Anti-inflammatory and anti-virus potential of poxytrins, especially protectin DX

Biochimie. 2020 Dec:179:281-284. doi: 10.1016/j.biochi.2020.09.008. Epub 2020 Sep 18.

Abstract

Poxytrins (Pufa Oxygenated Trienes) are dihydroxy derivatives from polyunsaturated fatty acids (PUFA) with adjacent hydroxyl groups to a conjugated triene having the specific E,Z,E geometry. They are made by the double action of one lipoxygenase or the combined actions of two lipoxygenases, followed by reduction of the resulting hydroperoxides with glutathione peroxidase. Because of their E,Z,E conjugated triene, poxytrins may inhibit inflammation associated with cyclooxygenase (COX) activities, and reactive oxygen species (ROS) formation. In addition of inhibiting COX activities, at least one poxytrin, namely protectin DX (PDX) from docosahexaenoic acid (DHA), has also been reported as able to inhibit influenza virus replication by targeting its RNA metabolism.

Publication types

  • Review

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / chemistry
  • Anti-Inflammatory Agents / pharmacology*
  • Antiviral Agents / chemistry
  • Antiviral Agents / pharmacology*
  • Brain / drug effects
  • Brain / metabolism
  • Docosahexaenoic Acids / chemistry
  • Docosahexaenoic Acids / pharmacology*
  • Fatty Acids, Unsaturated / chemistry
  • Fatty Acids, Unsaturated / pharmacology*
  • Humans
  • Prostaglandin-Endoperoxide Synthases / drug effects
  • Reactive Oxygen Species / metabolism
  • Virus Replication / drug effects

Substances

  • 10,17-dihydroxydocosa-4,7,11,13,15,19-hexaenoic acid
  • Anti-Inflammatory Agents
  • Antiviral Agents
  • Fatty Acids, Unsaturated
  • Reactive Oxygen Species
  • Docosahexaenoic Acids
  • Prostaglandin-Endoperoxide Synthases