Abstract
Artemisinin is a natural product used as an alternative drug in the treatment of severe and multidrug-resistant malaria. In the present work we show that artemisinin shares with other sesquiterpene lactones the ability to inhibit the activation of the nuclear factor NF-kB: by this mechanism, artemisinin, as well as parthenolide, inhibits nitric oxide synthesis in cytokine-stimulated human astrocytoma T67 cells. These results suggest that artemisinin, in addition to its antiparasitic properties, could also exert a therapeutic effect on neurological complications of malaria.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Antimalarials / pharmacology*
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Artemisinins / pharmacology*
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Base Sequence
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Cell Line
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Cytokines / pharmacology
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DNA, Complementary / genetics
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Enzyme Inhibitors / pharmacology*
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Humans
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Lipopolysaccharides / pharmacology
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Mice
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NF-kappa B / antagonists & inhibitors
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NF-kappa B / metabolism*
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Neuroglia / drug effects
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Neuroglia / metabolism
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Nitric Oxide Synthase / antagonists & inhibitors*
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Nitric Oxide Synthase / genetics
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Nitric Oxide Synthase Type II
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Sesquiterpenes / pharmacology*
Substances
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Antimalarials
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Artemisinins
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Cytokines
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DNA, Complementary
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Enzyme Inhibitors
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Lipopolysaccharides
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NF-kappa B
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Sesquiterpenes
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parthenolide
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artemisinin
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NOS2 protein, human
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Nitric Oxide Synthase
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Nitric Oxide Synthase Type II
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Nos2 protein, mouse