• 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

1960年至1995年以及1999年至2004年期间从西非和中非分离出的布氏冈比亚锥虫菌株的体外药物敏感性比较。

Comparison of the in vitro drug sensitivity of Trypanosoma brucei gambiense strains from West and Central Africa isolated in the periods 1960-1995 and 1999-2004.

作者信息

Likeufack A C Lékané, Brun R, Fomena A, Truc P

机构信息

Organisation de Coordination pour la Lutte Contre les Endémies en Afrique Centrale, Yaoundé, Cameroon.

出版信息

Acta Trop. 2006 Nov;100(1-2):11-6. doi: 10.1016/j.actatropica.2006.09.003. Epub 2006 Oct 31.

DOI:10.1016/j.actatropica.2006.09.003
PMID:17078916
Abstract

The situation of human African trypanosomiasis remains serious with one of the main threats being the increasing number of relapses or treatment failures after melarsoprol treatment. In order to investigate and to compare drug sensitivities of trypanosomes isolated at different time periods and in different locations, two sets of Trypanosoma brucei gambiense strains were used. One set was isolated in the time period 1960-1981 and the other one in 1995-2004 from different locations of West and Central Africa. These isolates were not selected based on the treatment outcome but on availability. The drug sensitivity profile for all available drugs in use and the diamidine compound DB75 was established. IC(50) values were not significantly different between the "old" and "new" stocks. No indications for emerging drug resistance to any drug could be observed. The results indicate a relative stability of in vitro sensitivity of T. b. gambiense to trypanocidal drugs in space (West and Central Africa) and time (1960-2004).

摘要

人类非洲锥虫病的形势依然严峻,主要威胁之一是美拉胂醇治疗后复发或治疗失败的病例不断增加。为了调查和比较在不同时期和不同地点分离出的锥虫的药物敏感性,使用了两组布氏冈比亚锥虫菌株。一组于1960年至1981年期间分离,另一组于1995年至2004年期间从西非和中非的不同地点分离。这些分离株不是根据治疗结果而是根据可获得性选择的。确定了所有现有使用药物和二脒化合物DB75的药物敏感性概况。“旧”菌株和“新”菌株的半数抑制浓度(IC50)值没有显著差异。未观察到对任何药物出现耐药性的迹象。结果表明,布氏冈比亚锥虫在体外对杀锥虫药物的敏感性在空间(西非和中非)和时间(1960年至2004年)上具有相对稳定性。

相似文献

1
Comparison of the in vitro drug sensitivity of Trypanosoma brucei gambiense strains from West and Central Africa isolated in the periods 1960-1995 and 1999-2004.1960年至1995年以及1999年至2004年期间从西非和中非分离出的布氏冈比亚锥虫菌株的体外药物敏感性比较。
Acta Trop. 2006 Nov;100(1-2):11-6. doi: 10.1016/j.actatropica.2006.09.003. Epub 2006 Oct 31.
2
Genotypic and phenotypic characterization of Trypanosoma brucei gambiense isolates from Ibba, South Sudan, an area of high melarsoprol treatment failure rate.来自南苏丹伊巴地区的布氏冈比亚锥虫分离株的基因型和表型特征,该地区美拉胂醇治疗失败率很高。
Acta Trop. 2007 Nov-Dec;104(2-3):84-90. doi: 10.1016/j.actatropica.2007.07.007. Epub 2007 Aug 1.
3
Development of drug resistance in Trypanosoma brucei rhodesiense and Trypanosoma brucei gambiense. Treatment of human African trypanosomiasis with natural products (Review).罗德西亚布氏锥虫和冈比亚布氏锥虫耐药性的发展。天然产物治疗人类非洲锥虫病(综述)
Int J Mol Med. 2008 Oct;22(4):411-9.
4
Pharmacokinetics, Trypanosoma brucei gambiense efficacy, and time of drug action of DB829, a preclinical candidate for treatment of second-stage human African trypanosomiasis.DB829 的药代动力学、冈比亚锥虫疗效和药物作用时间,一种用于治疗第二期人类非洲锥虫病的临床前候选药物。
Antimicrob Agents Chemother. 2013 Nov;57(11):5330-43. doi: 10.1128/AAC.00398-13. Epub 2013 Aug 19.
5
The phenomenon of treatment failures in Human African Trypanosomiasis.人类非洲锥虫病治疗失败的现象
Trop Med Int Health. 2001 Nov;6(11):906-14. doi: 10.1046/j.1365-3156.2001.00775.x.
6
Melarsoprol sensitivity profile of Trypanosoma brucei gambiense isolates from cured and relapsed sleeping sickness patients from the Democratic Republic of the Congo.来自刚果民主共和国已治愈和复发昏睡病患者的布氏冈比亚锥虫分离株的美拉胂醇敏感性概况。
PLoS Negl Trop Dis. 2014 Oct 2;8(10):e3212. doi: 10.1371/journal.pntd.0003212. eCollection 2014 Oct.
7
Aquaporin 2 mutations in Trypanosoma brucei gambiense field isolates correlate with decreased susceptibility to pentamidine and melarsoprol.无鞭毛体利什曼原虫野毒株的水通道蛋白 2 突变与对喷他脒和米替福新的敏感性降低相关。
PLoS Negl Trop Dis. 2013 Oct 10;7(10):e2475. doi: 10.1371/journal.pntd.0002475. eCollection 2013.
8
Drug-resistance of Trypanosoma b. rhodesiense isolates from Tanzania.来自坦桑尼亚的罗德西亚布氏锥虫分离株的耐药性。
Trop Med Int Health. 2006 Feb;11(2):144-55. doi: 10.1111/j.1365-3156.2005.01545.x.
9
Innate lack of susceptibility of Ugandan Trypanosoma brucei rhodesiense to DL-alpha-difluoromethylornithine (DFMO).乌干达布氏罗得西亚锥虫对DL-α-二氟甲基鸟氨酸(DFMO)天然缺乏易感性。
Trop Med Parasitol. 1995 Sep;46(3):190-4.
10
[Melarsoprol].[美拉胂醇]
Med Trop (Mars). 1999;59(4):331-2.

