Prostaglandin F2α FP receptor inhibitor reduces demyelination and motor dysfunction in a cuprizone-induced multiple sclerosis mouse model

Prostaglandins Leukot Essent Fatty Acids. 2014 Nov;91(5):175-82. doi: 10.1016/j.plefa.2014.08.004. Epub 2014 Sep 6.

Abstract

Previously, we have demonstrated that prostamide/PGF synthase, which catalyzes the reduction of prostaglandin (PG) H2 to PGF2α, is constitutively expressed in myelin sheaths and cultured oligodendrocytes, suggesting that PGF2α has functional significance in myelin-forming oligodendrocytes. To investigate the effects of PGF2α/FP receptor signaling on demyelination, we administrated FP receptor agonist and antagonist to cuprizone-exposed mice, a model of multiple sclerosis. Mice were fed a diet containing 0.2% cuprizone for 5 weeks, which induces severe demyelination, glial activation, proinflammatory cytokine expression, and motor dysfunction. Administration of the FP receptor antagonist AL-8810 attenuated cuprizone-induced demyelination, glial activation, and TNFα expression in the corpus callosum, and also improved the motor function. These data suggest that during cuprizone-induced demyelination, PGF2α/FP receptor signaling contributes to glial activation, neuroinflammation, and demyelination, resulting in motor dysfunction. Thus, FP receptor inhibition may be a useful symptomatic treatment in multiple sclerosis.

Keywords: Cuprizone (CPZ); Demyelination; Multiple sclerosis (MS); Neuroinflammation; Prostaglandin F(2α) receptor (FP).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Corpus Callosum / drug effects
  • Corpus Callosum / metabolism
  • Corpus Callosum / pathology
  • Cuprizone / toxicity
  • Demyelinating Diseases / metabolism*
  • Demyelinating Diseases / pathology
  • Dinoprost / administration & dosage
  • Dinoprost / analogs & derivatives
  • Disease Models, Animal
  • Humans
  • Mice
  • Motor Activity / drug effects
  • Motor Activity / genetics
  • Multiple Sclerosis / chemically induced
  • Multiple Sclerosis / drug therapy*
  • Multiple Sclerosis / metabolism*
  • Multiple Sclerosis / pathology
  • Myelin Sheath / metabolism
  • Oligodendroglia / metabolism
  • Prostaglandin H2 / metabolism
  • Receptors, Prostaglandin / metabolism*
  • Tumor Necrosis Factor-alpha / biosynthesis

Substances

  • Receptors, Prostaglandin
  • Tumor Necrosis Factor-alpha
  • prostaglandin F2alpha receptor
  • AL 8810
  • Prostaglandin H2
  • Cuprizone
  • Dinoprost