• 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

阿托伐他汀:与甲硝唑在体内联合作为抗治疗手段的协同作用。

Atorvastatin: In-Vivo Synergy with Metronidazole as Anti- Therapy.

作者信息

Basyoni Maha M A, Fouad Shawky A, Amer Marwa F, Amer Ahmed Fathy, Ismail Dalia Ibrahim

机构信息

Medical Parasitology Department, Faculty of Medicine, Cairo University, Egypt.

Internal Medicine Department, Faculty of Medicine, Cairo University, Egypt.

出版信息

Korean J Parasitol. 2018 Apr;56(2):105-112. doi: 10.3347/kjp.2018.56.2.105. Epub 2018 Apr 30.

DOI:10.3347/kjp.2018.56.2.105
PMID:29742864
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5976012/
Abstract

is an enteric Straminopile in tropical, subtropical and developing countries. Metronidazole has been a chemotheraputic for blastocystosis. Failures in its regimens were reported and necessitate new studies searching for alternative therapeutic agents. Aim of current study is to investigate potential effects of Atorvastatin (AVA) compared to the conventional chemotherapeutic MTZ in experimentally -infected mice. Anti- efficacy of AVA was evaluated parasitologically, histopathologically and by transmission electron microscopy using MTZ (10 mg/kg) as a control. Therapeutic efficacy of AVA was apparently dose-dependent. Regimens of AVA (20 and 40 mg/kg) proved effective against infections with high reduction in shedding (93.4-97.9%) compared to MTZ (79.3%). The highest reductions (98.1% and 99.4%) were recorded in groups of combination treatments AVA 20-40 mg/kg and MTZ 10 mg/kg. was nearly eradicated by the 20th day post infection. Genotype analysis revealed that genotype I was most susceptible, genotype III was less. Histopathologic and ultrastructural studies revealed apoptotic changes in and significant improvement of intestinal histopathological changes more remarkable in combinational therapy groups. Thus, the present study offers AVA as a potential candidate for therapy combined with MTZ.

摘要

是热带、亚热带和发展中国家的一种肠道茸鞭生物。甲硝唑一直是治疗芽囊原虫病的化疗药物。有报道称其治疗方案存在失败情况,因此需要开展新的研究来寻找替代治疗药物。本研究的目的是在实验感染小鼠中,将阿托伐他汀(AVA)与传统化疗药物甲硝唑(MTZ)进行比较,研究其潜在效果。以MTZ(10mg/kg)作为对照,通过寄生虫学、组织病理学以及透射电子显微镜观察来评估AVA的抗虫效果。AVA的治疗效果明显呈剂量依赖性。与MTZ(79.3%)相比,AVA(20和40mg/kg)方案对感染有效,虫体排出量大幅减少(93.4 - 97.9%)。AVA 20 - 40mg/kg与MTZ 10mg/kg联合治疗组的虫体减少率最高(分别为98.1%和99.4%)。感染后第20天虫体几乎被根除。基因型分析显示,I型基因型最敏感,III型较不敏感。组织病理学和超微结构研究显示,芽囊原虫出现凋亡变化,联合治疗组肠道组织病理学变化有显著改善。因此,本研究表明AVA有可能成为与MTZ联合治疗芽囊原虫病的候选药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd9/5976012/a41be53bdd88/kjp-56-2-105f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd9/5976012/b9e8cae821a1/kjp-56-2-105f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd9/5976012/be9941ca2d9d/kjp-56-2-105f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd9/5976012/a41be53bdd88/kjp-56-2-105f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd9/5976012/b9e8cae821a1/kjp-56-2-105f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd9/5976012/be9941ca2d9d/kjp-56-2-105f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd9/5976012/a41be53bdd88/kjp-56-2-105f3.jpg

