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Scutellaria barbata D. Don Inhibits the Main Proteases (Mpro and TMPRSS2) of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection.
Huang, Sheng-Teng; Chen, Yeh; Chang, Wei-Chao; Chen, Hsiao-Fan; Lai, Hsiang-Chun; Lin, Yu-Chun; Wang, Wei-Jan; Wang, Yu-Chuan; Yang, Chia-Shin; Wang, Shao-Chun; Hung, Mien-Chie.
  • Huang ST; School of Chinese Medicine, China Medical University, Taichung 40402, Taiwan.
  • Chen Y; Department of Chinese Medicine, China Medical University Hospital, Taichung 40402, Taiwan.
  • Chang WC; Research Cancer Center for Traditional Chinese Medicine, Department of Medical Research, China Medical University Hospital, Taichung 40402, Taiwan.
  • Chen HF; An-Nan Hospital, China Medical University, Tainan 709, Taiwan.
  • Lai HC; Research Center for Cancer Biology, China Medical University, Taichung 40402, Taiwan.
  • Lin YC; New Drug Development Center, China Medical University, Taichung 40402, Taiwan.
  • Wang WJ; Graduate Institute of New Drug Development, China Medical University, Taichung 40402, Taiwan.
  • Wang YC; Center for Molecular Medicine, China Medical University Hospital, Taichung 40402, Taiwan.
  • Yang CS; Research Center for Cancer Biology, China Medical University, Taichung 40402, Taiwan.
  • Wang SC; New Drug Development Center, China Medical University, Taichung 40402, Taiwan.
  • Hung MC; Department of Chinese Medicine, China Medical University Hospital, Taichung 40402, Taiwan.
Viruses ; 13(5)2021 05 02.
Article in English | MEDLINE | ID: covidwho-1224250
ABSTRACT
In late 2019, the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic emerged to severely impact the global population, creating an unprecedented need for effective treatments. This study aims to investigate the potential of Scutellaria barbata D. Don (SB) as a treatment for SARS-CoV-2 infection through the inhibition of the proteases playing important functions in the infection by SARS-CoV-2. FRET assay was applied to investigate the inhibitory effects of SB on the two proteases involved in SARS-CoV-2 infection, Mpro and TMPRSS2. Additionally, to measure the potential effectiveness of SB treatment on infection inhibition, cellular models based on the Calu3 and VeroE6 cells and their TMPRSS2- expressing derivatives were assessed by viral pseudoparticles (Vpp) infection assays. The experimental approaches were conjugated with LC/MS analyses of the aqueous extracts of SB to identify the major constituent compounds, followed by a literature review to determine the potential active components of the inhibitory effects on protease activities. Our results showed that SB extracts inhibited the enzyme activities of Mpro and TMPRSS2. Furthermore, SB extracts effectively inhibited SARS-CoV-2 Vpp infection through a TMPRSS2-dependent mechanism. The aqueous extract analysis identified six major constituent compounds present in SB. Some of them have been known associated with inhibitory activities of TMPRSS2 or Mpro. Thus, SB may effectively prevent SARS-CoV-2 infection and replication through inhibiting Mpro and TMPRSS2 protease activities.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Serine Endopeptidases / Plant Extracts / Coronavirus 3C Proteases / COVID-19 Drug Treatment Type of study: Reviews Limits: Animals / Humans Language: English Year: 2021 Document Type: Article Affiliation country: V13050826

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Serine Endopeptidases / Plant Extracts / Coronavirus 3C Proteases / COVID-19 Drug Treatment Type of study: Reviews Limits: Animals / Humans Language: English Year: 2021 Document Type: Article Affiliation country: V13050826