Protective Effect of Flavonoids from Ohwia caudata against Influenza a Virus Infection

  • Molecules. 2020 Sep 24;25(19):4387. doi: 10.3390/molecules25194387.
Eun Bin Kwon  1 Hye Jin Yang  1 Jang-Gi Choi  1 Wei Li  1
Affiliations
  • 1. Korean Medicine (KM) Application Center, Korea Institute of Oriental Medicine, Daegu 41062, Korea.
Abstract

To identify new potential anti-influenza compounds, we isolated six Flavonoids, 2'-hydroxyl yokovanol (1), 2'-hydroxyl neophellamuretin (2), yokovanol (3), swertisin (4), spinosin (5), and 7-methyl-apigenin-6-C-β-glucopyranosyl 2″-O-β-d-xylopyranoside (6) from MeOH extractions of Ohwia caudata. We screened these compounds for Antiviral activity using green fluorescent protein (GFP)-expressing H1N1 (A/PR/8/34) influenza A-infected RAW 264.7 cells. Compounds 1 and 3 exhibited significant inhibitory effects against influenza A viral Infection in co-treatment conditions. In addition, compounds 1 and 3 reduced viral protein levels, including M1, M2, HA, and neuraminidase (NA), and suppressed neuraminidase (NA) activity in RAW 264.7 cells. These findings demonstrated that 2'-hydroxyl yokovanol and yokovanol, isolated from O. caudate, inhibit influenza A virus by suppressing NA activity. The moderate inhibitory activities of these Flavonoids against influenza A virus suggest that they may be developed as novel anti-influenza drugs in the future.

Keywords
Ohwia caudata; flavonoid; influenza A; neuraminidase.
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