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神经元单胺再摄取抑制剂增强了抗氯喹恶性疟原虫在体外对氯喹的敏感性。

Neuronal monoamine reuptake inhibitors enhance in vitro susceptibility to chloroquine in resistant Plasmodium falciparum.

作者信息

Coutaux A F, Mooney J J, Wirth D F

机构信息

Department of Tropical Public Health, Harvard School of Public Health, Boston, Massachusetts 02115.

出版信息

Antimicrob Agents Chemother. 1994 Jun;38(6):1419-21. doi: 10.1128/AAC.38.6.1419.

DOI:10.1128/AAC.38.6.1419
PMID:8092848
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC188223/
Abstract

Chloroquine resistance in Plasmodium falciparum was reversed in vitro by the neuronal monoamine reuptake inhibitors and antidepressants desipramine, sertraline, fluoxetine, and norfluoxetine but not by carbamazepine, an antiseizure and mood-stabilizing tricyclic drug resembling desipramine which only weakly inhibits neuronal monoamine reuptake. These findings have important clinical implications for drug combination therapy.

摘要

恶性疟原虫对氯喹的耐药性在体外可被神经元单胺再摄取抑制剂及抗抑郁药地昔帕明、舍曲林、氟西汀和去甲氟西汀逆转,但不能被卡马西平逆转,卡马西平是一种抗癫痫和稳定情绪的三环类药物,与地昔帕明相似,仅能微弱抑制神经元单胺再摄取。这些发现对联合药物治疗具有重要的临床意义。

相似文献

1
Neuronal monoamine reuptake inhibitors enhance in vitro susceptibility to chloroquine in resistant Plasmodium falciparum.神经元单胺再摄取抑制剂增强了抗氯喹恶性疟原虫在体外对氯喹的敏感性。
Antimicrob Agents Chemother. 1994 Jun;38(6):1419-21. doi: 10.1128/AAC.38.6.1419.
2
Role of the neurotransmitter reuptake-blocking activity of antidepressants in reversing chloroquine resistance in vitro in Plasmodium falciparum.抗抑郁药的神经递质再摄取阻断活性在体外逆转恶性疟原虫氯喹抗性中的作用。
Antimicrob Agents Chemother. 2000 Oct;44(10):2689-92. doi: 10.1128/AAC.44.10.2689-2692.2000.
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Reversal of chloroquine resistance with desipramine in isolates of Plasmodium falciparum from Central and West Africa.在来自中非和西非的恶性疟原虫分离株中,用去甲丙咪嗪逆转氯喹抗性。
Trans R Soc Trop Med Hyg. 1990 Jul-Aug;84(4):479-81. doi: 10.1016/0035-9203(90)90006-z.
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Desipramine reversal of chloroquine resistance in wild isolates of Plasmodium falciparum.去甲丙咪嗪逆转恶性疟原虫野生分离株对氯喹的耐药性。
Lancet. 1990 Jan 20;335(8682):164-5. doi: 10.1016/0140-6736(90)90034-3.
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Reversal of chloroquine resistance in malaria parasite Plasmodium falciparum by desipramine.地昔帕明逆转恶性疟原虫对氯喹的耐药性。
Science. 1988 Dec 2;242(4883):1301-3. doi: 10.1126/science.3057629.
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Enhancement of drug susceptibility in Plasmodium falciparum in vitro and Plasmodium berghei in vivo by mixed-function oxidase inhibitors.混合功能氧化酶抑制剂增强恶性疟原虫体外及伯氏疟原虫体内的药物敏感性
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Reversal of chloroquine resistance of 'wild' isolates of Plasmodium falciparum by desipramine.地昔帕明逆转恶性疟原虫“野生”分离株的氯喹抗性
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Role of the neurotransmitter reuptake-blocking activity of antidepressants in reversing chloroquine resistance in vitro in Plasmodium falciparum.抗抑郁药的神经递质再摄取阻断活性在体外逆转恶性疟原虫氯喹抗性中的作用。
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In vitro activity of nonsteroidal anti-inflammatory agents, phenotiazines, and antidepressants against Brucella species.非甾体抗炎药、吩噻嗪类药物及抗抑郁药对布鲁氏菌属的体外活性。
Eur J Clin Microbiol Infect Dis. 1996 May;15(5):418-20. doi: 10.1007/BF01690103.

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SOLUBILITY OF ACETYLENE IN LUNG TISSUE AS AN ERROR IN CARDIAC OUTPUT DETERMINATION WITH THE ACETYLENE METHOD.
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Trans R Soc Trop Med Hyg. 1990 Jul-Aug;84(4):479-81. doi: 10.1016/0035-9203(90)90006-z.
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Desipramine or cyproheptadine for reversing chloroquine resistance?用去甲丙咪嗪或赛庚啶逆转氯喹耐药性?
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Desipramine reversal of chloroquine resistance in wild isolates of Plasmodium falciparum.去甲丙咪嗪逆转恶性疟原虫野生分离株对氯喹的耐药性。
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