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人支气管上皮细胞中α和β糖皮质激素受体mRNA的体外和体内调节

In vitro and in vivo modulation of alpha- and beta-glucocorticoid-receptor mRNA in human bronchial epithelium.

作者信息

Korn S H, Wouters E F, Wesseling G, Arends J W, Thunnissen F B

机构信息

Department of Pulmonology, University of Limburg, Maastricht, The Netherlands.

出版信息

Am J Respir Crit Care Med. 1997 Mar;155(3):1117-22. doi: 10.1164/ajrccm.155.3.9116996.

Abstract

Despite the central role bronchial epithelial cells play in asthmatic reactions, and the widespread use of inhaled corticosteroids in asthma, no information is available on the effect of glucocorticoids on glucocorticoid- receptor (GR) gene expression. In this study, the effect of budesonide on alpha- and beta-GR gene expression in human bronchial epithelial cells was investigated in vitro and in vivo. A bronchial epithelial cell line was exposed in vitro to budesonide, and a dose- and time-dependent synchronous downregulation of alpha- and beta-GR mRNA was observed. A 1-h exposure resulted in a reversible and reduced downregulation as compared with continuous exposure. In healthy volunteers (n = 10), no difference on average was present in GR mRNA expression before or after 4 wk of budesonide inhalation in either bronchial epithelial cells or alveolar macrophages. The time between the last inhalation and sampling of cells ranged from 0.5 to 8 h. However, a significant downregulation of alpha-GR mRNA was observed when the time between the last inhalation and sampling of cells was more than 2 h. Normalization of the downregulation of GR mRNA expression in bronchial epithelial cells is explained by the pharmacokinetics of inhaled budesonide in the human lung.

摘要

尽管支气管上皮细胞在哮喘反应中起核心作用,且吸入性糖皮质激素在哮喘治疗中广泛应用,但关于糖皮质激素对糖皮质激素受体(GR)基因表达的影响尚无相关信息。在本研究中,对布地奈德在体外和体内对人支气管上皮细胞中α-和β-GR基因表达的影响进行了研究。一种支气管上皮细胞系在体外暴露于布地奈德,观察到α-和β-GR mRNA呈剂量和时间依赖性同步下调。与持续暴露相比,1小时的暴露导致可逆且下调程度较小。在健康志愿者(n = 10)中,吸入布地奈德4周前后,支气管上皮细胞或肺泡巨噬细胞中的GR mRNA表达平均无差异。最后一次吸入与细胞采样之间的时间为0.5至8小时。然而,当最后一次吸入与细胞采样之间的时间超过2小时时,观察到α-GR mRNA有显著下调。支气管上皮细胞中GR mRNA表达下调的恢复正常可通过吸入性布地奈德在人肺中的药代动力学来解释。

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