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纳夫托金衍生物作为潜在的免疫调节剂:对COVID-19治疗的前景
Vitor Tassara Moraes1, Franco Jazon Caires1, Pedro V da Silva-Neto2
1Departamento de Ciências Biomoleculares, Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo-USP Ribeirão Preto 14040-903 SP Brazil gclososki@usp.br +55 16 3315-4208.
RSC advances
|February 23, 2024
概括
这项研究探讨了一种真菌纳夫托金,3,5,8-TMON及其衍生物的抗炎和抗病毒作用. 这些化合物显示出降低炎症标志物和抑制细胞培养中的SARS-CoV-2感染的潜力.
科学领域:
- 自然产品 化学 化学
- 免疫学 免疫学 免疫学
- 病毒学 病毒学
背景情况:
- 失调的炎症是严重的COVID-19结果的关键因素.
- 纳夫托基诺,如真菌中的3,5,8-TMON,显示出潜在的生物益处.
- 关于3,5,8-TMON的特性,特别是其抗炎和抗病毒作用的研究有限.
研究的目的:
- 评估3,5,8-TMON及其合成衍生物的抗炎和抗病毒作用.
- 研究它们对脂聚糖 (LPS) 诱导的炎症和SARS-CoV-2感染的影响.
- 探索对NF-kB,NO,IL-6和TNF等炎症标志物的度依赖性影响.
主要方法:
- 提取和酸性处理的真菌原始提取物 (科尔迪塞普斯种) 的提取. 为了获得3,5,8-TMON.
- 通过与氨酸反应合成两种新型衍生物 (3和4).
- 在体外细胞培养实验中,使用RAW 264.7,THP-1和Calu-3细胞进行了LPS或SARS-CoV-2的挑战.
主要成果:
- 原料提取物抑制了RAW 264.7细胞中LPS诱导的NF-kB,氧化 (NO) 和IL-6的产生.
- 3,5,8-TMON和衍生物3和4调节了THP-1细胞中的IL-6和TNF产生,以度依赖的方式.
- 在SARS-CoV-2感染期间,3,5,8-TMON显著降低了Calu-3细胞中的IL-6产生.
结论:
- 3,5,8-TMON及其衍生物具有有前途的抗炎和抗病毒特性.
- 这些化合物显示出治疗炎症和病毒感染的潜力,包括COVID-19.
- 进一步研究纳夫托基诺作为治疗剂是有必要的.
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