• 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

卤代噻唑烷对实验感染免疫抑制沙鼠(黑线毛足鼠)体内微小隐孢子虫的活性。

Activity of halogeno-thiazolides against Cryptosporidium parvum in experimentally infected immunosuppressed gerbils (Meriones unguiculatus).

机构信息

Parasitology Department, Rouen University Hospital & EA 3800, University of Rouen, Rouen, France.

出版信息

Antimicrob Agents Chemother. 2013 Jun;57(6):2821-3. doi: 10.1128/AAC.01538-12. Epub 2013 Mar 11.

DOI:10.1128/AAC.01538-12
PMID:23478972
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3716183/
Abstract

Nitazoxanide and three halogeno-thiazolides, RM-4850, RM-4865, and RM-5038, were tested against Cryptosporidium parvum in experimentally infected immunosuppressed Mongolian gerbils. Daily 400-mg/kg doses of the four test drugs for 5 to 8 consecutive days produced similar reductions of oocyst shedding. Using early-infected gerbils, a shorter 4-day treatment with RM-5038 reduced oocyst shedding by 95%, compared to 47% for nitazoxanide (P = 0.02), suggesting that RM-5038 is more effective than nitazoxanide under the experimental conditions used.

摘要

硝唑尼特和三种卤代噻唑啉类化合物 RM-4850、RM-4865 和 RM-5038 对实验感染免疫抑制的蒙古沙鼠体内的微小隐孢子虫进行了测试。每日 400mg/kg 剂量的四种受试药物连续使用 5 至 8 天,可使卵囊脱落量相似减少。使用早期感染的沙鼠,用 RM-5038 进行更短的 4 天治疗,可使卵囊脱落减少 95%,而硝唑尼特为 47%(P=0.02),表明在使用的实验条件下,RM-5038 比硝唑尼特更有效。

相似文献

1
Activity of halogeno-thiazolides against Cryptosporidium parvum in experimentally infected immunosuppressed gerbils (Meriones unguiculatus).卤代噻唑烷对实验感染免疫抑制沙鼠(黑线毛足鼠)体内微小隐孢子虫的活性。
Antimicrob Agents Chemother. 2013 Jun;57(6):2821-3. doi: 10.1128/AAC.01538-12. Epub 2013 Mar 11.
2
Efficacy of nitazoxanide and paromomycin in biliary tract cryptosporidiosis in an immunosuppressed gerbil model.硝唑尼特和巴龙霉素在免疫抑制沙鼠模型中治疗胆道隐孢子虫病的疗效
J Antimicrob Chemother. 2006 Feb;57(2):353-5. doi: 10.1093/jac/dki456. Epub 2005 Dec 16.
3
Systemic efficacy on infection of aminoxanide (RM-5061), a new amino-acid ester thiazolide prodrug of tizoxanide.氨曲南(RM-5061),替硝唑新型氨基酸酯噻唑啉前药对感染的全身疗效。
Parasitology. 2021 Jul;148(8):975-984. doi: 10.1017/S0031182021000524. Epub 2021 Mar 29.
4
The immunomodulatory activity of secnidazole-nitazoxanide in a murine cryptosporidiosis model.硝唑尼特-那硝唑联合用药对隐孢子虫病模型鼠的免疫调节作用。
J Med Microbiol. 2021 Mar;70(3). doi: 10.1099/jmm.0.001327. Epub 2021 Feb 23.
5
Prophylactic and therapeutic efficacy of nitazoxanide against Cryptosporidium parvum in experimentally challenged neonatal calves.硝唑尼特对实验性感染新生犊牛隐孢子虫的预防和治疗效果。
Vet Parasitol. 2009 Mar 9;160(1-2):149-54. doi: 10.1016/j.vetpar.2008.10.094. Epub 2008 Nov 5.
6
Nitazoxanide.硝唑尼特
Indian Pediatr. 2005 Nov;42(11):1161-5.
7
Effects of pine bark extract administered to immunosuppressed adult mice infected with Cryptosporidium parvum.给予感染微小隐孢子虫的免疫抑制成年小鼠松树皮提取物的效果。
Am J Chin Med. 2001;29(3-4):469-75. doi: 10.1142/S0192415X01000484.
8
Assessment of Cryptosporidium parvum infection in immunocompetent and immunocompromised mice and its role in triggering intestinal dysplasia.评估免疫功能正常和免疫功能低下的小鼠中的微小隐孢子虫感染及其在引发肠道发育不良中的作用。
Int J Infect Dis. 2013 Aug;17(8):e593-600. doi: 10.1016/j.ijid.2012.11.023. Epub 2013 Jan 3.
9
Infectivity of Cryptosporidium hominis and Cryptosporidium parvum genotype 2 isolates in immunosuppressed Mongolian gerbils.人隐孢子虫和微小隐孢子虫2型分离株在免疫抑制蒙古沙鼠中的感染性。
Infect Immun. 2005 Aug;73(8):5252-5. doi: 10.1128/IAI.73.8.5252-5255.2005.
10
Efficacy of nitazoxanide against experimental cryptosporidiosis in goat neonates.硝唑尼特对新生山羊实验性隐孢子虫病的疗效。
Parasitol Res. 2007 Dec;102(1):163-6. doi: 10.1007/s00436-007-0744-z. Epub 2007 Sep 15.

