Journal of Clinical Investigation · 1992 · 129 citations · 29 references
Life SciencesBiochemistryPharmacologyBiochemical PharmacologyMetabolismPharmacodynamicsAntiparasitic AgentsFatty Acid ChemistryFatty Acid MetabolismLipid MetabolismLipid PeroxidationMalariaAntimalarial AgentsAntimalarial ChemotherapyDocosahexaenoic AcidEicosapentaenoic AcidFatty AcidsMalaria AnemiaPlasmodium FalciparumTreatment Of Malaria
The polyunsaturated fatty acids docosahexaenoic acid (C22:6,n-3), eicosapentaenoic acid, arachidonic acid, and linoleic acid caused marked in vitro growth inhibition of Plasmodium falciparum, assessed by a radiometric assay. In contrast, negligible parasite killing was seen with oleic acid or docosanoic acid. Parasite killing was significantly increased when oxidized forms of polyunsaturated fatty acids were used. Antioxidants greatly reduced the fatty acid-induced killing. Mice infected with P. berghei and treated for 4 d with C22:6,n-3 showed marked reduction in parasitemia. The anemia associated with the infection was also alleviated by treatment with C22:6,n-3. The data provide new information that could be explored in order to develop new strategies in malaria treatment.
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Human Malaria Parasites in Continuous Culture
William Trager, James B. Jensen · Science · 1976 · 8K citations
Biochemistry of Plasmodium (malarial parasites).
I. W. Sherman · Microbiological Reviews · 1979 · 325 citations · Full text
Ian A. Clark, Nicholas H. Hunt, G.A. Butcher et al. · The Journal of Immunology · 1987 · 220 citations