1. Academic Validation
  2. Polycerasoidol, a Natural Prenylated Benzopyran with a Dual PPARα/PPARγ Agonist Activity and Anti-inflammatory Effect

Polycerasoidol, a Natural Prenylated Benzopyran with a Dual PPARα/PPARγ Agonist Activity and Anti-inflammatory Effect

  • J Nat Prod. 2019 Jul 26;82(7):1802-1812. doi: 10.1021/acs.jnatprod.9b00003.
Almudena Bermejo 1 2 Aida Collado 1 Isabel Barrachina 1 Patrice Marqués 1 3 Noureddine El Aouad 1 Xavier Franck 4 Francisco Garibotto 5 Catherine Dacquet 6 Daniel H Caignard 6 Fernando D Suvire 5 Ricardo D Enriz 5 Laura Piqueras 1 3 Bruno Figadère 7 María-Jesús Sanz 1 3 Nuria Cabedo 1 3 Diego Cortes 1
Affiliations

Affiliations

  • 1 Department of Pharmacology , University of Valencia , 46113 Valencia Spain.
  • 2 Center of Citriculture and Vegetal Production , IVIA , Moncada, 46100 Valencia , Spain.
  • 3 Institute of Health Research-INCLIVA , University Clinic Hospital of Valencia , 46010 Valencia , Spain.
  • 4 UMR CNRS 6014/FR 3038, COBRA, Université de Rouen , Mont-Saint-Aignan 76821 , France.
  • 5 Facultad de Química, Bioquímica y Farmacia , Universidad Nacional de San Luis-IMIBIO-SL-CONICET , Chacabuco 915 , San Luis , Argentina.
  • 6 Départament des Sciences Expérimentales , Institut de Recherches Servier , Suresnes 92150 , France.
  • 7 UMR CNRS 8076, LERMIT , Université Paris-Sud, UFR de Pharmacie , Châtenay-Malabry 92290 , France.
Abstract

Dual peroxisome proliferator-activated receptor-α/γ (PPARα/γ) agonists regulate both lipid and glucose homeostasis under different metabolic conditions and can exert anti-inflammatory activity. We investigated the potential dual PPARα/γ agonism of prenylated benzopyrans polycerasoidol (1) and polycerasoidin (2) and their derivatives for novel drug development. Nine semisynthetic derivatives were prepared from the natural polycerasoidol (1) and polycerasoidin (2), which were evaluated for PPARα, -γ, -δ and retinoid X receptor-α activity in transactivation assays. Polycerasoidol (1) exhibited potent dual PPARα/γ agonism and low cytotoxicity. Structure-activity relationship studies revealed that a free phenol group at C-6 and a carboxylic acid at C-9' were key features for dual PPARα/γ agonism activity. Molecular modeling indicated the relevance of these groups for optimal ligand binding to the PPARα and PPARγ domains. In addition, polycerasoidol (1) exhibited a potent anti-inflammatory effect by inhibiting mononuclear leukocyte adhesion to the dysfunctional endothelium in a concentration-dependent manner via RXRα/PPARγ interactions. Therefore, polycerasoidol (1) can be considered a hit-to-lead molecule for the further development of novel dual PPARα/γ agonists capable of preventing cardiovascular events associated with metabolic disorders.

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