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Natural products as inhibitors of prostaglandin E2 and pro-inflammatory 5-lipoxygenase-derived lipid mediator biosynthesis
Authors:Andreas Koeberle  Oliver Werz
Institution:Chair of Pharmaceutical/Medicinal Chemistry, Institute of Pharmacy, Friedrich-Schiller-University Jena, Philosophenweg 14, Jena 07743, Germany
Abstract:Non-steroidal anti-inflammatory drugs (NSAIDs) inhibit prostanoid formation and represent prevalent therapeutics for treatment of inflammatory disorders. However, NSAIDs are afflicted with severe side effects, which might be circumvented by more selective suppression of pro-inflammatory eicosanoid biosynthesis. This concept led to dual inhibitors of microsomal prostaglandin E2 synthase (mPGES)-1 and 5-lipoxygenase that are crucial enzymes in the biosynthesis of pro-inflammatory prostaglandin E2 and leukotrienes. The potential of their dual inhibition in light of superior efficacy and safety is discussed. Focus is placed on natural products, for which direct inhibition of mPGES-1 and leukotriene biosynthesis has been confirmed.
Keywords:AA  arachidonic acid  ABA  AKBA  BA  boswellic acid  COX  cyclooxygenase  EGCG  epigallocatechin-3-gallate  FLAP  5-lipoxygenase-activating protein  H(P)ETE  hydro(pero)xyeicosatetraenoic acid  KBA  11-keto-boswellic acid  LO  lipoxygenase  LT  leukotriene  MC-A  myrtucommulone A  mPGES  NF  nuclear factor  PG  prostaglandin  (c)PL  (cytosolic) phospholipase  PUFA  polyunsaturated fatty acid  SPM  specialized pro-resolving mediator  Tx  thromboxane  Eicosanoid  Prostaglandin  Leukotriene  5-Lipoxygenase  5-Lipoxygenase-activating protein  Arachidonic acid  Cyclooxygenase  Polypharmacology  Natural product
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