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本文引用的文献

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Imaging-based high-throughput screening assay to identify new molecules with transmission-blocking potential against Plasmodium falciparum female gamete formation.基于成像的高通量筛选试验,以鉴定对恶性疟原虫雌配子体形成具有传播阻断潜力的新分子。
Antimicrob Agents Chemother. 2015;59(6):3298-305. doi: 10.1128/AAC.04684-14. Epub 2015 Mar 23.
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A male and female gametocyte functional viability assay to identify biologically relevant malaria transmission-blocking drugs.一种用于鉴定具有生物学相关性的疟疾传播阻断药物的雌雄配子体功能活力测定法。
Antimicrob Agents Chemother. 2014 Dec;58(12):7292-302. doi: 10.1128/AAC.03666-14. Epub 2014 Sep 29.
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Gametocytocidal screen identifies novel chemical classes with Plasmodium falciparum transmission blocking activity.配子体杀灭筛选鉴定出具有恶性疟原虫传播阻断活性的新型化学类别。
PLoS One. 2014 Aug 26;9(8):e105817. doi: 10.1371/journal.pone.0105817. eCollection 2014.
4
Ethics, economics, and the use of primaquine to reduce falciparum malaria transmission in asymptomatic populations.伦理学、经济学以及使用伯氨喹减少无症状人群中恶性疟原虫传播的问题。
PLoS Med. 2014 Aug 19;11(8):e1001704. doi: 10.1371/journal.pmed.1001704. eCollection 2014 Aug.
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Primaquine or other 8-aminoquinoline for reducing P. falciparum transmission.伯氨喹或其他8-氨基喹啉用于减少恶性疟原虫传播。
Cochrane Database Syst Rev. 2014 Jun 30(6):CD008152. doi: 10.1002/14651858.CD008152.pub3.
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A flow cytometry-based quantitative drug sensitivity assay for all Plasmodium falciparum gametocyte stages.一种基于流式细胞术的针对所有恶性疟原虫配子体阶段的定量药物敏感性检测方法。
PLoS One. 2014 Apr 15;9(4):e93825. doi: 10.1371/journal.pone.0093825. eCollection 2014.
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Pharmacokinetic interactions between primaquine and chloroquine.伯氨喹与氯喹之间的药代动力学相互作用。
Antimicrob Agents Chemother. 2014 Jun;58(6):3354-9. doi: 10.1128/AAC.02794-13. Epub 2014 Mar 31.
8
Single dose primaquine for clearance of Plasmodium falciparum gametocytes in children with uncomplicated malaria in Uganda: a randomised, controlled, double-blind, dose-ranging trial.单次剂量磷酸萘酚喹清除乌干达无并发症疟疾儿童疟原虫配子体:一项随机、对照、双盲、剂量范围试验。
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9
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Cytostatic versus cytocidal profiling of quinoline drug combinations via modified fixed-ratio isobologram analysis.通过改良固定比例棋盘式分析研究喹啉类药物联合应用的细胞抑制与细胞杀伤作用。
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伯氨喹与裂殖体杀灭剂联合用药对恶性疟原虫无性血液期和配子体的体外活性

In Vitro Activities of Primaquine-Schizonticide Combinations on Asexual Blood Stages and Gametocytes of Plasmodium falciparum.

作者信息

Cabrera Mynthia, Cui Liwang

机构信息

Department of Entomology, The Pennsylvania State University, University Park, Pennsylvania, USA.

Department of Entomology, The Pennsylvania State University, University Park, Pennsylvania, USA

出版信息

Antimicrob Agents Chemother. 2015 Dec;59(12):7650-6. doi: 10.1128/AAC.01948-15. Epub 2015 Sep 28.

DOI:10.1128/AAC.01948-15
PMID:26416869
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4649191/
Abstract

Currently, the World Health Organization recommends addition of a 0.25-mg base/kg single dose of primaquine (PQ) to artemisinin combination therapies (ACTs) for Plasmodium falciparum malaria as a gametocytocidal agent for reducing transmission. Here, we investigated the potential interactions of PQ with the long-lasting components of the ACT drugs for eliminating the asexual blood stages and gametocytes of in vitro-cultured P. falciparum strains. Using the SYBR green I assay for asexual parasites and a flow cytometry-based assay for gametocytes, we determined the interactions of PQ with the schizonticides chloroquine, mefloquine, piperaquine, lumefantrine, and naphthoquine. With the sums of fractional inhibitory concentrations and isobolograms, we were able to determine mostly synergistic interactions for the various PQ and schizonticide combinations on the blood stages of P. falciparum laboratory strains. The synergism in inhibiting asexual stages and gametocytes was highly evident with PQ-naphthoquine, whereas synergism was moderate for the PQ-piperaquine, PQ-chloroquine, and PQ-mefloquine combinations. We have detected potentially antagonistic interactions between PQ and lumefantrine under certain drug combination ratios, suggesting that precautions might be needed when PQ is added as the gametocytocide to the artemether-lumefantrine ACT (Coartem).

摘要

目前,世界卫生组织建议在青蒿素联合疗法(ACTs)中添加单剂量0.25毫克碱基/千克的伯氨喹(PQ)用于治疗恶性疟原虫疟疾,作为一种杀配子剂以减少传播。在此,我们研究了PQ与ACT药物长效成分之间的潜在相互作用,这些成分用于清除体外培养的恶性疟原虫菌株的无性血液阶段和配子体。使用针对无性寄生虫的SYBR绿I检测法和针对配子体的基于流式细胞术的检测法,我们确定了PQ与裂殖体杀灭剂氯喹、甲氟喹、哌喹、蒿甲醚和萘喹之间的相互作用。通过部分抑制浓度总和及等效线图,我们能够确定各种PQ与裂殖体杀灭剂组合对恶性疟原虫实验室菌株血液阶段的相互作用大多为协同作用。PQ - 萘喹在抑制无性阶段和配子体方面的协同作用非常明显,而PQ - 哌喹、PQ - 氯喹和PQ - 甲氟喹组合的协同作用则为中等程度。我们在某些药物组合比例下检测到PQ与蒿甲醚之间存在潜在的拮抗相互作用,这表明当将PQ作为杀配子剂添加到蒿甲醚 - 蒿甲醚(科泰复)ACT中时可能需要谨慎。