;
Tilley, L ;
Vennerstrom, JL ;
Roberts, D ;
Rogerson, S ;
Ginsburg, H .
INTERNATIONAL JOURNAL FOR PARASITOLOGY, 2004, 34 (02) :163-189
[5]   GENERATION OF REACTIVE OXYGEN SPECIES IN WHOLE-BLOOD FROM PATIENTS WITH ACUTE FALCIPARUM-MALARIA [J].
DESCAMPSLATSCHA, B ;
LUNELFABIANI, F ;
KARABINIS, A ;
DRUILHE, P .
PARASITE IMMUNOLOGY, 1987, 9 (02) :275-279
[6]   Oxidative stress and rheology in severe malaria [J].
Dondorp, AM ;
Omodeo-Salè, F ;
Chotivanich, K ;
Taramelli, D ;
White, NJ .
REDOX REPORT, 2003, 8 (05) :292-294
[7]   Mechanisms of in situ activation for peroxidic antimalarials [J].
Dong, YX ;
Vennerstrom, JL .
REDOX REPORT, 2003, 8 (05) :284-288
[8]   Artemisinins target the SERCA of Plasmodium falciparum [J].
Eckstein-Ludwig, U ;
Webb, RJ ;
van Goethem, IDA ;
East, JM ;
Lee, AG ;
Kimura, M ;
O'Neill, PM ;
Bray, PG ;
Ward, SA ;
Krishna, S .
NATURE, 2003, 424 (6951) :957-961
[9]  
Faiz MA, 2005, LANCET, V366, P717
[10]   Glucose is toxic to glycosome-deficient trypanosomes [J].
Furuya, T ;
Kessler, P ;
Jardim, A ;
Schnaufer, A ;
Crudder, C ;
Parsons, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (22) :14177-14182