• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

青蒿素和青蒿琥酯与调节氧化应激的药物联合对恶性疟原虫的抗疟作用。

The antimalarial action on Plasmodium falciparum of qinghaosu and artesunate in combination with agents which modulate oxidant stress.

作者信息

Krungkrai S R, Yuthavong Y

机构信息

Department of Biochemistry, Rajavithi Hospital, Bangkok, Thailand.

出版信息

Trans R Soc Trop Med Hyg. 1987;81(5):710-4. doi: 10.1016/0035-9203(87)90003-4.

DOI:10.1016/0035-9203(87)90003-4
PMID:3329778
Abstract

The antimalarial activity of qinghaosu (artemisinine) against Plasmodium falciparum in culture was enhanced by increased oxygen tension. Artesunate, a qinghaosu derivative, showed synergistic effects with miconazole, and with doxorubicin, both of which have been suggested to exert their chemotherapeutic effect through increasing the oxidant stress. In contrast, catalase, dithiothreitol and alpha-tocopherol reduced the effectiveness of qinghaosu in vitro. These results suggest that the action of qinghaosu and artesunate might involve increase in oxidant stress on the infected red cells.

摘要

青蒿素(青蒿琥酯)在体外培养中对恶性疟原虫的抗疟活性会因氧张力增加而增强。青蒿琥酯是青蒿素的衍生物,与咪康唑和阿霉素均呈现协同效应,这两种药物都被认为是通过增加氧化应激来发挥其化疗作用的。相比之下,过氧化氢酶、二硫苏糖醇和α-生育酚在体外会降低青蒿素的有效性。这些结果表明,青蒿素和青蒿琥酯的作用可能涉及增加被感染红细胞的氧化应激。

相似文献

1
The antimalarial action on Plasmodium falciparum of qinghaosu and artesunate in combination with agents which modulate oxidant stress.青蒿素和青蒿琥酯与调节氧化应激的药物联合对恶性疟原虫的抗疟作用。
Trans R Soc Trop Med Hyg. 1987;81(5):710-4. doi: 10.1016/0035-9203(87)90003-4.
2
Activated oxygen mediates the antimalarial activity of qinghaosu.活性氧介导青蒿素的抗疟活性。
Prog Clin Biol Res. 1989;313:95-104.
3
In vitro stage-specific sensitivity of Plasmodium falciparum to quinine and artemisinin drugs.恶性疟原虫对奎宁和青蒿素类药物的体外阶段特异性敏感性。
Int J Parasitol. 1996 May;26(5):519-25. doi: 10.1016/0020-7519(96)89380-5.
4
Qinghaosu-induced changes in the morphology of Plasmodium inui.青蒿素诱导的约氏疟原虫形态变化。
Am J Trop Med Hyg. 1985 May;34(3):424-8. doi: 10.4269/ajtmh.1985.34.424.
5
The effect of artesunate combined with standard antimalarials against chloroquine-sensitive and chloroquine-resistant strains of Plasmodium falciparum in vitro.青蒿琥酯联合标准抗疟药对恶性疟原虫氯喹敏感株和氯喹耐药株的体外作用。
Trans R Soc Trop Med Hyg. 1999 Jul-Aug;93(4):429-32. doi: 10.1016/s0035-9203(99)90147-5.
6
The effect of artemisinin combined with standard antimalarials against chloroquine-sensitive and chloroquine-resistant strains of Plasmodium falciparum in vitro.青蒿素联合标准抗疟药对恶性疟原虫氯喹敏感株和氯喹耐药株的体外作用。
J Trop Med Hyg. 1987 Feb;90(1):1-8.
7
Potentiation of the antimalarial activity of qinghaosu by methoxylated flavones.甲氧基黄酮对青蒿素抗疟活性的增强作用。
Trans R Soc Trop Med Hyg. 1987;81(3):434-6. doi: 10.1016/0035-9203(87)90161-1.
8
In-vitro tests on Philippine isolates of Plasmodium falciparum against four standard antimalarials and four qinghaosu derivatives.对菲律宾恶性疟原虫分离株针对四种标准抗疟药和四种青蒿素衍生物的体外试验。
Bull World Health Organ. 1994;72(5):729-35.
9
Stage-specific gametocytocidal effect in vitro of the antimalaria drug qinghaosu on Plasmodium falciparum.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
Parasitol Res. 1990;76(3):214-8. doi: 10.1007/BF00930817.
10
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.

引用本文的文献

1
GCN5 plays a key role in regulating artemisinin resistance-related stress responses.GCN5 在调控青蒿素耐药相关应激反应中发挥关键作用。
Antimicrob Agents Chemother. 2023 Oct 18;67(10):e0057723. doi: 10.1128/aac.00577-23. Epub 2023 Sep 13.
2
Blood-stage antiplasmodial activity and oocyst formation-blockage of metallo copper-cinchonine complex.金属铜-金鸡纳碱配合物的血期抗疟原虫活性和卵囊形成阻断作用。
Front Cell Infect Microbiol. 2022 Dec 1;12:1047269. doi: 10.3389/fcimb.2022.1047269. eCollection 2022.
3
Exploring the Role of Antioxidants to Combat Oxidative Stress in Malaria Parasites.
探讨抗氧化剂在对抗疟原虫氧化应激中的作用。
Curr Top Med Chem. 2022;22(24):2029-2044. doi: 10.2174/1568026622666220405121643.
4
In Vitro and In Silico Antimalarial Evaluation of FM-AZ, a New Artemisinin Derivative.新型青蒿素衍生物FM-AZ的体外和计算机模拟抗疟评估
Medicines (Basel). 2022 Jan 24;9(2):8. doi: 10.3390/medicines9020008.
5
Peroxide Antimalarial Drugs Target Redox Homeostasis in Infected Red Blood Cells.过氧化物抗疟药物靶向感染红细胞中的氧化还原稳态。
ACS Infect Dis. 2022 Jan 14;8(1):210-226. doi: 10.1021/acsinfecdis.1c00550. Epub 2022 Jan 5.
6
Antimalarial Natural Products.抗疟天然产物。
Prog Chem Org Nat Prod. 2022;117:1-106. doi: 10.1007/978-3-030-89873-1_1.
7
Plasmodium falciparum resistance to ACTs: Emergence, mechanisms, and outlook.恶性疟原虫对青蒿素类复方药物的抗药性:出现、机制和展望。
Int J Parasitol Drugs Drug Resist. 2021 Aug;16:102-118. doi: 10.1016/j.ijpddr.2021.05.007. Epub 2021 May 26.
8
Potential of Vitamin E Deficiency, Induced by Inhibition of α-Tocopherol Efflux, in Murine Malaria Infection.维生素 E 缺乏的潜力,由α-生育酚外排抑制引起,在鼠疟感染中。
Int J Mol Sci. 2018 Dec 24;20(1):64. doi: 10.3390/ijms20010064.
9
α-Tocopheryl succinate-suppressed development of cerebral malaria in mice.α-生育酚琥珀酸酯抑制小鼠脑型疟疾的发展。
Parasitol Res. 2018 Oct;117(10):3177-3182. doi: 10.1007/s00436-018-6016-2. Epub 2018 Jul 20.
10
Hydrogen peroxide dynamics in subcellular compartments of malaria parasites using genetically encoded redox probes.利用基因编码的氧化还原探针研究疟原虫亚细胞区室中的过氧化氢动力学。
Sci Rep. 2017 Sep 5;7(1):10449. doi: 10.1038/s41598-017-10093-8.