引用本文的文献

1
Drug reformulation for a neglected disease. The NANOHAT project to develop a safer more effective sleeping sickness drug.针对被忽视疾病的药物重新配方。纳米帽项目旨在研发一种更安全、更有效的昏睡病药物。
PLoS Negl Trop Dis. 2021 Apr 15;15(4):e0009276. doi: 10.1371/journal.pntd.0009276. eCollection 2021 Apr.
2
Species-Specific Inactivation of Triosephosphate Isomerase from Trypanosoma brucei: Kinetic and Molecular Dynamics Studies.种属特异性的三磷酸甘油醛异构酶失活:动力学和分子动力学研究。
Molecules. 2017 Nov 24;22(12):2055. doi: 10.3390/molecules22122055.
3
Pentacyclic nitrofurans that rapidly kill nifurtimox-resistant trypanosomes.
能迅速杀死对硝呋替莫耐药的锥虫的五环硝基呋喃类药物。
J Antimicrob Chemother. 2016 Apr;71(4):956-63. doi: 10.1093/jac/dkv417. Epub 2015 Dec 18.
4
In vitro and in vivo evaluation of 28DAP010, a novel diamidine for treatment of second-stage African sleeping sickness.用于治疗第二阶段非洲昏睡病的新型双脒28DAP010的体外和体内评估。
Antimicrob Agents Chemother. 2014 Aug;58(8):4452-63. doi: 10.1128/AAC.02309-13. Epub 2014 May 27.
5
Aquaporin 2 mutations in Trypanosoma brucei gambiense field isolates correlate with decreased susceptibility to pentamidine and melarsoprol.无鞭毛体利什曼原虫野毒株的水通道蛋白 2 突变与对喷他脒和米替福新的敏感性降低相关。
PLoS Negl Trop Dis. 2013 Oct 10;7(10):e2475. doi: 10.1371/journal.pntd.0002475. eCollection 2013.
6
Pharmacokinetics and pharmacodynamics utilizing unbound target tissue exposure as part of a disposition-based rationale for lead optimization of benzoxaboroles in the treatment of Stage 2 Human African Trypanosomiasis.利用未结合的靶组织暴露作为基于处置的先导优化苯并硼杂环化合物治疗 2 期人类非洲锥虫病的理由的药代动力学和药效学。
Parasitology. 2014 Jan;141(1):104-18. doi: 10.1017/S003118201300098X. Epub 2013 Sep 5.
7
Pharmacokinetics, Trypanosoma brucei gambiense efficacy, and time of drug action of DB829, a preclinical candidate for treatment of second-stage human African trypanosomiasis.DB829 的药代动力学、冈比亚锥虫疗效和药物作用时间,一种用于治疗第二期人类非洲锥虫病的临床前候选药物。
Antimicrob Agents Chemother. 2013 Nov;57(11):5330-43. doi: 10.1128/AAC.00398-13. Epub 2013 Aug 19.
8
Isolation of Trypanosoma brucei gambiense from cured and relapsed sleeping sickness patients and adaptation to laboratory mice.从治愈和复发的昏睡病患者中分离冈比亚锥虫和适应实验室小鼠。
PLoS Negl Trop Dis. 2011 Apr 19;5(4):e1025. doi: 10.1371/journal.pntd.0001025.
9
Identification of a κ-opioid agonist as a potent and selective lead for drug development against human African trypanosomiasis.鉴定 κ-阿片样物质激动剂作为一种针对人类非洲锥虫病的药物开发的有效且选择性的先导化合物。
Biochem Pharmacol. 2010 Nov 15;80(10):1478-86. doi: 10.1016/j.bcp.2010.07.038. Epub 2010 Aug 7.
10
Cross-resistance to nitro drugs and implications for treatment of human African trypanosomiasis.对硝基药物的交叉耐药性及其对治疗非洲人类锥虫病的影响。
Antimicrob Agents Chemother. 2010 Jul;54(7):2893-900. doi: 10.1128/AAC.00332-10. Epub 2010 May 3.