Sarcodonol A-D from fruiting bodies of Sarcodon imbricatus inhibits HCoV-OC43 induced apoptosis in MRC-5 cells

Bioorg Chem. 2023 Nov:140:106824. doi: 10.1016/j.bioorg.2023.106824. Epub 2023 Sep 1.

Abstract

Four new 26-carboxylated ergostane-type sterols (Sarcodonol A-D) were isolated from 70% ethanol extracts of dried fruiting bodies of Sarcodon imbricatus. Their chemical structures were elucidated using 1D- and 2D-nuclear magnetic resonance and high-resolution electrospray ionization mass spectrometry, and confirmed by comparison with previously reported data. As far as we know, this is the first instance of isolating a 26-carboxylated ergostane-type sterol from nature. The determined antiviral efficacy of sarcodonol A-D (1-4) against HCoV-OC43 in MRC-5 cells confirmed that sarcodonol D (4) had significant antiviral activity. Notably, sarcodonol D (4) potently blocked virus infection at low-micromolar concentration and showed high SI (IC50 = 2.26 μM; CC50 > 100 μM; SI > 44.2). In addition, this research shows that the antiviral effect of sarcodonol D (4) via reduced apoptosis increased by viral infection is through mitochondrial stress regulation. This suggests that sarcodonol D (4) is a potential candidate for use as an antiviral treatment.

Keywords: Apoptosis; Ergostane-type sterol; HCoV-OC43; Mitochondria stress; Sarcodon imbricatus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antiviral Agents* / chemistry
  • Antiviral Agents* / pharmacology
  • Apoptosis
  • Basidiomycota* / chemistry
  • Carboxylic Acids
  • Coronavirus OC43, Human*
  • Fruiting Bodies, Fungal / chemistry
  • Sterols* / chemistry
  • Sterols* / pharmacology

Substances

  • Antiviral Agents
  • Carboxylic Acids
  • Sterols

Supplementary concepts

  • Sarcodon imbricatus