Anti-Inflammatory Activity of Tanzawaic Acid Derivatives from a Marine-Derived Fungus Penicillium steckii 108YD142

Mar Drugs. 2016 Jan 8;14(1):14. doi: 10.3390/md14010014.

Abstract

Chemical investigation of a marine-derived fungus, Penicillium steckii 108YD142, resulted in the discovery of a new tanzawaic acid derivative, tanzawaic acid Q (1), together with four known analogues, tanzawaic acids A (2), C (3), D (4), and K (5). The structures of tanzawaic acid derivatives 1-5 were determined by the detailed analysis of 1D, 2D NMR and LC-MS data, along with chemical methods and literature data analysis. These compounds significantly inhibited nitric oxide (NO) production and the new tanzawaic acid Q (1) inhibited the lipopolysaccharide (LPS)-induced inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) proteins and mRNA expressions in RAW 264.7 macrophages. Additionally, compound 1 reduced the mRNA levels of inflammatory cytokines. Taken together, the results of this study demonstrated that the new tanzawaic acid derivative inhibits LPS-induced inflammation. This is the first report on the anti-inflammatory activity of tanzawaic acid Q (1).

Keywords: Penicillium steckii; anti-inflammatory; marine fungus; tanzawaic acids.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / chemistry
  • Anti-Inflammatory Agents / pharmacology*
  • Cyclooxygenase 2 / drug effects
  • Fatty Acids, Unsaturated / chemistry
  • Fatty Acids, Unsaturated / pharmacology*
  • Humans
  • Macrophages / drug effects
  • Mice
  • Naphthols / chemistry
  • Naphthols / pharmacology*
  • Nitric Oxide Synthase Type II / drug effects
  • Penicillium*
  • Seawater
  • Structure-Activity Relationship

Substances

  • Anti-Inflammatory Agents
  • Fatty Acids, Unsaturated
  • Naphthols
  • tanzawaic acid Q
  • Nitric Oxide Synthase Type II
  • Cyclooxygenase 2