In vivo antifungal activity of farnesol combined with antifungal drugs on oral mucosal candidiasis in mice

被引:5
作者
Li, Chengxi [1 ,2 ,3 ]
Xu, Zheng [2 ,3 ,4 ]
Liu, Siqi [2 ,3 ,4 ]
Huang, Rhyme [2 ,3 ,4 ]
Duan, Wei [2 ,3 ,4 ]
Wei, Xin [2 ,3 ,4 ]
机构
[1] Nanjing Med Univ, Suzhou Sci & Technol City Hosp, Suzhou, Peoples R China
[2] Nanjing Med Univ, Dept Stomatol Hosp, Surg Tooth & Pulp, Nanjing, Peoples R China
[3] Nanjing Med Univ, State Key Lab Oral Dis Res Jiangsu Prov, Nanjing, Peoples R China
[4] Jiangsu Prov Oral Translat Med Engn Res Ctr, Nanjing, Peoples R China
基金
中国国家自然科学基金;
关键词
farnesol; antifungal drugs; oral candidiasis; cytokines; mouse model; AMPHOTERICIN-B; BIOFILM FORMATION; MURINE MODEL; ALBICANS; FLUCONAZOLE; COMBINATION; CASPOFUNGIN; MICAFUNGIN; MECHANISMS; INFECTION;
D O I
10.1080/08927014.2021.1967938
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The antifungal resistence of oral candidiasis is a serious clinical issue. The in vivo efficacy of farnesol combined with antifungals for oral candidiasis remain unknow. The possible therapeuticeffects of a combination of farnesol and antifungal drugs and the regulation of inflammatorycytokines in murine oral candidiasis were investigated in this study. An experimental oral candidiasis model was constructed using ICR mice. Farnesol at 25 and 50 lM did not change IL-17,IFN-gamma and TNF-alpha production during oral candidiasis compared with that of the control infected mice. The co-applications of farnesol (50 lM) and nystatin, farnesol (4 lM, 8 lM) and itraconazole, farnesol (25, 50 lM), and fluconazole enhanced the therapeutic activity of the antifungalagents alone against oral candidiasis. The effective combinations reduced the number of colonyforming units (CFU) of Candida albicans isolated from the oral cavity and oral lesions onthe tongue.
引用
收藏
页码:818 / 829
页数:12
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