Schaafsma Dedmer, Gosens Reinoud, Zaagsma Johan, Halayko Andrew J, Meurs Herman
Department of Physiology & Internal Medicine, and Section of Respiratory Disease, University of Manitoba, Winnipeg, Manitoba, Canada.
Eur J Pharmacol. 2008 May 13;585(2-3):398-406. doi: 10.1016/j.ejphar.2008.01.056. Epub 2008 Mar 18.
In asthma, inflammatory mediators that are released in the airways by recruited inflammatory cells and by resident structural cells result in airway hyperresponsiveness caused by increased bronchoconstriction. In addition, chronic inflammation appears to drive remodelling of the airways that contributes to the development of fixed airway obstruction and airway hyperresponsiveness in chronic asthma. Airway remodelling includes several key features such as excessive deposition of extracellular matrix proteins in the airway wall (fibrosis) and increased abundance of contractile airway smooth muscle encircling the airways. Current asthma therapy fails to inhibit these features satisfactorily. This review focuses on Rho kinase as a potential drug target in asthma, as compelling evidence from animal models and ex vivo studies suggests a central role for this enzyme and its associated signalling in acute and chronic airway hyperresponsiveness.
在哮喘中,募集的炎症细胞和固有结构细胞在气道中释放的炎症介质会导致支气管收缩增强,从而引起气道高反应性。此外,慢性炎症似乎会驱动气道重塑,这有助于慢性哮喘中固定性气道阻塞和气道高反应性的发展。气道重塑包括几个关键特征,如气道壁中细胞外基质蛋白过度沉积(纤维化)以及环绕气道的收缩性气道平滑肌数量增加。目前的哮喘治疗方法未能令人满意地抑制这些特征。本综述重点关注Rho激酶作为哮喘潜在的药物靶点,因为来自动物模型和体外研究的有力证据表明,这种酶及其相关信号在急性和慢性气道高反应性中起着核心作用。