穿心莲
穿心莲内酯
细胞毒性
细胞培养
IC50型
维罗细胞
病毒学
生物
传统医学
药理学
医学
病毒
体外
生物化学
病理
替代医学
遗传学
作者
Khanit Sa‐ngiamsuntorn,Ampa Suksatu,Yongyut Pewkliang,Piyanoot Thongsri,Phongthon Kanjanasirirat,Suwimon Manopwisedjaroen,Sitthivut Charoensutthivarakul,Patompon Wongtrakoongate,Supaporn Pitiporn,Jarinya Chaopreecha,Supasek Kongsomros,Kedchin Jearawuttanakul,Warawuth Wannalo,Phisit Khemawoot,Somchai Chutipongtanate,Suparerk Borwornpinyo,Arunee Thitithanyanont,Suradej Hongeng
标识
DOI:10.1021/acs.jnatprod.0c01324
摘要
The coronaviruses disease 2019 (COVID-19) caused by a novel coronavirus (SARS-CoV-2) has become a major health problem, affecting more than 50 million people with over one million deaths globally. Effective antivirals are still lacking. Here, we optimized a high-content imaging platform and the plaque assay for viral output study using the legitimate model of human lung epithelial cells, Calu-3, to determine the anti-SARS-CoV-2 activity of Andrographis paniculata extract and its major component, andrographolide. SARS-CoV-2 at 25TCID50 was able to reach the maximal infectivity of 95% in Calu-3 cells. Postinfection treatment of A. paniculata and andrographolide in SARS-CoV-2-infected Calu-3 cells significantly inhibited the production of infectious virions with an IC50 of 0.036 μg/mL and 0.034 μM, respectively, as determined by the plaque assay. The cytotoxicity profile developed over the cell line representatives of major organs, including liver (HepG2 and imHC), kidney (HK-2), intestine (Caco-2), lung (Calu-3), and brain (SH-SY5Y), showed a CC50 of >100 μg/mL for A. paniculata extract and 13.2-81.5 μM for andrographolide, respectively, corresponding to a selectivity index of over 380. In conclusion, this study provided experimental evidence in favor of A. paniculata and andrographolide for further development as a monotherapy or in combination with other effective drugs against SARS-CoV-2 infection.
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