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6-姜烯酚通过调节NLRP3炎性小体在新冠病毒相关炎症中表现出抗病毒和抗炎活性。

6-Shogaol Exhibits Anti-viral and Anti-inflammatory Activity in COVID-19-Associated Inflammation by Regulating NLRP3 Inflammasomes.

作者信息

Kode Jyoti, Maharana Jitendra, Dar Asif Amin, Mukherjee Shayanti, Gadewal Nikhil, Sigalapalli Dilep Kumar, Kumar Satyanshu, Panda Debashis, Ghosh Soumyajit, Keshry Supriya Suman, Mamidi Prabhudutta, Chattopadhyay Soma, Pradhan Trupti, Kailaje Vaishali, Inamdar Sunil, Gujjarwar Vidula

机构信息

Kode Lab, Tumor Immunology & Immunotherapy Group, Advanced Centre for Treatment, Research & Education in Cancer, Tata Memorial Centre, Kharghar, Navi Mumbai 410210, India.

Homi Bhabha National Institute (HBNI), Training School Complex, Anushakti Nagar, Mumbai 400094, India.

出版信息

ACS Omega. 2023 Jan 6;8(2):2618-2628. doi: 10.1021/acsomega.2c07138. eCollection 2023 Jan 17.

Abstract

Recent global health concern motivated the exploration of natural medicinal plant resources as an alternative target for treating COVID-19 infection and associated inflammation. In the current study, a phytochemical, 6-shogaol [1-(4-hydroxy-3-methoxyphenyl)dec-4-en-3-one; 6-SHO] was investigated as a potential anti-inflammatory and anti-COVID-19 agent. In virus release assay, 6-SHO efficiently (94.5%) inhibited SARS-CoV2 replication. When tested in the inflammasome activation model, 6-SHO displayed mechanistic action by regulating the expression of the inflammasome pathway molecules. In comparison to the existing drugs, remdesivir and hydroxy-chloroquine, 6-SHO was not only found to be as effective as the standard anti-viral drugs but also much superior and safe in terms of predicted physicochemical properties and clinical toxicity. Comparative molecular dynamics simulation demonstrated a stable interaction of 6-SHO with NLRP3 (the key inflammasome regulator) in the explicit water environment. Overall, this study provides important cues for further development of 6-SHO as potential anti-inflammatory and anti-viral therapeutic agents.

摘要

近期全球对健康的关注促使人们探索天然药用植物资源,将其作为治疗新冠病毒感染及相关炎症的替代靶点。在本研究中,一种植物化学物质6-姜烯酚[1-(4-羟基-3-甲氧基苯基)癸-4-烯-3-酮;6-SHO]被作为一种潜在的抗炎和抗新冠病毒药物进行研究。在病毒释放试验中,6-SHO有效(94.5%)抑制了新冠病毒的复制。在炎性小体激活模型中进行测试时,6-SHO通过调节炎性小体途径分子的表达发挥作用机制。与现有药物瑞德西韦和羟氯喹相比,6-SHO不仅被发现与标准抗病毒药物一样有效,而且在预测的理化性质和临床毒性方面更为优越和安全。比较分子动力学模拟表明,在明确的水环境中,6-SHO与NLRP3(关键的炎性小体调节因子)存在稳定的相互作用。总体而言,本研究为6-SHO作为潜在的抗炎和抗病毒治疗药物的进一步开发提供了重要线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c3f/9850479/67c62d1a0177/ao2c07138_0002.jpg

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