Consequences of altered eicosanoid patterns for nociceptive processing in mPGES-1-deficient mice

J Cell Mol Med. 2008 Apr;12(2):639-48. doi: 10.1111/j.1582-4934.2007.00110.x.

Abstract

Cyclooxygenase-2 (COX-2)-dependent prostaglandin (PG) E(2) synthesis in the spinal cord plays a major role in the development of inflammatory hyperalgesia and allodynia. Microsomal PGE(2) synthase-1 (mPGES-1) isomerizes COX-2-derived PGH(2) to PGE(2). Here, we evaluated the effect of mPGES-1-deficiency on the nociceptive behavior in various models of nociception that depend on PGE(2) synthesis. Surprisingly, in the COX-2-dependent zymosan-evoked hyperalgesia model, the nociceptive behavior was not reduced in mPGES-1-deficient mice despite a marked decrease of the spinal PGE(2) synthesis. Similarly, the nociceptive behavior was unaltered in mPGES-1-deficient mice in the formalin test. Importantly, spinal cords and primary spinal cord cells derived from mPGES-1-deficient mice showed a redirection of the PGE(2) synthesis to PGD(2), PGF(2alpha) and 6-keto-PGF(1alpha) (stable metabolite of PGI(2)). Since the latter prostaglandins serve also as mediators of nociception they may compensate the loss of PGE(2) synthesis in mPGES-1-deficient mice.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Behavior, Animal*
  • Cells, Cultured
  • Culture Media / chemistry
  • Cyclooxygenase 1 / deficiency*
  • Cyclooxygenase 1 / genetics
  • Eicosanoids / metabolism*
  • Female
  • Hyperalgesia* / genetics
  • Immunohistochemistry
  • Macrophages, Peritoneal / cytology
  • Macrophages, Peritoneal / metabolism
  • Male
  • Membrane Proteins / deficiency*
  • Membrane Proteins / genetics
  • Mice
  • Mice, Knockout
  • Mice, Transgenic
  • Pain Measurement*
  • Spinal Cord / cytology
  • Spinal Cord / embryology
  • Spinal Cord / metabolism

Substances

  • Culture Media
  • Eicosanoids
  • Membrane Proteins
  • Cyclooxygenase 1
  • Ptgs1 protein, mouse