作者: Athip NILKAEO , Suthinee BHUVANATH , Sakonwun PRAPUTBUT , Seuptrakool WISESSOMBAT
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摘要: Chloroquine, quinine, artemisinin, and pyrimethamine are generally considered safe drugs for treatment of malaria during pregnancy; however, high doses these detrimental with adverse outcome pregnancy. Since antimalarial interaction placental cells has not been addressed, in this study, we employed a non-radioactive proliferation assay lactate dehydrogenase (LDH) release assays to investigate the effect on JAR trophoblastic cell survival. All drug resulted inhibition dose-dependent fashion (p < 0.05) IC50 at 6.96, 6.49, 6.69, 6.89 microg/mL chloroquine, artemisinin pyrimethamine, respectively. In addition, was accompanied by increased cytotoxicity. Analysis progression cycle showed that triggered G0/G1 S phase arrest. Furthermore, induced apoptotic death as visualized DNA fragmentation analysis techniques. Findings study revealed cytotoxicity human trophoblast is mediated both arrest induction could have important implications use treating