The antimalarial drug artemisinin alkylates heme in infected mice.
نویسندگان
چکیده
Heme alkylation by the antimalarial drug artemisinin is reported in vivo, within infected mice that have been treated at pharmacologically relevant doses. Adducts resulting from the alkylation of heme by the drug were characterized in the spleen of treated mice, and their glucuroconjugated derivatives were present in the urine. Because these heme-artemisinin adducts were not observed in noninfected mice, this report confirms that the alkylating activity of this antimalarial drug is related to the presence of the parasite in infected animals. The identification of heme-artemisinin adducts in mice should be considered as the signature of the alkylation capacity of artemisinin in vivo.
منابع مشابه
The antimalarial trioxaquine DU1301 alkylates heme in malaria-infected mice.
The in vivo alkylation of heme by the antimalarial trioxaquine DU1301 afforded covalent heme-drug adducts that were detected in the spleens of Plasmodium sp.-infected mice. This result indicates that the alkylation capacities of trioxaquines in mammals infected with Plasmodium strains are similar to that of artemisinin, a natural antimalarial trioxane-containing drug.
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18 The in vivo alkylation of heme by the antimalarial trioxaquine DU1301 afforded covalent 19 heme-drug adducts that have been detected in the spleen of malaria-infected mice. This result 20 indicates that the alkylation capacity of trioxaquines in mammals infected by Plasmodium is 21 similar to that of artemisinin, a natural antimalarial trioxane-containing drug. 22 AC CE PT ED Copyright © 200...
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ورودعنوان ژورنال:
- Proceedings of the National Academy of Sciences of the United States of America
دوره 102 38 شماره
صفحات -
تاریخ انتشار 2005