黄芩素在烟曲霉菌性角膜炎中的抗炎作用
Anti-Inflammatory Effect of Baicalein in Aspergillus Fumigatus Keratitis
DOI: 10.12677/ACM.2020.1010342, PDF,  被引量   
作者: 朱玉楠, 朱筱嘉:青岛大学,山东 青岛;青岛大学附属医院,山东 青岛;彭旭东*:青岛大学附属医院,山东 青岛
关键词: 黄芩素烟曲霉菌性角膜炎抗炎Baicalein Aspergillus fumigatus Keratitis Anti-Inflammatory
摘要: 黄芩素(Baicalein, BE)是从双子叶唇形科植物黄芩(Scutellaria baicalensis)的干燥根中提取分离出来的一种黄酮类天然小分子化合物。研究发现黄芩素在感染性疾病中具有抗真菌,抗炎,抗氧化,调节机体免疫功能等作用。但在真菌性角膜炎中尚未有研究,本文就黄芩素在烟曲霉菌性小鼠角膜炎模型中的作用进行研究。方法:体外实验用烟曲霉菌感染HCECs后,再用黄芩素处理,PCR和ELISA评估IL-1β,TNF-α,IL-6的mRNA及蛋白的表达。体内实验用烟曲霉菌菌丝感染C57BL/6小鼠角膜制造烟曲霉菌角膜炎模型,再用黄芩素或DMSO处理,PCR和ELISA评估IL-1β,TNF-α,IL-6的mRNA及蛋白的表达。结果:黄芩素通过降低IL-1β,TNF-α,IL-6mRNA及蛋白减轻角膜炎的炎症反应。结论:黄芩素通过抑制促炎因子表达减轻小鼠角膜炎炎症反应。
Abstract: Baicalein (BE) is a natural small molecular compound of flavonoids extracted from the dried roots of Scutellaria baicalensis, a plant in the family of dicotyledons and labiatae. Studies have found that BE has anti-fungal, anti-inflammatory, anti-oxidant, and immune function regulation effects in infectious diseases. But it has not been studied in fungal keratitis. This article studies the role of BE in the mouse model of Aspergillus fumigatus (A. fumigatus) keratitis. Methods: In vitro experiments. After HCECs were infected with A. fumigatus, they were treated with BE, PCR and ELISA were used to evaluate the mRNA and protein expression of IL-1β, TNF-α, and IL-6. In vivo experiments, the cornea of C57BL/6 mice was infected with A. fumigatus hyphae to create an A. fumigatus keratitis model, and then it was treated with BE or DMSO. PCR and ELISA evaluated the mRNA and protein expression of IL-1β, TNF-α, IL-6. Results: BE reduced the inflammatory response of keratitis by reducing IL-1β, TNF-α, IL-6mRNA and protein. Conclusion: BE reduces the inflammatory response of mouse keratitis by inhibiting the expression of pro-inflammatory factors.
文章引用:朱玉楠, 朱筱嘉, 彭旭东. 黄芩素在烟曲霉菌性角膜炎中的抗炎作用[J]. 临床医学进展, 2020, 10(10): 2260-2269. https://doi.org/10.12677/ACM.2020.1010342

参考文献

[1] Bourcier, T., et al. (2017) Fungal Keratitis. Journal francais d’ophtalmologie, 40, e307-e313. [Google Scholar] [CrossRef] [PubMed]
[2] Garg, P., Roy, A. and Roy, S. (2016) Update on Fungal Keratitis. Current Opinion in Ophthalmology, 27, 333-339. [Google Scholar] [CrossRef
[3] Mahmoudi, S., et al. (2018) Fungal Keratitis: An Overview of Clinical and Laboratory Aspects. Mycoses, 61, 916-930. [Google Scholar] [CrossRef] [PubMed]
[4] Kredics, L., et al. (2015) Filamentous Fungal Infections of the Cornea: A Global Overview of Epidemiology and Drug Sensitivity. Mycoses, 58, 243-260. [Google Scholar] [CrossRef] [PubMed]
[5] Sahay, P., et al. (2019) Pharmacologic Therapy of Mycotic Keratitis. Survey of Ophthalmology, 64, 380-400. [Google Scholar] [CrossRef] [PubMed]
[6] Neoh, C., et al. (2014) Clinical Utility of Caspofungin Eye Drops in Fungal Keratitis. International Journal of Antimicrobial Agents, 44, 96-104. [Google Scholar] [CrossRef] [PubMed]
[7] Peng, L., et al. (2020) Therapeutic Effects of An Anti-IL-6 Antibody in Fungal Keratitis: Macrophage Inhibition and T Cell Subset Regulation. International Immunopharmacology, 85, Article ID: 106649. [Google Scholar] [CrossRef] [PubMed]
[8] Zhao, G., et al. (2017) The Role of Mincle in Innate Immune to Fungal Keratitis. Journal of Infection in Developing Countries, 11, 89-97. [Google Scholar] [CrossRef] [PubMed]
[9] Carnt, N., et al. (2012) Association of Single Nucleotide Polymorphisms of Interleukins-1β, -6, and -12B with Contact Lens Keratitis Susceptibility and Severity. Ophthalmology, 119, 1320-1327. [Google Scholar] [CrossRef] [PubMed]
[10] Gao, X., et al. (2016) LOX-1 and TLR4 Affect Each Other and Regulate the Generation of ROS in A. fumigatus Keratitis. International Immunopharmacology, 40, 392-399. [Google Scholar] [CrossRef] [PubMed]
[11] Yang, H., et al. (2020) Nerolidol Inhibits the LOX-1/IL-1β Signaling to Protect against the Aspergillus fumigatus Keratitis Inflammation Damage to the Cornea. International Immunopharmacology, 80, Article ID: 106118. [Google Scholar] [CrossRef] [PubMed]
[12] Yuan, K., et al. (2017) Dectin-1 Is Essential for IL-1β Production through JNK Activation and Apoptosis in Aspergillus fumigatus Keratitis. International Immunopharmacology, 52, 168-175. [Google Scholar] [CrossRef] [PubMed]
[13] Zhu, K., Mu, H. and Pi, B. (2016) Regulatory Effect of Caspase-11 on Interleukin-1β in the Fungal Keratitis. Pakistan Journal of Pharmaceutical Sciences, 29, 2327-2334.
