壳聚糖对小鼠侵袭性念珠菌病的治疗作用

Amel M. Soliman, Sohair R. Fahmy, Wessam A. Mohamed
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引用次数: 12

摘要

抗生素耐药性的普遍存在导致需要开发新的方法来对抗以前容易治疗的感染。本研究旨在评价壳聚糖作为一种新的替代或补充抗真菌药物,单独或与两性霉素B联用对小鼠致病性白色念珠菌的抗真菌和抗氧化作用。80只中性粒细胞减少感染小鼠随机分为4组(每组20只)。第一组采用生理盐水、中性粒细胞减少感染(NI组)(IPC组,侵袭性肺念珠菌病)治疗,第二组采用壳聚糖(ED50)治疗(CE组),第三组采用两性霉素B (150 mg/kg)治疗(AMB组),第四组采用壳聚糖+两性霉素B治疗(CE + AMB组)。真菌接种后24 h开始处理,连续施用3天。所有先前的处理都显示出对白色念珠菌分离物的显著生长抑制,这是通过测量抑制带的平均直径来表明的。与IPC组相比,CE、AMB和AMB + CE处理的动物真菌负荷分别减少了73%、87%和90%。此外,与感染未治疗组相比,CE和/或AMB治疗24和72 h显著降低了肺组织中MDA、SOD、CAT和NO水平,并增加了GSH和。综上所述,CE治疗联合抗真菌治疗可减轻中性粒细胞减少小鼠IPC相关的氧化应激和肺损伤。
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Therapeutic efficacy of chitosan against invasive candidiasis in mice

The prevalence of antibiotic resistance has resulted in the need for new approaches to be developed to combat the previously easily treatable infections. This work aims to evaluate the antifungal and antioxidant effects of the chitosan, as a new alternative or complementary anti-fungal drug, alone or in combination with amphotericin B against a pathogenic Candida albicans in mice. Eighty neutropenic infected mice were randomly assigned into four main groups (20 mice/group). The 1st group was treated with saline, neutropenic infected (NI group) (IPC group, invasive pulmonary candidiasis), the 2nd group was treated with chitosan (ED50) (CE group), the 3rd group was treated with amphotericin B (150 mg/kg) (AMB group) and the 4th group was treated with chitosan plus amphotericin B (CE + AMB group). Treatment was started at 24 h after fungal inoculation and was administered for 3 consecutive days. All the previous treatments demonstrated notable growth inhibition against a C. albicans isolate as indicated by measuring the mean diameter of the inhibition zone. Compared with IPC group, CE, AMB, and AMB + CE-treated animals had 73%, 87%, and 90% reduction in fungal burden, respectively. Furthermore, treatment with CE and/or AMB for 24 and 72 h significantly decreased MDA, SOD, CAT and NO levels and increased GSH and in the lung tissues as compared with the infected untreated group. In conclusion, CE treatment, with the combination of antifungal therapy, can alleviate oxidative stress and lung injury associated with IPC in neutropenic mice.

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47 weeks
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