相似文献

1
Atorvastatin: In-Vivo Synergy with Metronidazole as Anti- Therapy.阿托伐他汀:与甲硝唑在体内联合作为抗治疗手段的协同作用。
Korean J Parasitol. 2018 Apr;56(2):105-112. doi: 10.3347/kjp.2018.56.2.105. Epub 2018 Apr 30.
2
Apoptosis in Blastocystis spp. is related to subtype.囊胚型内阿米巴的细胞凋亡与亚型有关。
Trans R Soc Trop Med Hyg. 2012 Dec;106(12):725-30. doi: 10.1016/j.trstmh.2012.08.005. Epub 2012 Nov 8.
3
In Vitro Antimicrobial Susceptibility Patterns of Blastocystis.芽囊原虫的体外抗菌药敏模式
Antimicrob Agents Chemother. 2015 Aug;59(8):4417-23. doi: 10.1128/AAC.04832-14. Epub 2015 May 18.
4
Comparison of apoptotic responses in Blastocystis sp. upon treatment with Tongkat Ali and Metronidazole.比较东革阿里和甲硝唑对肠贾第鞭毛虫细胞凋亡反应的影响。
Sci Rep. 2021 Apr 9;11(1):7833. doi: 10.1038/s41598-021-81418-x.
5
In vitro toxicity evaluation of short cationic antimicrobial peptide (CM11) on Blastocystis sp.短阳离子抗菌肽 (CM11) 对芽囊原虫的体外毒性评价
Acta Trop. 2020 Apr;204:105384. doi: 10.1016/j.actatropica.2020.105384. Epub 2020 Feb 1.
6
Low efficacy of metronidazole in the eradication of Blastocystis hominis in symptomatic patients: Case series and systematic literature review.甲硝唑对有症状患者中溶组织内阿米巴的根除效果不佳:病例系列及系统文献综述
Gastroenterol Hepatol. 2017 Jun-Jul;40(6):381-387. doi: 10.1016/j.gastrohep.2016.11.003. Epub 2017 Mar 6.
7
Increase number of mitochondrion-like organelle in symptomatic Blastocystis subtype 3 due to metronidazole treatment.甲硝唑治疗导致有症状的芽囊原虫3型中线粒体样细胞器数量增加。
Parasitol Res. 2016 Jan;115(1):391-6. doi: 10.1007/s00436-015-4760-0. Epub 2015 Oct 20.
8
IN VIVO AND IN VITRO EFFICACY OF NIGELLA SATIVA AQUEOUS EXTRACT ON BLASTOCYSTIS HOMINIS.黑种草水提取物对人芽囊原虫的体内和体外疗效
J Egypt Soc Parasitol. 2016 Apr;46(1):27-34. doi: 10.12816/0026147.
9
IN VITRO ANTI-PROTOZOAL ACTIVITY OF PROPOLIS EXTRACT AND CYSTEINE PROTEASES INHIBITOR (PHENYL VINYL SULFONE) ON BLASTOCYSTIS SPECIES.蜂胶提取物和半胱氨酸蛋白酶抑制剂(苯乙烯砜)对芽囊原虫的体外抗寄生虫活性
J Egypt Soc Parasitol. 2016 Aug;46(2):261-272.
10
Treatment failure in patients with chronic Blastocystis infection.慢性芽囊原虫感染患者的治疗失败。
J Med Microbiol. 2014 Feb;63(Pt 2):252-257. doi: 10.1099/jmm.0.065508-0. Epub 2013 Nov 15.

引用本文的文献

1
Assessment of the Therapeutic Role of Allium tuncelianum Extract in Rats Infected with Blastocystis Subtype 3.葱提取物对感染3型芽囊原虫大鼠的治疗作用评估
Acta Parasitol. 2025 Sep 3;70(5):188. doi: 10.1007/s11686-025-01130-y.
2
The Role of spp. in the Etiology of Gastrointestinal and Autoimmune Diseases.某些物种在胃肠道疾病和自身免疫性疾病病因学中的作用。 (注:原文本中“spp.”表述有误,推测可能是“species”,这里按照纠正后的理解翻译。)
Pathogens. 2025 Mar 25;14(4):313. doi: 10.3390/pathogens14040313.
3
Assessment of Lactobacillus acidophilus (L. acidophilus) therapeutic and prophylactic role in rats experimentally infected with Blastocystis subtype 3 (ST3).

