Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/84502
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Type: Journal article
Title: Degrees of chloroquine resistance in Plasmodium - Is the redox system involved?
Author: Lehane, A.
McDevitt, C.
Kirk, K.
Fidock, D.
Citation: International Journal for Parasitology: Drugs and Drug Resistance, 2012; 2:47-57
Publisher: Elsevier
Issue Date: 2012
ISSN: 2211-3207
2211-3207
Statement of
Responsibility: 
Adele M. Lehane, Christopher A. McDevitt, Kiaran Kirk, David A. Fidock
Abstract: Chloroquine (CQ) was once a very effective antimalarial drug that, at its peak, was consumed in the hundreds of millions of doses per year. The drug acts against the Plasmodium parasite during the asexual intra-erythrocytic phase of its lifecycle. Unfortunately, clinical resistance to this drug is now widespread. Questions remain about precisely how CQ kills malaria parasites, and by what means some CQ-resistant (CQR) parasites can withstand much higher concentrations of the drug than others that also fall in the CQR category. In this review we investigate the evidence for and against the proposal that CQ kills parasites by generating oxidative stress. Further, we examine a long-held idea that the glutathione system of malaria parasites plays a role in CQ resistance. We conclude that there is strong evidence that glutathione levels modulate CQ response in the rodent malaria species Plasmodium berghei, but that a role for redox in contributing to the degree of CQ resistance in species infectious to humans has not been firmly established.
Keywords: Plasmodium; chloroquine resistance; glutathione; antioxidant defence
Rights: © 2011 Australian Society for Parasitology. Published by Elsevier Ltd. Open access under CC BY-NC-ND license.
RMID: 0020139346
DOI: 10.1016/j.ijpddr.2011.11.001
Grant ID: http://purl.org/au-research/grants/nhmrc/585519
http://purl.org/au-research/grants/nhmrc/418055
Appears in Collections:Molecular and Biomedical Science publications

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