Respiratory Medicine Unit, Department of Medicine Solna and CMM, Karolinska Institutet and Karolinska University Hospital Solna Stockholm, Sweden.
AstraZeneca R&D Mölndal Mölndal, Sweden.
Pharmacol Res Perspect. 2014 Aug;2(4):e00054. doi: 10.1002/prp2.54. Epub 2014 Jun 12.
This study describes for the first time the expression levels of genes encoding membrane transporters and drug-metabolizing enzymes in the lungs of ex-smoking patients with chronic obstructive pulmonary disease (COPD). Membrane transporters and drug-metabolizing enzymes are key determinants of drug uptake, metabolism, and elimination for systemically administered as well as inhaled drugs, with consequent influence on clinical efficacy and patient safety. In this study, while no difference in gene expression was found between healthy and COPD subjects, we identified a significant regional difference in mRNA expression of both membrane transporters and drug-metabolizing enzymes between central and peripheral tissue in both healthy and COPD subjects. The majority of the differentially expressed genes were higher expressed in the central airways such as the transporters SLC2A1 (GLUT1), SLC28A3 (CNT3), and SLC22A4 (OCTN1) and the drug-metabolizing enzymes GSTZ1, GSTO2, and CYP2F1. Together, this increased knowledge of local pharmacokinetics in diseased and normal lung may improve modeling of clinical outcomes of new chemical entities intended for inhalation therapy delivered to COPD patients. In addition, based on the similarities between COPD and healthy subjects regarding gene expression of membrane transporters and drug-metabolizing enzymes, our results suggest that clinical pharmacological studies in healthy volunteers could be a valid model of COPD patients regarding drug disposition of inhaled drugs in terms of drug metabolism and drug transporters.
这项研究首次描述了慢性阻塞性肺疾病(COPD)戒烟患者肺部编码膜转运体和药物代谢酶的基因表达水平。膜转运体和药物代谢酶是系统给予和吸入药物摄取、代谢和消除的关键决定因素,因此对临床疗效和患者安全性有影响。在这项研究中,虽然健康受试者和 COPD 受试者之间的基因表达没有差异,但我们在健康和 COPD 受试者的中央和外周组织中均发现了膜转运体和药物代谢酶的 mRNA 表达存在显著的区域性差异。大多数差异表达的基因在中央气道中表达更高,如转运体 SLC2A1(GLUT1)、SLC28A3(CNT3)和 SLC22A4(OCTN1)以及药物代谢酶 GSTZ1、GSTO2 和 CYP2F1。总的来说,对疾病和正常肺部局部药代动力学的这一深入了解,可能会改善旨在用于 COPD 患者吸入治疗的新化学实体的临床结果模型。此外,基于 COPD 患者和健康受试者在膜转运体和药物代谢酶的基因表达方面的相似性,我们的结果表明,在药物代谢和药物转运体方面,针对吸入药物的药物处置,健康志愿者的临床药理学研究可能是 COPD 患者的有效模型。