本文引用的文献

1
Statin-induced chronic cholesterol depletion inhibits Leishmania donovani infection: Relevance of optimum host membrane cholesterol.他汀类药物诱导的慢性胆固醇耗竭抑制杜氏利什曼原虫感染:最佳宿主膜胆固醇的相关性
Biochim Biophys Acta. 2016 Sep;1858(9):2088-2096. doi: 10.1016/j.bbamem.2016.06.010. Epub 2016 Jun 16.
2
Exploring Leishmania donovani 3-hydroxy-3-methylglutaryl coenzyme A reductase (HMGR) as a potential drug target by biochemical, biophysical and inhibition studies.通过生化、生物物理和抑制研究探索杜氏利什曼原虫 3-羟基-3-甲基戊二酰辅酶 A 还原酶(HMGR)作为潜在的药物靶点。
Microb Pathog. 2014 Jan;66:14-23. doi: 10.1016/j.micpath.2013.11.001. Epub 2013 Nov 14.
3
嗜酸乳杆菌(L. acidophilus)对实验性感染3型芽囊原虫(ST3)大鼠的治疗和预防作用评估。
Parasitol Res. 2025 Jan 23;124(1):11. doi: 10.1007/s00436-024-08444-2.
4
Impact of atorvastatin and mesenchymal stem cells combined with ivermectin on murine trichinellosis.阿托伐他汀和间充质干细胞联合伊维菌素对旋毛虫病小鼠的影响。
Parasitol Res. 2023 Dec 18;123(1):57. doi: 10.1007/s00436-023-08077-x.
5
Antibiotics and Lipid-Modifying Agents: Potential Drug-Drug Interactions and Their Clinical Implications.抗生素与调脂药物:潜在的药物相互作用及其临床意义。
Pharmacy (Basel). 2023 Aug 19;11(4):130. doi: 10.3390/pharmacy11040130.
6
Joining forces: Leveraging novel combination therapies to combat infections with eukaryotic pathogens.携手合作:利用新型联合疗法对抗真核病原体感染。
PLoS Pathog. 2020 Dec 31;16(12):e1009081. doi: 10.1371/journal.ppat.1009081. eCollection 2020 Dec.
7
Prenylquinones in Human Parasitic Protozoa: Biosynthesis, Physiological Functions, and Potential as Chemotherapeutic Targets.人体寄生虫原生动物中的prenylquinones:生物合成、生理功能以及作为化学治疗靶点的潜力。
Molecules. 2019 Oct 16;24(20):3721. doi: 10.3390/molecules24203721.
Toxoplasma gondii relies on both host and parasite isoprenoids and can be rendered sensitive to atorvastatin.
刚地弓形虫依赖于宿主和寄生虫异戊烯醇,并可能对阿托伐他汀敏感。
PLoS Pathog. 2013;9(10):e1003665. doi: 10.1371/journal.ppat.1003665. Epub 2013 Oct 17.
4
Drug repurposing screen reveals FDA-approved inhibitors of human HMG-CoA reductase and isoprenoid synthesis that block Cryptosporidium parvum growth.药物重定位筛选揭示了 FDA 批准的人 HMG-CoA 还原酶和异戊烯合成抑制剂可阻断微小隐孢子虫的生长。
Antimicrob Agents Chemother. 2013 Apr;57(4):1804-14. doi: 10.1128/AAC.02460-12. Epub 2013 Feb 4.
5
Variable geographic distribution of Blastocystis subtypes and its potential implications.不同地理区域 Blastocystis 亚型的分布差异及其潜在影响。
Acta Trop. 2013 Apr;126(1):11-8. doi: 10.1016/j.actatropica.2012.12.011. Epub 2013 Jan 3.
6
Statin pleiotropy prevents rho kinase-mediated intestinal epithelial barrier compromise induced by Blastocystis cysteine proteases.他汀类药物的多效性可防止由蓝氏贾第鞭毛虫半胱氨酸蛋白酶引起的 rho 激酶介导的肠道上皮屏障损伤。
Cell Microbiol. 2012 Sep;14(9):1474-84. doi: 10.1111/j.1462-5822.2012.01814.x. Epub 2012 May 31.
7
Antimalarial activity of potential inhibitors of Plasmodium falciparum lactate dehydrogenase enzyme selected by docking studies.抗疟原虫乳酸脱氢酶抑制剂的对接研究筛选及其抗疟活性。
PLoS One. 2011;6(7):e21237. doi: 10.1371/journal.pone.0021237. Epub 2011 Jul 14.
8
Efficacy of antiamebic drugs in a mouse model.抗阿米巴药物在小鼠模型中的疗效。
Am J Trop Med Hyg. 2011 Apr;84(4):581-6. doi: 10.4269/ajtmh.2011.10-0580.
9
Current Views on the Clinical Relevance of Blastocystis spp.当前对囊胚期孢子虫属的临床相关性的看法
Curr Infect Dis Rep. 2010 Jan;12(1):28-35. doi: 10.1007/s11908-009-0073-8.
10
A rapid, high-throughput viability assay for Blastocystis spp. reveals metronidazole resistance and extensive subtype-dependent variations in drug susceptibilities.一种快速、高通量的 Blastocystis spp. 生存力检测方法揭示了甲硝唑耐药性以及药物敏感性的广泛亚型依赖性差异。
Antimicrob Agents Chemother. 2011 Feb;55(2):637-48. doi: 10.1128/AAC.00900-10. Epub 2010 Nov 22.