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概述了白杨素及其代谢产物黄芩苷抗 SARS-CoV-2 和抗炎的潜力:深入了解分子机制。

An overview of anti-SARS-CoV-2 and anti-inflammatory potential of baicalein and its metabolite baicalin: Insights into molecular mechanisms.

机构信息

Department of Chemistry, Tripura University, Suryamaninagar, Agartala, Tripura, India.

Department of Biochemistry and Molecular Genetics, University of Virginia, School of Medicine, Charlottesville, VA, USA.

出版信息

Eur J Med Chem. 2023 Oct 5;258:115629. doi: 10.1016/j.ejmech.2023.115629. Epub 2023 Jul 7.

Abstract

The current Coronavirus Disease 2019 (COVID-19) pandemic, caused by the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), is highly contagious infection that breaks the healthcare systems of several countries worldwide. Till to date, no effective antiviral drugs against COVID-19 infection have reached the market, and some repurposed drugs and vaccines are prescribed for the treatment and prevention of this disease. The currently prescribed COVID-19 vaccines are less effective against the newly emergent variants of concern of SARS-CoV-2 due to several mutations in viral spike protein and obviously there is an urgency to develop new antiviral drugs against this disease. In this review article, we systematically discussed the anti-SARS-CoV-2 and anti-inflammatory efficacy of two flavonoids, baicalein and its 7-O-glucuronide, baicalin, isolated from Scutellaria baicalensis, Oroxylum indicum, and other plants as well as their pharmacokinetics and oral bioavailability, for development of safe and effective drugs for COVID-19 treatment. Both baicalein and baicalin target the activities of viral S-, 3CL-, PL-, RdRp- and nsp13-proteins, and host mitochondrial OXPHOS for suppression of viral infection. Moreover, these compounds prevent sepsis-related inflammation and organ injury by modulation of host innate immune responses. Several nanoformulated and inclusion complexes of baicalein and baicalin have been reported to increase oral bioavailability, but their safety and efficacy in SARS-CoV-2-infected transgenic animals are not yet evaluated. Future studies on these compounds are required for use in clinical trials of COVID-19 patients.

摘要

当前由严重急性呼吸系统综合征冠状病毒 2 型(SARS-CoV-2)引起的 2019 年冠状病毒病(COVID-19)大流行是一种高度传染性的感染,使世界上许多国家的医疗保健系统不堪重负。迄今为止,尚无针对 COVID-19 感染的有效抗病毒药物上市,一些已批准用于治疗和预防这种疾病的药物和疫苗。由于病毒刺突蛋白的几个突变,目前规定用于 COVID-19 的疫苗对新出现的 SARS-CoV-2 关注变异体的效果较差,显然迫切需要开发针对这种疾病的新抗病毒药物。在这篇综述文章中,我们系统地讨论了从黄芩、黄桐和其他植物中分离得到的两种黄酮类化合物黄芩素及其 7-O-葡萄糖醛酸苷、黄芩苷的抗 SARS-CoV-2 和抗炎作用,以及它们的药代动力学和口服生物利用度,以开发用于 COVID-19 治疗的安全有效的药物。黄芩素和黄芩苷都靶向病毒的 S-、3CL-、PL-、RdRp-和 nsp13-蛋白以及宿主线粒体 OXPHOS 的活性,以抑制病毒感染。此外,这些化合物通过调节宿主固有免疫反应来预防与败血症相关的炎症和器官损伤。已经报道了几种纳米制剂和黄芩素和黄芩苷的包合物可以提高口服生物利用度,但它们在 SARS-CoV-2 感染的转基因动物中的安全性和疗效尚未得到评估。需要对这些化合物进行进一步研究,以用于 COVID-19 患者的临床试验。

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