Eynott Paul R, Nath Puneeta, Leung Sum-Yee, Adcock Ian M, Bennett Brydon L, Chung K Fan
National Heart & Lung Institute, Imperial College School of Medicine, Dovehouse St, London SW3 6LY.
Br J Pharmacol. 2003 Dec;140(8):1373-80. doi: 10.1038/sj.bjp.0705569. Epub 2003 Nov 17.
Chronic cellular inflammation and airway wall remodelling with subepithelial fibrosis and airway smooth muscle (ASM) cell hyperplasia are features of chronic asthma. Jun N-terminal kinase (JNK) may be implicated in these processes by regulating the transcriptional activity of activator protein (AP)-1. We examined the effects of an inhibitor of JNK, SP600125 (anthra [1,9-cd] pyrazole-6 (2 H)-one), in a model of chronic allergic inflammation in the rat. Rats sensitised to ovalbumin (OA) were exposed to OA-aerosol every third day on six occasions and were treated with SP600125 (30 mg kg-1 b.i.d; 360 mg in total) for 12 days, starting after the second through to the sixth OA exposure. We measured eosinophilic and T-cell inflammation in the airways, proliferation of ASM cells and epithelial cells by incorporation of bromodeoxyuridine (BrdU), and bronchial responsiveness to acetylcholine. SP600125 significantly reduced the number of eosinophils (P<0.05) and lymphocytes (P<0.05) in bronchoalveolar lavage fluid, suppressed eosinophilic (P<0.05) and CD2+ T-cell (P<0.05) infiltration within the bronchial submucosa, and the increased DNA incorporation in ASM (P<0.05) and epithelial cell incorporation (P<0.05). SP600125 did not alter bronchial hyper-responsiveness observed after chronic allergen exposure. Pathways regulated by JNK positively regulate ASM cell proliferation and allergic cellular inflammation following chronic allergen exposure.
慢性细胞炎症以及伴有上皮下纤维化和气道平滑肌(ASM)细胞增生的气道壁重塑是慢性哮喘的特征。c-Jun氨基末端激酶(JNK)可能通过调节活化蛋白(AP)-1的转录活性参与这些过程。我们在大鼠慢性过敏性炎症模型中研究了JNK抑制剂SP600125(蒽[1,9-cd]吡唑-6(2H)-酮)的作用。对卵清蛋白(OA)致敏的大鼠每隔一天暴露于OA气雾剂,共6次,并在第二次至第六次OA暴露后开始用SP600125(30mg/kg,每日两次;总共360mg)治疗12天。我们测量了气道中的嗜酸性粒细胞和T细胞炎症、通过掺入溴脱氧尿苷(BrdU)检测ASM细胞和上皮细胞的增殖以及支气管对乙酰胆碱的反应性。SP600125显著减少了支气管肺泡灌洗液中嗜酸性粒细胞数量(P<0.05)和淋巴细胞数量(P<0.05),抑制了支气管黏膜下层嗜酸性粒细胞浸润(P<0.05)和CD2+T细胞浸润(P<0.05),以及ASM细胞中DNA掺入增加(P<0.05)和上皮细胞掺入增加(P<0.05)。SP600125并未改变慢性过敏原暴露后观察到的支气管高反应性。JNK调节的信号通路在慢性过敏原暴露后正向调节ASM细胞增殖和过敏性细胞炎症。