Barnes Peter J
National Heart and Lung Institute, Imperial College School of Medicine, Dovehouse Street, London SW3 6LY, UK.
Curr Opin Pharmacol. 2008 Jun;8(3):300-7. doi: 10.1016/j.coph.2008.03.001. Epub 2008 May 3.
The mainstay of current drug therapy is long-acting bronchodilators; several longer acting inhaled beta(2)-agonists and muscarinic antagonists (and combinations) are now in development. No treatments reduce the progression or suppress the inflammation of COPD. With better understanding of the inflammatory and destructive process, several new targets have been identified. Several mediator antagonists tested in COPD have been disappointing, but of CXCR2 antagonists that block pulmonary neutrophil and monocyte recruitment may be more promising. Broad spectrum anti-inflammatory drugs may be more effective, and include inhibitors of PDE4, p38 MAPK and NF-kappaB, but side effects will be a major limitation so that inhaled delivery will be necessary. Perhaps the most promising approach is reversal corticosteroid resistance through increasing HDAC2 activity. This may be achieved by theophylline-like drugs, more effective antioxidants and non-antibiotic macrolides.
目前药物治疗的主要手段是长效支气管扩张剂;几种作用时间更长的吸入性β₂受体激动剂和毒蕈碱拮抗剂(以及联合制剂)目前正在研发中。尚无治疗方法能减缓慢性阻塞性肺疾病(COPD)的进展或抑制其炎症反应。随着对炎症和破坏过程的深入了解,已确定了几个新的靶点。在COPD中进行测试的几种介质拮抗剂效果不佳,但阻断肺部中性粒细胞和单核细胞募集的CXCR2拮抗剂可能更具前景。广谱抗炎药物可能更有效,包括磷酸二酯酶4(PDE4)、p38丝裂原活化蛋白激酶(MAPK)和核因子κB(NF-κB)的抑制剂,但副作用将是一个主要限制因素,因此有必要采用吸入给药方式。也许最有前景的方法是通过增加组蛋白去乙酰化酶2(HDAC2)的活性来逆转皮质类固醇抵抗。这可以通过类似茶碱的药物、更有效的抗氧化剂和非抗生素大环内酯类药物来实现。