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瞬时受体电位香草素 4 的激活通过释放半胱氨酰白三烯收缩人支气管。

Transient receptor potential vanilloid 4 activation constricts the human bronchus via the release of cysteinyl leukotrienes.

机构信息

Respiratory Therapy Area, GlaxoSmithKline Pharmaceuticals, King of Prussia, Pennsylvania (M.A.M., M.A.L., G.E.H.); and Johns Hopkins Medical Institutions, Johns Hopkins University, Baltimore, Maryland (B.J.U.).

出版信息

J Pharmacol Exp Ther. 2014 Apr;349(1):118-25. doi: 10.1124/jpet.113.210203. Epub 2014 Feb 6.

Abstract

Prior studies have demonstrated that the ion channel transient receptor potential vanilloid 4 (TRPV4) is functionally expressed in airway smooth muscle cells and that TRPV4 single nucleotide polymorphisms are associated with airflow obstruction in patients with chronic obstructive pulmonary disease. We sought to use isometric tension measurements in ex vivo airways to determine whether short-term pharmacological activation of TRPV4 with the potent agonist GSK1016790 [N-((1S)-1-{[4-((2S)-2-{[(2,4-dichlorophenyl)sulfonyl]amino}-3-hydroxypropanoyl)-1-piperazinyl]carbonyl}-3-methylbutyl)-1-benzothiophene-2-carboxamide] would constrict human bronchial tissue. As predicted, transient receptor potential vanilloid 4 activation in the human airway produces contractions that are blocked by the nonselective transient receptor potential channel blocker ruthenium red. Moreover, the novel TRPV4-selective blocker GSK2334775 [(R)-6-(methylsulfonyl)-3-((4-(pyrrolidin-1-yl)piperindin-1-yl)methyl)-N-(2,2,2,-trifluoro-1-phenylethyl)-2-(3-(trifluoromethyl)phenyl)quinoline-4-carboxamide] inhibited these contractions over a concentration range consistent with its in vitro potency against recombinant and native TRPV4-containing channels. Surprisingly, TRPV4-dependent contractions were also blocked by a 5-lipoxygenase inhibitor and two structurally distinct cysteinyl leukotriene 1 receptor antagonists. In aggregate, our results fail to support the hypothesis that TRPV4 in airway smooth muscle cells regulates airway contractility short term. Rather, we provide pharmacological evidence that TRPV4 activation causes human airway constriction that is entirely dependent upon the production of cysteinyl leukotrienes. Together, these data identify a novel mechanism by which TRPV4 activation may contribute to pathologic remodeling and inflammation, in addition to airflow obstruction, in the diseased human respiratory tract.

摘要

先前的研究表明,离子通道瞬时受体电位香草素 4(TRPV4)在气道平滑肌细胞中功能性表达,并且 TRPV4 单核苷酸多态性与慢性阻塞性肺疾病患者的气流阻塞有关。我们试图使用离体气道的等长张力测量来确定用有效的激动剂 GSK1016790[ N-((1S)-1- {[4-((2S)-2- {[(2,4-二氯苯基)磺酰基]氨基}-3-羟基丙酰基)-1-哌嗪基]羰基}-3-甲基丁基)-1-苯并噻吩-2-甲酰胺]短期药理学激活 TRPV4 是否会收缩人支气管组织。正如所预测的那样,瞬时受体电位香草素 4 在人类气道中的激活会产生收缩,而这种收缩可以被非选择性瞬时受体电位通道阻滞剂钌红阻断。此外,新型 TRPV4 选择性阻滞剂 GSK2334775[(R)-6-(甲基磺酰基)-3-((4-(吡咯烷-1-基)哌啶-1-基)甲基)-N-(2,2,2,-三氟-1-苯乙基)-2-(3-(三氟甲基)苯基)喹啉-4-甲酰胺]在与体外对重组和天然 TRPV4 通道的效力一致的浓度范围内抑制了这些收缩。令人惊讶的是,5-脂氧合酶抑制剂和两种结构上不同的半胱氨酰白三烯 1 受体拮抗剂也阻断了 TRPV4 依赖性收缩。总而言之,我们的结果不支持气道平滑肌细胞中的 TRPV4 短期调节气道收缩性的假设。相反,我们提供了药理学证据,证明 TRPV4 的激活会导致人类气道收缩,而这种收缩完全依赖于半胱氨酰白三烯的产生。总的来说,这些数据确定了 TRPV4 激活可能导致患病呼吸道除气流阻塞外,还导致病理性重塑和炎症的新机制。

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