Publication | Closed Access
Reversal of Chloroquine Resistance in <i>Plasmodium falciparum</i> by Verapamil
558
Citations
20
References
1987
Year
Plasmodium falciparum, like neoplastic cells, develops resistance to multiple structurally unrelated drugs. The study investigates whether shared resistance mechanisms in P. falciparum and neoplastic cells allow reversal of resistance using the same pharmacological agents.
The parasite Plasmodium falciparum, like neoplastic cells, develops resistance to multiple structurally unrelated drugs. If the mechanisms by which P. falciparum and neoplastic cells become resistant are similar, then it may be possible to reverse the resistance in the two types of cells by the same pharmacological agents. Verapamil, a calcium channel blocker, completely reversed chloroquine resistance in two chloroquine-resistant P. falciparum clones from Southeast Asia and Brazil. Verapamil reversed chloroquine resistance at the same concentration (1 X 10(-6)M) as that at which it reversed resistance in multidrug-resistant cultured neoplastic cells. This same concentration of verapamil had no effect on chloroquine-sensitive parasites. Hence, chloroquine resistance in P. falciparum may fit the criteria for the multidrug-resistant phenotype.
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