American Journal of Tropical Medicine and Hygiene · 1993 · 43 citations · 0 references
MedicinePharmacologyPharmacotherapyAntimicrobial PharmacologyAntimicrobial ResistanceChemotherapyAntibacterial AgentsAntibacterial PharmacologyAntibiotic ResistanceAntimicrobial PharmacodynamicsCombination Antimicrobial TherapyEnzyme InhibitionAdditive EffectsAntimalarial AgentsAntimalarial ChemotherapyAntimalarial Drug CombinationsAntimalarial Drug DevelopmentChemotherapy Of MalariaIn Vivo StudiesTreatment Of Malaria
Several antibiotics that inhibit protein synthesis on 70S ribosomes, including the macrolide erythromycin, and the azalides azithromycin (ZITHROMAX) and CP-63,956, demonstrated antimalarial activity against two strains of Plasmodium berghei. In a four-day in vivo test, the azalides were 25-fold more potent than erythromycin against the chloroquine-sensitive P. berghei N strain, and displayed additive effects with chloroquine. This effect was not observed with the erythromycin-chloroquine combination. Against the chloroquine-resistant P. berghei MSU/RC strain, the azalides were 60-fold more potent than erythromycin. Additive effects were observed with azalide-chloroquine combinations against this strain, but these results were not significantly different from the erythromycin-chloroquine combination.