Structural Characterization and Anti-Inflammatory Effects of 24-Methylcholesta-5(6), 22-Diene-3β-ol from the Cultured Marine Diatom Phaeodactylum tricornutum; Attenuate Inflammatory Signaling Pathways

Mar Drugs. 2023 Apr 3;21(4):231. doi: 10.3390/md21040231.

Abstract

In the present investigation, 24-methylcholesta-5(6), 22-diene-3β-ol (MCDO), a major phytosterol was isolated from the cultured marine diatom, Phaeodactylum tricornutum Bohlin, and in vitro and in vivo anti-inflammatory effects were determined. MCDO demonstrated very potent dose-dependent inhibitory effects on the production of nitric oxide (NO) and prostaglandin E2 (PGE2) against lipopolysaccharide (LPS)-induced RAW 264.7 cells with minimal cytotoxic effects. MCDO also demonstrated a strong and significant suppression of pro-inflammatory cytokines of interleukin-1β (IL-1β) production, but no substantial inhibitory effects were observed on the production of cytokines, including tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6) at the tested concentrations against LPS treatment on RAW macrophages. Western blot assay confirmed the suppression of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) protein expressions against LPS-stimulated RAW 264.7 cells. In addition, MCDO was assessed for in vivo anti-inflammatory effects using the zebrafish model. MCDO acted as a potent inhibitor for reactive oxygen species (ROS) and NO levels with a protective effect against the oxidative stress induced by LPS in inflammatory zebrafish embryos. Collectively, MCDO isolated from the cultured marine diatom P. tricornutum exhibited profound anti-inflammatory effects both in vitro and in vivo, suggesting that this major sterol might be a potential treatment for inflammatory diseases.

Keywords: Phaeodactylum tricornutum; anti-inflammatory effects; cultured marine diatom; zebrafish.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / pharmacology
  • Cyclooxygenase 2 / metabolism
  • Cytokines / metabolism
  • Diatoms* / metabolism
  • Interleukin-6 / metabolism
  • Lipopolysaccharides / pharmacology
  • NF-kappa B / metabolism
  • Nitric Oxide / metabolism
  • Nitric Oxide Synthase Type II / metabolism
  • Signal Transduction
  • Zebrafish / metabolism

Substances

  • NF-kappa B
  • Lipopolysaccharides
  • Anti-Inflammatory Agents
  • Cytokines
  • Interleukin-6
  • Nitric Oxide
  • Nitric Oxide Synthase Type II
  • Cyclooxygenase 2

Grants and funding

This work was supported by a research grant from the Chuongbong Academic Research Fund of Jeju National University in 2012. The APC of the manuscript was funded by General Sir John Kotelawala Defence University.