[14] Che, C., et al. (2018) Wnt5a Contributes to Dectin-1 and LOX-1 Induced Host Inflammatory Response Signature in Aspergillus fumigatus Keratitis. Cellular Signalling, 52, 103-111. [Google Scholar] [CrossRef] [PubMed]
[15] Sun, Q., et al. (2019) Celastrol Ameliorates Aspergillus fumigatus Keratitis via Inhibiting LOX-1. International Immunopharmacology, 70, 101-109. [Google Scholar] [CrossRef] [PubMed]
[16] Zhan, L., et al. (2020) Honokiol Reduces Fungal Load, Toll-Like Receptor-2, and Inflammatory Cytokines in Aspergillus fumigatus Keratitis. Investigative Ophthalmology & Visual Science, 61, 48. [Google Scholar] [CrossRef] [PubMed]
[17] Zhou, Y., et al. (2019) The Role of Netrin-1 in the Mouse Cornea during Aspergillus fumigatus Infection. International Immunopharmacology, 71, 372-381. [Google Scholar] [CrossRef] [PubMed]
[18] Shen, J., et al. (2020) Traditional Uses, Clinical Studies, and Ten-Years Research Progress in Phytochemistry and Pharmacology of the Genus Scutellaria. Journal of Ethnopharmacology, 265, Article ID: 113198. [Google Scholar] [CrossRef] [PubMed]
[19] Fan, G., et al. (2013) Anti-Inflammatory Activity of Baicalein in LPS-Stimulated RAW264.7 Macrophages via Estrogen Receptor and NF-κB-Dependent Pathways. Inflammation, 36, 1584-1591. [Google Scholar] [CrossRef] [PubMed]
[20] Zhou, H., et al. (2018) Hepatoprotective Effect of Baicalein against Acetaminophen-Induced Acute Liver Injury in Mice. Molecules (Basel, Switzerland), 24, 131. [Google Scholar] [CrossRef] [PubMed]
[21] He, X., et al. (2015) Baicalein Attenuates Inflammatory Responses by Suppressing TLR4 Mediated NF-κB and MAPK Signaling Pathways in LPS-Induced Mastitis in Mice. International Immunopharmacology, 28, 470-476. [Google Scholar] [CrossRef] [PubMed]
[22] Wu, T., Wilhelmus, K. and Mitchell, B. (2003) Experimental Keratomycosis in a Mouse Model. Investigative Ophthalmology & Visual Science, 44, 210-216. [Google Scholar] [CrossRef] [PubMed]
[23] Wang, L., et al. (2015) Study of Pathogens of Fungal Keratitis and the Sensitivity of Pathogenic Fungi to Therapeutic Agents with the Disk Diffusion Method. Current Eye Research, 40, 1095-1101. [Google Scholar] [CrossRef] [PubMed]
[24] He, D., et al. (2016) Etiological Analysis of Fungal Keratitis and Rapid Identification of Predominant Fungal Pathogens. Mycopathologia, 181, 75-82. [Google Scholar] [CrossRef] [PubMed]
[25] Chen, P. and Xie, L. (2012) Signal Transduction Pathways Mediated by Toll-Like Receptors and Their Relations with Fungal Keratitis. Chinese Journal of Ophthalmology, 48, 80-84.
[26] Zhong, J., et al. (2016) Inhibition of TREM-1 and Dectin-1 Alleviates the Severity of Fungal Keratitis by Modulating Innate Immune Responses. PLoS ONE, 11, e0150114. [Google Scholar] [CrossRef] [PubMed]
[27] Keay, L., et al. (2011) Clinical and Microbiological Characteristics of Fungal Keratitis in the United States, 2001-2007: A Multicenter Study. Ophthalmology, 118, 920-926. [Google Scholar] [CrossRef] [PubMed]
[28] Dinda, B., et al. (2017) Therapeutic Potentials of Baicalin and Its Aglycone, Baicalein against Inflammatory Disorders. European Journal of Medicinal Chemistry, 131, 68-80. [Google Scholar] [CrossRef] [PubMed]
[29] Luo, J., et al. (2016) Baicalein Attenuates the Quorum Sensing-Controlled Virulence Factors of Pseudomonas aeruginosa and Relieves the Inflammatory Response in P. aeruginosa-Infected Macrophages by Downregulating the MAPK and NFκB Signal-Transduction Pathways. Drug Design, Development and Therapy, 10, 183-203. [Google Scholar] [CrossRef
[30] Sithisarn, P., et al. (2013) Differential Antiviral and Anti-Inflammatory Mechanisms of the Flavonoids Biochanin A and Baicalein in H5N1 Influenza A Virus-Infected Cells. Antiviral Research, 9, 41-48. [Google Scholar] [CrossRef] [PubMed]
[31] D’amico, R., et al. (2019) Effects of a New Compound Containing Palmitoylethanolamide and Baicalein in Myocardial Ischaemia/Reperfusion Injury in Vivo. Phytomedicine: International Journal of Phytotherapy and Phytopharmacology, 54, 27-42. [Google Scholar] [CrossRef] [PubMed]