Key Laboratory of Medicinal Chemistry for Natural Resource, Ministry of Education and Yunnan Province, School of Chemical Science and Technology, Yunnan University, Kunming, 650091, People's Republic of China.
Key Laboratory of Medicinal Chemistry for Natural Resource, Ministry of Education and Yunnan Province, School of Chemical Science and Technology, Yunnan University, Kunming, 650091, People's Republic of China.
J Ethnopharmacol. 2020 Oct 28;261:113119. doi: 10.1016/j.jep.2020.113119. Epub 2020 Jul 15.
As a traditional folk medicine, Acorus tatarinowii Schott was used to treat digestive diseases, such as diarrhea, which may be related to Candida albicans infection; however according to literature surveys, there have been few studies of A. tatarinowii focusing on its antimicrobial activity, and almost all describe investigations using crude extracts or fractions.
The aims of the current study were to isolate and identify antifungal fractions of A. tatarinowii based on their antifungal activity, explore the preliminary mechanism of 60% ethanol elution (AT60) by metabonomics, and evaluate the antifungal activity of AT60 in vivo and in vitro, to provide natural resources against fungal infections.
As a pilot evaluation of activity, A. tatarinowii fractions and compounds with antifungal bioactivity were isolated by bioactive-guided column chromatography, and identified by LC-QTOF-MS/MS and NMR spectroscopy. The antifungal effects of the active ingredients against resistant C. albicans were evaluated by in vivo and in vitro colony forming unit assays. The mechanism underlying the activity of AT60 against C. albicans was explored using an LC-QTOF-based metabonomics approach and fluorescence microscopy imaging.
AT60 showed better activity against C. albicans than the same dose of the first line antifungal drugs, fluconazole and itraconazole (positive control drugs). Subsequent phytochemical investigation of AT60 identified twenty-five known compounds, six of which were isolated: asaraldehyde (7), 1-(2,4,5-trimethoxyphenyl)-1,2-propanediol (12), α-asarone (14), β-asarone (15), γ-asarone (18), acotatarone C (19). Further, the compounds α-asarone (14) and acotatarone C (19) may be responsible for the antifungal activity, and exhibit synergistic effects. Metabonomics analysis indicated that AT60 can inhibit biofilm formation by regulating the C. albicans protein kinase C pathway.
Our results show that A. tatarinowii has potent bioactivity against C. albicans in vitro and in vivo, and can be considered an antifungal botanic agent.
作为一种传统民间药物,石菖蒲被用于治疗腹泻等消化系统疾病,这可能与白色念珠菌感染有关;然而,根据文献调查,关于菖蒲的抗菌活性研究甚少,几乎所有研究都描述了使用粗提物或馏分进行的研究。
本研究旨在基于其抗真菌活性分离和鉴定菖蒲的抗真菌馏分,通过代谢组学探讨 60%乙醇洗脱(AT60)的初步机制,并评估 AT60 在体内和体外的抗真菌活性,为抗真菌感染提供天然资源。
作为活性的初步评价,通过生物活性导向柱色谱法分离具有抗真菌生物活性的菖蒲馏分和化合物,并通过 LC-QTOF-MS/MS 和 NMR 光谱进行鉴定。通过体内和体外集落形成单位测定评估活性成分对耐药白色念珠菌的抗真菌作用。通过基于 LC-QTOF 的代谢组学方法和荧光显微镜成像探讨 AT60 对白色念珠菌活性的作用机制。
AT60 对白色念珠菌的活性优于氟康唑和伊曲康唑(阳性对照药物)等相同剂量的一线抗真菌药物。随后对 AT60 的植物化学研究鉴定了 25 种已知化合物,其中 6 种被分离出来:丁子香醛(7)、1-(2,4,5-三甲氧基苯基)-1,2-丙二醇(12)、α-细辛脑(14)、β-细辛脑(15)、γ-细辛脑(18)、菖蒲酮 C(19)。此外,化合物α-细辛脑(14)和菖蒲酮 C(19)可能是抗真菌活性的原因,并表现出协同作用。代谢组学分析表明,AT60 可以通过调节白色念珠菌蛋白激酶 C 途径抑制生物膜形成。
我们的研究结果表明,菖蒲对白色念珠菌具有较强的体外和体内抗活性,可作为一种抗真菌植物药。