Andersson O, Cassel T N, Grönneberg R, Brönnegård M, Stierna P, Nord M
Department of Lung Medicine, Karolinska Institute, Huddinge University Hospital, Huddinge, Sweden.
J Allergy Clin Immunol. 1999 Apr;103(4):595-600. doi: 10.1016/s0091-6749(99)70230-7.
In vivo regulation of the glucocorticoid receptor (GR) by glucocorticoids provides a means of modulating sensitivity of targeted cells.
We sought to determine the in vivo modulation of GR mRNA expression by fluticasone propionate (FP) in subjects with mild asthma.
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.
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.
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.
糖皮质激素在体内对糖皮质激素受体(GR)的调节为调控靶细胞的敏感性提供了一种方式。
我们试图确定丙酸氟替卡松(FP)对轻度哮喘患者体内GR mRNA表达的调节作用。
10名特应性哮喘患者每日两次吸入250μg FP,共治疗4周。治疗前后,患者接受纤维支气管镜检查及支气管内活检,并采集静脉血以测定GR mRNA水平。采用溶液杂交试验对GR mRNA进行定量分析。此外,在FP治疗前后进行24小时尿皮质醇排泄及促肾上腺皮质激素试验。
观察到GR mRNA表达存在较高的个体间差异。然而,我们检测到FP治疗后支气管内活检标本中GR mRNA水平显著降低(分别为36.6±23.1和25.0±10.9 amol GR mRNA/μg RNA;P<.01)。在外周血淋巴细胞中,其同源配体对GR的下调作用更为显著(分别为30.3±26.5和8.8±5 amol GR mRNA/μg RNA;P<.001),这可能反映了不同组织间糖皮质激素敏感性的差异。观察到24小时尿皮质醇排泄有小幅但显著的降低(分别为233±109和157±66 nmol/L;P<.01),而通过促肾上腺皮质激素试验评估的下丘脑 - 垂体 - 肾上腺轴对糖皮质激素合成的反馈调节在FP治疗后仍保持正常。
本研究结果证实了吸入性糖皮质激素FP的效力,并为GR表达存在显著的组织特异性个体间差异提供了证据。