Jia Yanlin, Lee Lu-Yuan
Neurobiology, Schering-Plough Research Institute, Kenilworth, NJ 07033, USA.
Biochim Biophys Acta. 2007 Aug;1772(8):915-27. doi: 10.1016/j.bbadis.2007.01.013. Epub 2007 Feb 1.
Transient receptor potential vanilloid type channels (TRPVs) are expressed in several cell types in human and animal lungs. Increasing evidence has demonstrated important roles of these cation channels, particularly TRPV1 and TRPV4, in the regulation of airway function. These TRPVs can be activated by a number of endogenous substances (hydrogen ion, certain lipoxygenase products, etc.) and changes in physiological conditions (e.g., temperature, osmolarity, etc.). Activation of these channels can evoke Ca(2+) influx and excitation of the neuron. TRPV1 channels are generally expressed in non-myelinated afferents innervating the airways and lungs, which also contain sensory neuropeptides such as tachykinins. Upon stimulation, these sensory nerves elicit centrally-mediated reflex responses as well as local release of tachykinins, and result in cough, airway irritation, reflex bronchoconstriction and neurogenic inflammation in the airways. Recent studies clearly demonstrated that the excitability of TRPV1 channels is up-regulated by certain autacoids (e.g., prostaglandin E(2), bradykinin) released during airway inflammatory reaction. Under these conditions, the TRPV1 can be activated by a slight increase in airway temperature or tissue acidity. Indirect evidence also suggests that TRPV channels may play a part in the pathogenesis of certain respiratory diseases such as asthma and chronic cough. Therefore, the potential use of TRPV antagonists as a novel therapy for these diseases certainly merits further investigation.
瞬时受体电位香草酸亚型通道(TRPVs)在人和动物肺部的多种细胞类型中均有表达。越来越多的证据表明,这些阳离子通道,尤其是TRPV1和TRPV4,在气道功能调节中发挥着重要作用。这些TRPVs可被多种内源性物质(氢离子、某些脂氧合酶产物等)以及生理条件的变化(如温度、渗透压等)激活。这些通道的激活可引起Ca(2+)内流并使神经元兴奋。TRPV1通道通常表达于支配气道和肺部的无髓传入神经中,这些神经还含有速激肽等感觉神经肽。受到刺激后,这些感觉神经会引发中枢介导的反射反应以及速激肽的局部释放,进而导致咳嗽、气道刺激、反射性支气管收缩和气道神经源性炎症。最近的研究清楚地表明,气道炎症反应过程中释放的某些自分泌物质(如前列腺素E(2)、缓激肽)会上调TRPV1通道的兴奋性。在这些情况下,气道温度或组织酸度的轻微升高即可激活TRPV1。间接证据还表明,TRPV通道可能在某些呼吸系统疾病如哮喘和慢性咳嗽的发病机制中起作用。因此,将TRPV拮抗剂作为这些疾病的新型治疗方法的潜在用途无疑值得进一步研究。