4.6 Article

Semisynthetic Abietic and Dehydroabietic Acid Derivatives and Triptoquinone Epimers Interfere with LPS-Triggered Activation of Dendritic Cells

Journal

MOLECULES
Volume 27, Issue 19, Pages -

Publisher

MDPI
DOI: 10.3390/molecules27196684

Keywords

abietane diterpenes; dehydroabietic acid; triptoquinone; cytokines; dendritic cells; surface co-stimulatory molecules

Funding

  1. Spanish Government (Consejo Superior de Investigaciones Cientificas) [201680I008]
  2. Colciencias [RC 366-2011, 1115-343-19225, 1115-459-21533, 1115-519-28906]
  3. Universidad de Antioquia [CODI 2014-1041, CPT-0411, EO-1204, CPT-0607]

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This study screened 23 known semi-synthetic derivatives of AA, DHA, and TQs for their inhibitory effects on pro-inflammatory cytokine production. Two DHA derivatives and two TQs showed significant anti-inflammatory properties and could inhibit the production of multiple pro-inflammatory cytokines.
Abietic acid (AA), dehydroabietic acid (DHA) and triptoquinones (TQs) are bioactive abietane-type diterpenoids, which are present in many edible vegetables and medicinal herbs with health-promoting properties. Evidence suggests that beneficial effects of diterpenes operate, at least in part, through effects on cells in the immune system. Dendritic cells (DCs) are a key type of leukocyte involved in the initiation and regulation of the immune/inflammatory response and natural or synthetic compounds that modulate DC functions could be potential anti-inflammatory/immunomodulatory agents. Herein, we report the screening of 23 known semisynthetic AA and DHA derivatives, and TQs, synthesized previously by us, in a multi-analyte DC-based assay that detects inhibition of pro-inflammatory cytokine production. Based on the magnitude of the inhibitory effect observed and the number of cytokines inhibited, a variety of activities among compounds were observed, ranging from inactive/weak to very potent inhibitors. Structurally, either alcohol or methyl ester substituents on ring A along with the introduction of aromaticity and oxidation in ring C in the abietane skeleton were found in compounds with higher inhibitory properties. Two DHA derivatives and two TQs exhibited a significant inhibition in all pro-inflammatory cytokines tested and were further investigated. The results confirmed their ability to inhibit, dose dependently, LPS-stimulated expression of the co-stimulatory molecules CD40 and/or CD86 and the production of the pro-inflammatory cytokines IL-1 beta, IL-6, IL-12 and TNF alpha. Our results demonstrate that DC maturation process can be targeted by semisynthetic DHA derivatives and TQ epimers and indicate the potential of these compounds as optimizable anti-inflammatory/immunomodulatory agents.

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