Effect of retinoic acid on human adrenal corticosteroid synthesis

Life Sci. 2016 Apr 15:151:277-280. doi: 10.1016/j.lfs.2016.03.023. Epub 2016 Mar 12.

Abstract

Aims: Retinoic acid has recently yielded promising results in the treatment of Cushing's disease, i.e., excess cortisol secretion due to a pituitary corticotropin (ACTH)-secreting adenoma. In addition to its effect on the tumoral corticotrope cell, clinical results suggest an additional adrenal site of action. Aim of this study was to evaluate whether retinoic acid modulates cortisol synthesis and secretion by human adrenals in vitro.

Main methods: Primary cultures from 10 human adrenals specimens were incubated with 10nM, 100nM and 1μM retinoic acid with and without 10nM ACTH for 24h. Cortisol levels were measured by radioimmunoassay and CYP11A1, STAR and MC2R gene expression analyzed by real-time PCR.

Key findings: Retinoic acid increased cortisol secretion (149.5±33.01%, 151.3±49.45% and 129.3±8.32% control secretion for 10nM, 100nM and 1μM respectively, p<0.05) and potentiated STAR expression (1.51±0.22, 1.56±0.15 and 1.59±0.14 fold change over baseline, for 10nM, 100nM and 1μM respectively, p<0.05). Concurrently, retinoic acid markedly blunted constitutional and ACTH-induced MC2R expression (0.66±0.11, 0.62±0.08 and 0.53±0.07 fold change over baseline, for 10nM, 100nM and 1μM respectively, p<0.05; 0.71±0.10, 0.51±0.07 and 0.51±0.08 fold change over ACTH alone, for 10nM, 100nM and 1μM respectively, p<0.05). No effect on CYP11A1 was observed.

Significance: Retinoic acid stimulates cortisol synthesis and secretion in human adrenals and at the same time markedly blunts ACTH receptor transcription. These results reveal a novel, adrenal effect of retinoic acid which may contribute to its efficacy in patients with Cushing's disease.

Keywords: Adrenal; Cortisol; Cushing's syndrome; MC2R; Retinoic acid; STAR.

MeSH terms

  • Adrenal Glands / drug effects*
  • Adrenal Glands / metabolism*
  • Adrenocorticotropic Hormone / antagonists & inhibitors
  • Adrenocorticotropic Hormone / pharmacology
  • Cholesterol Side-Chain Cleavage Enzyme / biosynthesis
  • Dose-Response Relationship, Drug
  • Gene Expression / drug effects
  • Humans
  • Hydrocortisone / biosynthesis*
  • Hydrocortisone / metabolism*
  • Phosphoproteins / biosynthesis
  • Primary Cell Culture
  • Receptor, Melanocortin, Type 1 / biosynthesis
  • Tretinoin / pharmacology*

Substances

  • Phosphoproteins
  • Receptor, Melanocortin, Type 1
  • steroidogenic acute regulatory protein
  • Tretinoin
  • Adrenocorticotropic Hormone
  • Cholesterol Side-Chain Cleavage Enzyme
  • Hydrocortisone