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抗疟药青蒿素对恶性疟原虫体外阶段特异性配子体杀灭作用

Stage-specific gametocytocidal effect in vitro of the antimalaria drug qinghaosu on Plasmodium falciparum.

作者信息

Kumar N, Zheng H

机构信息

Department of Immunology and Infectious Diseases, Johns Hopkins University, School of Hygiene and Public Health, Baltimore, MD 21205.

出版信息

Parasitol Res. 1990;76(3):214-8. doi: 10.1007/BF00930817.

DOI:10.1007/BF00930817
PMID:2179946
Abstract

Qinghaosu, an anti-malaria drug, has been found to kill not only asexual blood stages but also the early stages of gametocytes of Plasmodium falciparum. The effect of qinghaosu in vitro depends on the concentration of the drug as well as on the initial parasitemia level (IC50 = 10-20 nM with 1% initial parasitemia). Resistance of P. falciparum to other anti-malaria drugs, e.g., chloroquine and pyrimethamine, did not affect susceptibility of its asexual and sexual stages to qinghaosu. Gametocytocidal effect of qinghaosu may play a role in the interruption of malaria transmission.

摘要

青蒿素是一种抗疟疾药物,已发现它不仅能杀死恶性疟原虫的无性血液阶段,还能杀死配子体的早期阶段。青蒿素在体外的作用取决于药物浓度以及初始寄生虫血症水平(初始寄生虫血症为1%时,IC50 = 10 - 20 nM)。恶性疟原虫对其他抗疟疾药物(如氯喹和乙胺嘧啶)的耐药性并不影响其无性和有性阶段对青蒿素的敏感性。青蒿素的杀配子体作用可能在疟疾传播阻断中发挥作用。

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本文引用的文献

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The effect of a single dose of primaquine on the gametocytes, gametogony and sporogony of Laverania falciparum.单剂量伯氨喹对恶性疟原虫配子体、配子生殖和孢子生殖的影响。
Bull World Health Organ. 1961;24(4-5):451-6.
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The treatment of Plasmodium falciparum infection with chloroquine, with a note on infectivity to mosquitoes of primaquine- and pyrimethamine-treated cases.用氯喹治疗恶性疟原虫感染,并附关于伯氨喹和乙胺嘧啶治疗病例对蚊子的感染性的说明。
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Complete in vitro maturation of Plasmodium falciparum gametocytes.
双氢青蒿素通过激活 Toll 信号通路抑制斯氏按蚊对约氏疟原虫的易感性。
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Whole genome sequencing identifies novel mutations in malaria parasites resistant to artesunate (ATN) and to ATN + mefloquine combination.全基因组测序鉴定出对青蒿琥酯(ATN)和 ATN + 甲氟喹联合用药具有抗药性的疟原虫的新突变。
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Parasite Epidemiol Control. 2023 Feb 17;21:e00292. doi: 10.1016/j.parepi.2023.e00292. eCollection 2023 May.
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Malar J. 2022 Nov 14;21(1):331. doi: 10.1186/s12936-022-04369-2.
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The Effect of Artemisinin-Based Drugs vs Non-artemisinin-based Drugs on Gametophyte Carrying in the Body After the Treatment of Uncomplicated Falciparum Malaria: A Systematic Review and Meta-analysis.青蒿素类药物与非青蒿素类药物对单纯性恶性疟治疗后体内携带配子体的影响:一项系统评价和荟萃分析。
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恶性疟原虫配子体的完全体外成熟
Nature. 1981 Nov 26;294(5839):364-6. doi: 10.1038/294364a0.
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Effects of qinghaosu and related compounds on incorporation of [G-3H] hypoxanthine by Plasmodium falciparum in vitro.青蒿素及相关化合物对恶性疟原虫体外摄取[G-3H]次黄嘌呤的影响。
Trans R Soc Trop Med Hyg. 1983;77(4):522-3. doi: 10.1016/0035-9203(83)90129-3.
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Biochem Pharmacol. 1983 Sep 1;32(17):2463-6. doi: 10.1016/0006-2952(83)90002-3.
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Lancet. 1984 Dec 15;2(8416):1360-1. doi: 10.1016/s0140-6736(84)92057-9.
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Gametocytocidal and sporontocidal effects of primaquine and of sulfadiazine with pyrimethamine in a chloroquine-resistant strain of Plasmodium falciparum.伯氨喹以及磺胺嘧啶与乙胺嘧啶联用对氯喹耐药恶性疟原虫株的配子体杀灭和子孢子抑制作用
Bull World Health Organ. 1968;38(4):625-32.
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The chemotherapy of rodent malaria, XXXIX. Ultrastructural changes following treatment with artemisinine of Plasmodium berghei infection in mice, with observations of the localization of [3H]-dihydroartemisinine in P. falciparum in vitro.啮齿动物疟疾的化学疗法,三十九。青蒿素治疗小鼠伯氏疟原虫感染后的超微结构变化,以及[3H] - 二氢青蒿素在体外恶性疟原虫中的定位观察。
Ann Trop Med Parasitol. 1985 Aug;79(4):367-74.
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