4.7 Article

Anti-Inflammatory Effects of 5α,8α-Epidioxycholest-6-en-3β-ol, a Steroidal Endoperoxide Isolated from Aplysia depilans, Based on Bioguided Fractionation and NMR Analysis

Journal

MARINE DRUGS
Volume 17, Issue 6, Pages -

Publisher

MDPI
DOI: 10.3390/md17060330

Keywords

Aplysia depilans; 5 alpha; 8 alpha-epidioxycholest-6-en-3 beta-ol; iNOS; COX-1; COX-2; IL-6; TNF-alpha

Funding

  1. FCT/MCTES through national funds [UID/QUI/50006/2019]
  2. [PD/BD/113565/2015]
  3. Fundação para a Ciência e a Tecnologia [PD/BD/113565/2015] Funding Source: FCT

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Sea hares of Aplysia genus are recognized as a source of a diverse range of metabolites. 5 alpha ,8 alpha -Endoperoxides belong to a group of oxidized sterols commonly found in marine organisms and display several bioactivities, including antimicrobial, anti-tumor, and immunomodulatory properties. Herein we report the isolation of 5 alpha ,8 alpha -epidioxycholest-6-en-3 beta -ol (EnP(5,8)) from Aplysia depilans Gmelin, based on bioguided fractionation and nuclear magnetic resonance (NMR) analysis, as well as the first disclosure of its anti-inflammatory properties. EnP(5,8) revealed capacity to decrease cellular nitric oxide (NO) levels in RAW 264.7 macrophages treated with lipopolysaccharide (LPS) by downregulation of the Nos2 (inducible nitric oxide synthase, iNOS) gene. Moreover, EnP(5,8) also inhibited the LPS-induced expression of cyclooxygenase-2 (COX-2), interleukin 6 (IL-6), and tumor necrosis factor alpha (TNF-alpha) at the mRNA and protein levels. Mild selective inhibition of COX-2 enzyme activity was also evidenced. Our findings provide evidence of EnP(5,8) as a potential lead drug molecule for the development of new anti-inflammatory agents.

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