引用本文的文献

1
and evaluation of the anti-cryptosporidial activity of eugenol.以及丁香酚抗隐孢子虫活性的评估。
Front Vet Sci. 2024 Mar 7;11:1374116. doi: 10.3389/fvets.2024.1374116. eCollection 2024.
2
Anti-Cryptosporidial Drug-Discovery Challenges and Existing Therapeutic Avenues: A "One-Health" Concern.抗隐孢子虫药物研发的挑战与现有治疗途径:一个“同一健康”问题
Life (Basel). 2024 Jan 3;14(1):80. doi: 10.3390/life14010080.
3
An update on biology and therapeutic avenues.生物学与治疗途径的最新进展。
J Parasit Dis. 2022 Sep;46(3):923-939. doi: 10.1007/s12639-022-01510-5. Epub 2022 Jun 22.
4
Assessment of chitosan nanoparticles in improving the efficacy of nitazoxanide on cryptosporidiosis in immunosuppressed and immunocompetent murine models.壳聚糖纳米颗粒对硝唑尼特治疗免疫抑制和免疫健全小鼠模型隐孢子虫病疗效的改善评估。
J Parasit Dis. 2021 Sep;45(3):606-619. doi: 10.1007/s12639-020-01337-y. Epub 2021 Jan 6.
5
Systemic efficacy on infection of aminoxanide (RM-5061), a new amino-acid ester thiazolide prodrug of tizoxanide.氨曲南(RM-5061),替硝唑新型氨基酸酯噻唑啉前药对感染的全身疗效。
Parasitology. 2021 Jul;148(8):975-984. doi: 10.1017/S0031182021000524. Epub 2021 Mar 29.
6
Comparative Pathobiology of the Intestinal Protozoan Parasites , , and .肠道原生动物寄生虫、和的比较病理生物学
Pathogens. 2019 Jul 29;8(3):116. doi: 10.3390/pathogens8030116.
7
Revisiting the global problem of cryptosporidiosis and recommendations.重新审视隐孢子虫病的全球问题及建议。
Trop Parasitol. 2017 Jan-Jun;7(1):8-17. doi: 10.4103/2229-5070.202290.
8
Nitazoxanide: a first-in-class broad-spectrum antiviral agent.硝唑尼特:一种一流的广谱抗病毒药物。
Antiviral Res. 2014 Oct;110:94-103. doi: 10.1016/j.antiviral.2014.07.014. Epub 2014 Aug 7.

本文引用的文献

1
Thiazolide-induced apoptosis in colorectal cancer cells is mediated via the Jun kinase-Bim axis and reveals glutathione-S-transferase P1 as Achilles' heel.噻唑烷酮诱导结直肠癌细胞凋亡是通过 Jun 激酶-Bim 轴介导的,并揭示谷胱甘肽 S-转移酶 P1 是阿喀琉斯之踵。
Oncogene. 2012 Sep 13;31(37):4095-106. doi: 10.1038/onc.2011.575. Epub 2011 Dec 12.
2
Evaluation of new thiazolide/thiadiazolide derivatives reveals nitro group-independent efficacy against in vitro development of Cryptosporidium parvum.评价新型噻唑烷/噻二唑烷衍生物对隐孢子虫体外发育的疗效,发现与硝基基团无关。
Antimicrob Agents Chemother. 2010 Mar;54(3):1315-8. doi: 10.1128/AAC.00614-09. Epub 2010 Jan 4.
3
In vitro efficacy of nitro- and halogeno-thiazolide/thiadiazolide derivatives against Sarcocystis neurona.硝基和卤代噻唑酯/噻二唑酯衍生物对犬新孢子虫的体外药效
Vet Parasitol. 2009 Jun 10;162(3-4):230-5. doi: 10.1016/j.vetpar.2009.03.022. Epub 2009 Mar 25.
4
Thiazolides inhibit growth and induce glutathione-S-transferase Pi (GSTP1)-dependent cell death in human colon cancer cells.噻唑类化合物可抑制人结肠癌细胞的生长,并诱导依赖谷胱甘肽-S-转移酶Pi(GSTP1)的细胞死亡。
Int J Cancer. 2008 Oct 15;123(8):1797-806. doi: 10.1002/ijc.23755.
5
Antiparasitic drug nitazoxanide inhibits the pyruvate oxidoreductases of Helicobacter pylori, selected anaerobic bacteria and parasites, and Campylobacter jejuni.抗寄生虫药物硝唑尼特可抑制幽门螺杆菌、某些厌氧菌和寄生虫以及空肠弯曲菌的丙酮酸氧化还原酶。
Antimicrob Agents Chemother. 2007 Mar;51(3):868-76. doi: 10.1128/AAC.01159-06. Epub 2006 Dec 11.
6
Activities of tizoxanide and nitazoxanide compared to those of five other thiazolides and three other agents against anaerobic species.与其他五种噻唑类化合物及其他三种药物相比,替唑尼特和硝唑尼特对厌氧菌的活性。
Antimicrob Agents Chemother. 2006 Mar;50(3):1112-7. doi: 10.1128/AAC.50.3.1112-1117.2006.
7
Identification of isoflavone derivatives as effective anticryptosporidial agents in vitro and in vivo.异黄酮衍生物作为体外和体内有效的抗隐孢子虫药物的鉴定。
J Med Chem. 2006 Feb 23;49(4):1450-4. doi: 10.1021/jm050973f.
8
Inhibitory activities of epidermal growth factor receptor tyrosine kinase-targeted dihydroxyisoflavone and trihydroxydeoxybenzoin derivatives on Sarcocystis neurona, Neospora caninum, and Cryptosporidium parvum development.表皮生长因子受体酪氨酸激酶靶向二羟基异黄酮和三羟基脱氧安息香衍生物对犬新孢子虫、犬小孢子虫和微小隐孢子虫发育的抑制活性。
Antimicrob Agents Chemother. 2005 Nov;49(11):4628-34. doi: 10.1128/AAC.49.11.4628-4634.2005.