Hostname: page-component-cd9895bd7-jn8rn Total loading time: 0 Render date: 2024-12-27T02:54:04.908Z Has data issue: false hasContentIssue false

In vitro sensitivity of artemeter in Plasmodium falciparum-infected beta-thalassaemic trait erythrocytes

Published online by Cambridge University Press:  01 February 1999

A. C. SENOK
Affiliation:
Department of Paediatrics, The Chinese University of Hong Kong, Shatin, NT, Hong Kong
K. LI
Affiliation:
Department of Paediatrics, The Chinese University of Hong Kong, Shatin, NT, Hong Kong
E. A. S. NELSON
Affiliation:
Department of Paediatrics, The Chinese University of Hong Kong, Shatin, NT, Hong Kong
K. W. CHUNG
Affiliation:
Department of Paediatrics, The Chinese University of Hong Kong, Shatin, NT, Hong Kong

Abstract

Using an age-fractionated RBC model, we investigated the in vitro sensitivity of artemether in β-thalassaemic RBC infected with the K1 and FC27 strains of Plasmodium falciparum and, to study the role of oxidant stress in modulating the sensitivity pattern, pro-oxidant (riboflavin) and antioxidant (vitamin E) agents were added to cultures in the presence of artemether. With the FC27 strain, the artemether IC50 doses in thalassaemic samples (whole blood and fractions) were significantly higher compared to equivalent normal RBC samples (P<0·05). However, with the K1 strain, such a significant difference was not demonstrable. The addition of vitamin E reduced the antimalarial effect of artemether in both the FC27 and K1 strains (P<0·0001). In contrast, the addition of riboflavin resulted in a significant increase in antimalarial activity (P<0·0001). This effect of the drug combinations was not influenced by the red cell type (P<0·0001) and there was no interaction between red cell type and drug type (P<0·0001). These findings show that reduced sensitivity to artemether occurs in whole blood and age-fractionated β-thalassaemic trait RBC. It appears that the RBC redox status does not influence the sensitivity to artemether.

Type
Research Article
Copyright
1999 Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)