| Literature DB >> 33844528 |
Khanit Sa-Ngiamsuntorn1, Ampa Suksatu2, Yongyut Pewkliang3, Piyanoot Thongsri3, Phongthon Kanjanasirirat4, Suwimon Manopwisedjaroen2, Sitthivut Charoensutthivarakul4,5,6, Patompon Wongtrakoongate6,7, Supaporn Pitiporn8, Jarinya Chaopreecha2, Supasek Kongsomros2, Kedchin Jearawuttanakul4, Warawuth Wannalo4, Phisit Khemawoot9, Somchai Chutipongtanate9,10, Suparerk Borwornpinyo4,11, Arunee Thitithanyanont2, Suradej Hongeng4,10.
Abstract
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.Entities:
Year: 2021 PMID: 33844528 DOI: 10.1021/acs.jnatprod.0c01324
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050