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硝酸益康唑与白屈菜红碱对白色念珠菌临床分离株的协同活性

Synergistic Activity of Econazole-Nitrate and Chelerythrine against Clinical Isolates of Candida albicans.

作者信息

Chen Zhibao, Li Xinran, Wu Xiuping, Wang Wei, Wang Wendong, Xin Mingxun, Shen Fengge, Liu Lihui, Liang Junchao, Li Lei, Yu Lu

机构信息

College of Life Science and Technology, Heilongjiang Bayi Agricultural University, Daqing, Heilongjiang 163319, China.

Key Laboratory of Zoonosis Research, Ministry of Education, Institute of Zoonosis, College of Animal Science and Veterinary Medicine, Jilin University, Changchun, China.

出版信息

Iran J Pharm Res. 2014 Spring;13(2):567-73.

PMID:25237352
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4157032/
Abstract

The aim of this investigation was to assess the in-vitro interaction of two antifungal agents, econazole-nitrate and chelerythrine, against ten fluconazole-resistant clinical isolates and one ATCC type strain 10231 of Candida albicans. The checkerboard microdilution method was performed according to the recommendations of the National Committee for Clinical Laboratory Standards, and the results were determined by visual examination. The interaction intensity was tested in all isolates using the fractional inhibitory concentration index (FICI). These experiments showed synergism between econazole-nitrate and chelerythrine in antifungal activity against C. albicans, and no antagonistic activity was observed in any of the strains tested. Moreover, time-kill curves were performed with selected strains to confirm the positive interactions. The similarity between the results of the FICI values and the time-kill curves revealed that chelerythrine greatly enhances the antifungal effects of econazole-nitrate against isolates of C. albicans. This synergistic effect may markedly reduce the dose of econazole-nitrate required to treat candidiasis, thereby decreasing the econazole-nitrate toxic side effects. This novel synergism might provide a potential combination treatment against fungal infections.

摘要

本研究的目的是评估两种抗真菌剂,即硝酸益康唑和白屈菜红碱,对10株耐氟康唑的白色念珠菌临床分离株和1株美国典型培养物保藏中心(ATCC)10231型白色念珠菌菌株的体外相互作用。棋盘微量稀释法是根据美国国家临床实验室标准委员会的建议进行的,结果通过目视检查确定。使用分数抑菌浓度指数(FICI)在所有分离株中测试相互作用强度。这些实验表明,硝酸益康唑和白屈菜红碱在抗白色念珠菌的抗真菌活性方面具有协同作用,在所测试的任何菌株中均未观察到拮抗活性。此外,对选定菌株进行了时间-杀菌曲线实验以确认阳性相互作用。FICI值结果与时间-杀菌曲线之间的相似性表明,白屈菜红碱可大大增强硝酸益康唑对白色念珠菌分离株的抗真菌作用。这种协同作用可能会显著降低治疗念珠菌病所需的硝酸益康唑剂量,从而减少硝酸益康唑的毒副作用。这种新型协同作用可能为真菌感染提供一种潜在的联合治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/732f/4157032/edae4a2680e5/ijpr-13-567-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/732f/4157032/64a80a37b544/ijpr-13-567-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/732f/4157032/edae4a2680e5/ijpr-13-567-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/732f/4157032/64a80a37b544/ijpr-13-567-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/732f/4157032/edae4a2680e5/ijpr-13-567-g002.jpg

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本文引用的文献

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Toxicol In Vitro. 2011 Dec;25(8):1581-7. doi: 10.1016/j.tiv.2011.05.028. Epub 2011 Jun 2.
2
In vitro interaction between fluconazole and triclosan against clinical isolates of fluconazole-resistant Candida albicans determined by different methods.不同方法测定氟康唑与三氯生体外抗氟康唑耐药白念珠菌临床分离株的相互作用。
Antimicrob Agents Chemother. 2011 Jul;55(7):3609-12. doi: 10.1128/AAC.01313-10. Epub 2011 May 16.
3
Combination immunotherapy of MAb B6.1 with fluconazole augments therapeutic effect to disseminated candidiasis.
单抗 B6.1 联合氟康唑免疫治疗增强播散性念珠菌病的疗效。
Arch Pharm Res. 2011 Mar;34(3):399-405. doi: 10.1007/s12272-011-0307-9. Epub 2011 May 6.
4
Structural modification of sanguinarine and chelerythrine and their antibacterial activity.血根碱和白屈菜红碱的结构修饰及其抗菌活性。
Nat Prod Res. 2011 May;25(9):863-75. doi: 10.1080/14786419.2010.482055.
5
Comparative evaluation of synergy of combinations of beta-lactams with fluoroquinolones or a macrolide in Streptococcus pneumoniae.比较评估β-内酰胺类与氟喹诺酮类或大环内酯类药物联合使用对肺炎链球菌的协同作用。
J Antimicrob Chemother. 2011 Apr;66(4):845-9. doi: 10.1093/jac/dkr016. Epub 2011 Feb 3.
6
Effects of the PKC inhibitors chelerythrine and bisindolylmaleimide I (GF 109203X) on delayed rectifier K+ currents.蛋白激酶 C 抑制剂白屈菜红碱和双吲哚马来酰亚胺 I(GF109203X)对延迟整流钾电流的影响。
Naunyn Schmiedebergs Arch Pharmacol. 2011 Feb;383(2):141-8. doi: 10.1007/s00210-010-0584-8. Epub 2010 Dec 1.
7
PKC signaling regulates drug resistance of the fungal pathogen Candida albicans via circuitry comprised of Mkc1, calcineurin, and Hsp90.PKC 信号通过由 Mkc1、钙调神经磷酸酶和 Hsp90 组成的电路调节真菌病原体白念珠菌的耐药性。
PLoS Pathog. 2010 Aug 26;6(8):e1001069. doi: 10.1371/journal.ppat.1001069.
8
Econazole nitrate-loaded MCM-41 for an antifungal topical powder formulation.载硝酸益康唑的 MCM-41 用于抗真菌局部粉体制剂。
J Pharm Sci. 2010 Nov;99(11):4738-45. doi: 10.1002/jps.22183.
9
Potent antifungal activity of extracts and pure compound isolated from pomegranate peels and synergism with fluconazole against Candida albicans.石榴皮提取物和纯化合物具有很强的抗真菌活性,并与氟康唑对白色念珠菌表现出协同作用。
Res Microbiol. 2010 Sep;161(7):534-40. doi: 10.1016/j.resmic.2010.05.002. Epub 2010 Jun 10.
10
New azoles with potent antifungal activity: design, synthesis and molecular docking.具有强效抗真菌活性的新型唑类化合物:设计、合成与分子对接
Eur J Med Chem. 2009 Oct;44(10):4218-26. doi: 10.1016/j.ejmech.2009.05.018. Epub 2009 May 24.