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Antifungal Cytotoxic and Immunomodulatory Properties of Tea Tree Oil and Its Derivative Components: Potential Role in Management of Oral Candidosis in Cancer Patients

机译:茶树油及其衍生物的抗真菌细胞毒性和免疫调节特性:在癌症患者口腔念珠菌病管理中的潜在作用

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摘要

Candida albicans forms oral biofilms that cause disease and are difficult to treat with conventional antifungal agents. Tea tree oil (TTO) is a natural compound with reported antimicrobial and immunomodulatory activities. The aims of the study were to evaluate the antifungal efficacy of TTO and key derivatives against C. albicans biofilms, to assess the toxicological effects of TTO on a clinically relevant oral cell line, and to investigate its impact on inflammation. TTO and its derivatives were examined against 100 clinical strains of C. albicans. Planktonic minimum inhibitory concentrations (MICs) were determined using the CLSI M-27A broth microdilution method. Sessile MICs were determined using an XTT reduction assay. Inhibition, time-kill, and mode of action studies were performed. OKF6-TERT2 epithelial cells were used for cytotoxicity and cytokine expression assays. Planktonic C. albicans isolates were susceptible to TTO, terpinen-4-ol (T-4-ol), and α-terpineol, with an MIC50 of 0.5, 0.25, and 0.25%, respectively. These three compounds also displayed potent activity against the 69 biofilm-forming strains, of which T-4-ol and α-terpineol displayed rapid kill kinetics. For all three compounds, 1 × MIC50 effectively inhibited biofilm growth when C. albicans were treated at 0, 1, and 2 h post adhesion. By scanning electron microscopy analysis and PI uptake, TTO and derivative components were shown to be cell membrane active. TTO and T-4-ol were cytotoxic at 1 × MIC50, whereas at 0.5 × MIC50 T-4-ol displayed no significant toxicity. Transcript and protein analysis showed a reduction of IL-8 when treated with TTO and T-4-ol. These data provide further in vitro evidence that TTO and its derivative components, specifically T-4-ol, exhibit strong antimicrobial properties against fungal biofilms. T-4-ol has safety advantages over the complete essential oil and may be suitable for prophylaxis and treatment of established oropharyngeal candidosis. A clinical trial of T-4-ol is worthy of consideration.
机译:白色念珠菌会形成导致疾病的口腔生物膜,并且难以用常规的抗真菌剂进行治疗。茶树油(TTO)是一种天然化合物,具有抗菌和免疫调节活性。该研究的目的是评估TTO和关键衍生物对白色念珠菌生物膜的抗真菌功效,评估TTO对临床相关口腔细胞系的毒理作用,并研究其对炎症的影响。针对100种白色念珠菌临床菌株检查了TTO及其衍生物。使用CLSI M-27A肉汤微稀释法确定浮游生物的最小抑菌浓度(MIC)。使用XTT还原测定法测定无症状MIC。进行了抑制,时间杀伤和作用方式研究。 OKF6-TERT2上皮细胞用于细胞毒性和细胞因子表达测定。浮游生物白色念珠菌分离株易受TTO,萜品四醇(T-4-ol)和α-萜品醇的影响,MIC50分别为0.5、0.25和0.25%。这三种化合物还显示出对69种生物膜形成菌株的有效活性,其中T-4-ol和α-萜品醇显示出快速的杀灭动力学。对于所有三种化合物,当在粘附后0、1,和2 h处理白色念珠菌时,1×MIC50有效抑制生物膜生长。通过扫描电子显微镜分析和PI摄取,TTO和衍生物成分显示出细胞膜活性。 TTO和T-4-ol在1××MIC50时具有细胞毒性,而在0.5××MIC50时,T-4-ol没有明显的毒性。转录和蛋白质分析显示,当用TTO和T-4-ol处理时,IL-8减少。这些数据提供了进一步的体外证据,表明TTO及其衍生物成分,特别是T-4-ol对真菌生物膜表现出强大的抗菌性能。 T-4-ol较完整的精油具有安全性优势,并且可能适用于预防和治疗已建立的口咽念珠菌病。 T-4-ol的临床试验值得考虑。

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