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

被引:14
作者
Andersson, O [1 ]
Cassel, TN
Grönneberg, R
Brönnegård, M
Stierna, P
Nord, M
机构
[1] Huddinge Univ Hosp, Karolinska Inst, Dept Lung Med, S-14186 Huddinge, Sweden
[2] Huddinge Univ Hosp, Karolinska Inst, Dept Med Nutr, S-14186 Huddinge, Sweden
[3] Huddinge Univ Hosp, Karolinska Inst, Dept Otorhinolaryngol, S-14186 Huddinge, Sweden
[4] Huddinge Univ Hosp, Karolinska Inst, Dept Pediat, S-14186 Huddinge, Sweden
关键词
glucocorticoid receptor; asthma; bronchoalveolar lavage; fluticasone; Clara cell secretory protein;
D O I
10.1016/S0091-6749(99)70230-7
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
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 mu g 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/mu g 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/mu g 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.
引用
收藏
页码:595 / 600
页数:6
相关论文
共 44 条
[1]   Glucocorticoid receptor localization in normal and asthmatic lung [J].
Adcock, IM ;
Gilbey, T ;
Gelder, CM ;
Chung, KF ;
Barnes, PJ .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1996, 154 (03) :771-782
[2]   PURIFICATION AND LEVEL OF EXPRESSION IN BRONCHOALVEOLAR LAVAGE OF A HUMAN POLYCHLORINATED BIPHENYL (PCB)-BINDING PROTEIN - EVIDENCE FOR A STRUCTURAL AND FUNCTIONAL KINSHIP TO THE MULTIHORMONALLY REGULATED PROTEIN UTEROGLOBIN [J].
ANDERSSON, O ;
NORDLUNDMOLLER, L ;
BRONNEGARD, M ;
SIRZEA, F ;
RIPE, E ;
LUND, J .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1991, 5 (01) :6-12
[3]  
ANDERSSON O, 1994, J BIOL CHEM, V269, P19081
[4]   GLUCOCORTICOID RECEPTOR-BETA, A POTENTIAL ENDOGENOUS INHIBITOR OF GLUCOCORTICOID ACTION IN HUMANS [J].
BAMBERGER, CM ;
BAMBERGER, AM ;
DECASTRO, M ;
CHROUSOS, GP .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (06) :2435-2441
[5]   GENE-REGULATION BY STEROID-HORMONES [J].
BEATO, M .
CELL, 1989, 56 (03) :335-344
[6]  
BOURGEOIS S, 1978, CANCER RES, V38, P4279
[7]  
BROERS JLV, 1992, LAB INVEST, V66, P337
[8]  
BRONNEGARD M, 1996, AM J RESP CRIT CARE, V154, pS32
[9]   NEGATIVE CROSS-TALK BETWEEN RELA AND THE GLUCOCORTICOID RECEPTOR - A POSSIBLE MECHANISM FOR THE ANTIINFLAMMATORY ACTION OF GLUCOCORTICOIDS [J].
CALDENHOVEN, E ;
LIDEN, J ;
WISSINK, S ;
VANDESTOLPE, A ;
RAAIJMAKERS, J ;
KOENDERMAN, L ;
OKRET, S ;
GUSTAFSSON, JA ;
VANDERSAAG, PT .
MOLECULAR ENDOCRINOLOGY, 1995, 9 (04) :401-412
[10]  
CATO ACB, 1985, ANTICANCER RES, V5, P65