Cell Reports · 2022 · 34 citations · 49 references
Life SciencesBiochemistryPharmacologyEnzymologyLipid BiochemistryRedox BiochemistryAntioxidant DefenseEnzyme InhibitionLipid PeroxidationMalariaPeroxiredoxin BiologyRedox EnzymesAntimalarial AgentsAntimalarial Drug DevelopmentArtemisinin ResistanceMalaria ParasitesMalaria ResistancePhospholipase A2 InhibitionPhospholipase A2 PathwayPlasmodium Falciparum
inhibitor, Darapladib, increases lipid-peroxidation damage in the parasite and disrupts transport of hemoglobin-containing vesicles to the food vacuole, causing parasite death. Furthermore, inhibition of PRDX6 synergistically reduces the survival of artemisinin-resistant parasites following co-treatment of parasite cultures with artemisinin and Darapladib. Thus, PRDX6 is a host-derived drug target for development of antimalarial drugs that could help overcome artemisinin resistance.
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