Lipopolysaccharide-induced murine embryonic resorption involves changes in endocannabinoid profiling and alters progesterone secretion and inflammatory response by a CB1-mediated fashion

Mol Cell Endocrinol. 2015 Aug 15:411:214-22. doi: 10.1016/j.mce.2015.04.032. Epub 2015 May 6.

Abstract

Genital tract infections are a common complication of human pregnancy that can result in miscarriage. We have previously shown that a lipopolysaccharide (LPS) induces embryonic resorption in a murine model of inflammatory miscarriage. This is accompanied by a dramatic decrease in systemic progesterone levels associated with a robust pro-inflammatory response that results in embryo resorption. Here, we tested the hypothesis that the endogenous cannabinoid system (eCS), through cannabinoid receptor 1 (CB1), plays a role in regulating progesterone levels and, therefore, the pro-inflammatory response. We show that LPS treatment in pregnant mice causes significant changes in the eCS ligands, which are reversed by progesterone treatment. We further show the CB1-KO mice maintain higher plasma progesterone levels after LPS treatment, which is associated with a feebler uterine inflammatory response and a significant drop in embryo resorption. These data suggest that manipulation of CB1 receptors and/or ligands is a potential therapeutic avenue to decrease infection-induced miscarriage.

Keywords: CB1 knockout; Decidua; Embryotoxicity; Endocannabinoid system.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Disease Models, Animal
  • Embryo Loss / chemically induced
  • Embryo Loss / metabolism*
  • Endocannabinoids / metabolism*
  • Female
  • Lipopolysaccharides*
  • Mice
  • Mice, Knockout
  • Pregnancy
  • Progesterone / metabolism*
  • Receptor, Cannabinoid, CB1 / genetics
  • Receptor, Cannabinoid, CB1 / metabolism*

Substances

  • Endocannabinoids
  • Lipopolysaccharides
  • Receptor, Cannabinoid, CB1
  • Progesterone