Marine Drugs (Nov 2021)

Diterpenoids from the Brown Alga <i>Rugulopteryx okamurae</i> and Their Anti-Inflammatory Activity

  • Belén Cuevas,
  • Ana I. Arroba,
  • Carolina de los Reyes,
  • Laura Gómez-Jaramillo,
  • M. Carmen González-Montelongo,
  • Eva Zubía

DOI
https://doi.org/10.3390/md19120677
Journal volume & issue
Vol. 19, no. 12
p. 677

Abstract

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Brown algae of the Family Dictyotaceae produce an array of structurally diverse terpenoids, whose biomedical potential in the anti-inflammatory area has been scarcely explored. Herein, the chemical study of the alga Rugulopteryx okamurae has led to the isolation of ten new diterpenoids: rugukadiol A (1), rugukamurals A–C (2–4), and ruguloptones A–F (6–10). The structures of the new compounds were established by spectroscopic means. Compound 1 exhibits an unprecedented diterpenoid skeleton featuring a bridged tricyclic undecane system. Compounds 2–10 belong to the secospatane class of diterpenoids and differ by the oxygenated functions that they contain. In anti-inflammatory assays, the new diterpenoid 1 and the secospatanes 5 and 10 significantly inhibited the production of the inflammatory mediator NO in LPS-stimulated microglial cells Bv.2 and macrophage cells RAW 264.7. Moreover, compounds 1 and 5 were found to strongly inhibit the expression of Nos2 and the pro-inflammatory cytokine Il1b in both immune cell lines.

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