In vivo modulation of glucocorticoid receptor mRNA by inhaled fluticasone propionate in bronchial mucosa and blood lymphocytes in subjects with mild asthma

J Allergy Clin Immunol. 1999 Apr;103(4):595-600. doi: 10.1016/s0091-6749(99)70230-7.

Abstract

Background: In vivo regulation of the glucocorticoid receptor (GR) by glucocorticoids provides a means of modulating sensitivity of targeted cells.

Objective: We sought to determine the in vivo modulation of GR mRNA expression by fluticasone propionate (FP) in subjects with mild asthma.

Methods: Ten atopic asthmatic subjects were treated with FP 250 microg twice daily for 4 weeks. Before and after treatment, the patients underwent fiberoptic bronchoscopy with endobronchial biopsy and sampling of venous blood for measurements of GR mRNA levels. A solution hybridization assay was used for quantitative analysis of GR mRNA. In addition, a 24-hour urinary cortisol excretion and an adrenocorticotropic hormone test before and after treatment with FP were performed.

Results: A high interindividual variation in GR mRNA expression was seen. However, we detected a significant reduction of the GR mRNA levels in the endobronchial biopsy specimens after FP treatment (36.6 +/- 23.1 and 25.0 +/- 10.9 amol GR mRNA/microg RNA, respectively; P <.01). In the peripheral blood lymphocytes an even more striking downregulation of the GR by its cognate ligand was documented (30.3 +/- 26.5 and 8.8 +/- 5 amol GR mRNA/microg RNA, respectively; P <.001), possibly reflecting differences in glucocorticoid sensitivity between tissues. A small but significant reduction of the 24-hour urinary cortisol excretion was observed (233 +/- 109 and 157 +/- 66 nmol/L, respectively; P <.01), whereas the feedback regulation of glucocorticoid synthesis by means of the hypothalamic-pituitary-adrenal axis as assessed by the adrenocorticotropic hormone test remained normal after treatment with FP.

Conclusion: The results in this study confirm the potency of the inhaled corticosteroid FP and provide evidence for a considerable tissue-specific interindividual variation in the expression of the GR.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenocorticotropic Hormone
  • Adult
  • Androstadienes / administration & dosage*
  • Androstadienes / pharmacology
  • Anti-Asthmatic Agents / administration & dosage*
  • Anti-Asthmatic Agents / pharmacology
  • Asthma / drug therapy*
  • Asthma / metabolism
  • Blotting, Western
  • Bronchi / metabolism*
  • Bronchoalveolar Lavage Fluid / cytology
  • Down-Regulation
  • Electrophoresis, Polyacrylamide Gel
  • Female
  • Fluticasone
  • Humans
  • Hydrocortisone / urine
  • Lymphocytes / metabolism*
  • Male
  • Mucous Membrane / metabolism
  • Peak Expiratory Flow Rate
  • Proteins / metabolism
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Receptors, Glucocorticoid / drug effects
  • Receptors, Glucocorticoid / genetics
  • Receptors, Glucocorticoid / metabolism*
  • Uteroglobin*

Substances

  • Androstadienes
  • Anti-Asthmatic Agents
  • Proteins
  • RNA, Messenger
  • Receptors, Glucocorticoid
  • SCGB1A1 protein, human
  • Adrenocorticotropic Hormone
  • Uteroglobin
  • Fluticasone
  • Hydrocortisone