FXR agonist GW4064 increases plasma glucocorticoid levels in C57BL/6 mice

Mol Cell Endocrinol. 2012 Oct 15;362(1-2):69-75. doi: 10.1016/j.mce.2012.05.010. Epub 2012 May 27.

Abstract

Since high expression of farnesoid X receptor (FXR) has been detected in glucocorticoid-producing adrenocortical cells, we evaluated the potential role of FXR in adrenal glucocorticoid production. FXR agonist GW4064 increased fasting plasma corticosterone levels (+45%; P<0.01) in C57BL/6 mice, indicative of enhanced adrenal steroidogenesis. GW4064 treatment did not affect plasma ACTH levels, adrenal weight, or adrenal expression of steroidogenic genes. Scavenger receptor BI (SR-BI) mRNA and protein expression, respectively, increased 1.9-fold (P<0.01) and 1.5-fold, which suggests a stimulated lipoprotein-associated cholesterol uptake into the adrenals upon GW4064 treatment. In line with an enhanced flux of cellular cholesterol into the steroidogenic pathway, adrenal unesterified and esterified cholesterol stores were 21-41% decreased (P<0.01) upon GW4064 treatment. In conclusion, we have shown that the FXR agonist GW4064 stimulates plasma corticosterone levels in C57BL/6 mice. Our findings suggest a novel role for FXR in the modulation of adrenal cholesterol metabolism and glucocorticoid synthesis in mice.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenal Glands / anatomy & histology
  • Adrenal Glands / drug effects
  • Adrenal Glands / metabolism
  • Adrenocorticotropic Hormone / blood*
  • Animals
  • Apolipoproteins A / genetics
  • Apolipoproteins A / metabolism
  • Cholesterol Side-Chain Cleavage Enzyme / genetics
  • Cholesterol Side-Chain Cleavage Enzyme / metabolism
  • Corticosterone / blood*
  • Female
  • Glucocorticoids / blood*
  • Isoxazoles / pharmacology*
  • Lipid Metabolism
  • Lipids / blood
  • Liver / metabolism
  • Membrane Transport Proteins / genetics
  • Membrane Transport Proteins / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Organ Size / drug effects
  • Phosphoenolpyruvate Carboxykinase (ATP) / genetics
  • Phosphoenolpyruvate Carboxykinase (ATP) / metabolism
  • Progesterone Reductase / genetics
  • Progesterone Reductase / metabolism
  • Receptor, Melanocortin, Type 2 / genetics
  • Receptor, Melanocortin, Type 2 / metabolism
  • Receptors, Cytoplasmic and Nuclear / agonists*
  • Receptors, Cytoplasmic and Nuclear / genetics
  • Receptors, Cytoplasmic and Nuclear / metabolism
  • Scavenger Receptors, Class B / genetics
  • Scavenger Receptors, Class B / metabolism
  • Steroid 11-beta-Hydroxylase / genetics
  • Steroid 11-beta-Hydroxylase / metabolism
  • Steroid 21-Hydroxylase / genetics
  • Steroid 21-Hydroxylase / metabolism
  • Tryptophan Oxygenase / genetics
  • Tryptophan Oxygenase / metabolism

Substances

  • Apolipoproteins A
  • Glucocorticoids
  • Isoxazoles
  • Lipids
  • Membrane Transport Proteins
  • Receptor, Melanocortin, Type 2
  • Receptors, Cytoplasmic and Nuclear
  • Scarb1 protein, mouse
  • Scavenger Receptors, Class B
  • apolipoprotein A-IV
  • organic solute transporter beta, mouse
  • farnesoid X-activated receptor
  • Adrenocorticotropic Hormone
  • 3 beta-hydroxysteroid dehydrogenase type II
  • Progesterone Reductase
  • Tryptophan Oxygenase
  • Cyp21a1 protein, mouse
  • Steroid 21-Hydroxylase
  • Steroid 11-beta-Hydroxylase
  • Cholesterol Side-Chain Cleavage Enzyme
  • Phosphoenolpyruvate Carboxykinase (ATP)
  • GW 4064
  • Corticosterone