TY - JOUR
T1 - Deleterious synergistic effects of ascorbate and copper on the development of Plasmodium falciparum
T2 - An in vitro study in normal and in G6PD-deficient erythrocytes
AU - Marva, Esther
AU - Cohen, Alona
AU - Saltman, Paul
AU - Chevion, Mordechai
AU - Golenser, Jacob
PY - 1989/11
Y1 - 1989/11
N2 - The effects of ascorbate and copper on the development of Plasmodium falciparum were studied in two modes: pretreatment of uninfected erythrocytes followed by infection by P. falciparum and treatment of parasitized erythrocytes. Pretreatment of G6PD(+) cells with ascorbate caused a slight enhancement in parasite development, while in G6PD(-) cells a suppressive effect on the plasmodia was demonstrated. Copper alone interfered with parasite growth in both cell types. The combination of copper and ascorbate arrested parasite maturation, an effect which was more pronounced in G6PD(-) cells. Synergism between copper and ascorbate was better demonstrated following the treatment of infected erythrocytes: while ascorbate alone supported parasite development and copper alone had only a marginal suppressive effect, the combination of copper and ascorbate yielded a marked inhibition of parasite growth. Ascorbate proved destructive to the parasites in the presence of adventitious copper, or on the second day of the parasite life cycle. In these cases it acted as a pro-oxidant, while in other systems, in particular in the presence of a chelator, ascorbate acted as an antioxidant and promoted parasite growth. The understanding of the role of transition metals and free radicals in parasite development and injury could shed light on novel approaches to fight malaria.
AB - The effects of ascorbate and copper on the development of Plasmodium falciparum were studied in two modes: pretreatment of uninfected erythrocytes followed by infection by P. falciparum and treatment of parasitized erythrocytes. Pretreatment of G6PD(+) cells with ascorbate caused a slight enhancement in parasite development, while in G6PD(-) cells a suppressive effect on the plasmodia was demonstrated. Copper alone interfered with parasite growth in both cell types. The combination of copper and ascorbate arrested parasite maturation, an effect which was more pronounced in G6PD(-) cells. Synergism between copper and ascorbate was better demonstrated following the treatment of infected erythrocytes: while ascorbate alone supported parasite development and copper alone had only a marginal suppressive effect, the combination of copper and ascorbate yielded a marked inhibition of parasite growth. Ascorbate proved destructive to the parasites in the presence of adventitious copper, or on the second day of the parasite life cycle. In these cases it acted as a pro-oxidant, while in other systems, in particular in the presence of a chelator, ascorbate acted as an antioxidant and promoted parasite growth. The understanding of the role of transition metals and free radicals in parasite development and injury could shed light on novel approaches to fight malaria.
KW - ascorbic acid
KW - copper
KW - free radicals
KW - G6PD deficiency
KW - Plasmodium falciparum
UR - http://www.scopus.com/inward/record.url?scp=0024791882&partnerID=8YFLogxK
U2 - 10.1016/0020-7519(89)90066-0
DO - 10.1016/0020-7519(89)90066-0
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C2 - 2687184
AN - SCOPUS:0024791882
SN - 0020-7519
VL - 19
SP - 779
EP - 785
JO - International Journal for Parasitology
JF - International Journal for Parasitology
IS - 7
ER -