贝母提取物可抑制 A549 细胞中由 SARS-Cov-2 核苷酸诱导的炎症反应

Peeranut Winidmanokul, Suthida Panwong, A. Panya
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摘要

SARS-CoV-2 感染会通过释放细胞因子引发宿主免疫反应,细胞因子释放过多会导致严重的炎症和危及生命的并发症。为了降低细胞因子风暴带来的风险,需要采取替代方法。泰国传统草药提取物被公认为是安全有效的抗炎药物,可用于治疗各种疾病。因此,本研究旨在考察诃子、蝙蝠葛、大青叶和穿心莲乙醇提取物在减轻 A549 肺泡基底上皮细胞系炎症方面的抗炎作用。我们比较分析了四种提取物在降低 TNF-α 刺激 A549 细胞诱导的 COX-2 上调方面的抗炎功效。其中,T. bellirica 在降低 COX-2 水平方面的功效最高,达到 0.38 倍。此外,我们还验证了T. bellirica在减少炎症诱导的SARS-CoV-2核壳方面的抗炎特性。表达 SARS-CoV-2 核苷酸的慢病毒转导显示,促炎细胞因子和介质(包括 TNF-α、IL-8、CXCL-10 和 COX-2)的表达呈剂量依赖性增加。有趣的是,用亚致死剂量的 T. bellirica(30 和 60 μg/mL)处理后,COX-2 的表达分别显著减少了 30% 和 70%,TNF-α 减少了 46% 和 75%,IL-8 减少了 39% 和 48%,CXCL-10 减少了 46% 和 80%。这些发现证实了T. bellirica的强效抗炎作用,凸显了其作为一种新型治疗方法的潜力,可减轻SARS-CoV-2和相关疾病中细胞因子风暴的严重程度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Terminalia bellirica Extract Suppresses SARS-Cov-2 Nucleocapsid-Induced Inflammation in A549 Cells
SARS-CoV-2 infection triggers a host-immune response via cytokine release that, when excessive, leads to severe inflammation and life-threatening complications. To reduce the risks associated with cytokine storms, alternative approaches are needed. Traditional Thai herbal extracts are recognized for their potential as safe and effective anti-inflammatory agents against various diseases. Hence, this study aims to examine the anti-inflammatory effects of ethanolic extracts from Terminalia chebula, Terminalia bellirica, Phyllanthus emblica, and Andrographis paniculata in reducing inflammation in the A549 alveolar basal epithelial cell lines. We conducted a comparative analysis of the anti-inflammation efficacy of four extracts in reducing the COX-2 upregulation induced by TNF-α stimulation in A549 cells. Among them, T. bellirica exhibited the highest effectiveness in reducing COX-2 levels to 0.38-fold. Furthermore, we validated the anti-inflammation properties of T. bellirica in diminishing inflammation-induced SARS-CoV-2 nucleocapsid. Lentivirus transduction expressing SARS-CoV-2 nucleocapsid demonstrated a dose-dependent increase in the expression of pro-inflammatory cytokines and mediators including TNF-α, IL-8, CXCL-10, and COX-2. Interestingly, treatment with sublethal doses of T. bellirica (30 and 60 μg/mL) led to a significant reduction in COX-2 expression by 30% and 70%, TNF-α by 46% and 75%, IL-8 by 39% and 48%, and CXCL-10 by 46% and 80%, respectively. These findings confirm the potent anti-inflammatory effects of T. bellirica, highlighting its potential as a novel treatment for alleviating the severity of cytokine storms in SARS-CoV-2 and related diseases.
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