Meakins Christie Laboratories, Department of Medicine, McGill University, Montreal, QC H2X 2P2, Canada.
Free Radic Biol Med. 2011 Mar 1;50(5):602-8. doi: 10.1016/j.freeradbiomed.2010.12.001. Epub 2010 Dec 13.
New therapeutics designed as rescue treatments after toxic gas injury such as from chlorine (Cl(2)) are an emerging area of interest. We tested the effects of the metalloporphyrin catalytic antioxidant AEOL10150, a compound that scavenges peroxynitrite, inhibits lipid peroxidation, and has SOD and catalase-like activities, on Cl(2)-induced airway injury. Balb/C mice received 100ppm Cl(2) gas for 5 min. Four groups were studied: Cl(2) only, Cl(2) followed by AEOL10150 1 and 9 h after exposure, AEOL10150 only, and control. Twenty-four hours after Cl(2) gas exposure airway responsiveness to aerosolized methacholine (6.25-50mg/ml) was measured using a small-animal ventilator. Bronchoalveolar lavage (BAL) was performed to assess airway inflammation and protein. Whole lung tissue was assayed for 4-hydroxynonenal. In separate groups, lungs were collected at 72 h after Cl(2) injury to evaluate epithelial cell proliferation. Mice exposed to Cl(2) showed a significantly higher airway resistance compared to control, Cl(2)/AEOL10150, or AEOL10150-only treated animals in response to methacholine challenge. Eosinophils, neutrophils, and macrophages were elevated in BAL of Cl(2)-exposed mice. AEOL10150 attenuated the increases in neutrophils and macrophages. AEOL10150 prevented Cl(2)-induced increase in BAL fluid protein. Chlorine induced an increase in the number of proliferating airway epithelial cells, an effect AEOL10150 attenuated. 4-Hydroxynonenal levels in the lung were increased after Cl(2) and this effect was prevented with AEOL10150. AEOL10150 is an effective rescue treatment for Cl(2)-induced airway hyperresponsiveness, airway inflammation, injury-induced airway epithelial cell regeneration, and oxidative stress.
设计用于氯气(Cl(2))等有毒气体损伤后的救援治疗的新型治疗方法是一个新兴的研究领域。我们测试了金属卟啉催化抗氧化剂 AEOL10150 的效果,该化合物能清除过氧亚硝酸盐、抑制脂质过氧化,并具有 SOD 和过氧化氢酶样活性,对 Cl(2) 诱导的气道损伤。Balb/C 小鼠接受 100ppm Cl(2) 气体 5 分钟。研究了四组:仅 Cl(2)、暴露后 1 小时和 9 小时后 Cl(2) 加 AEOL10150、仅 AEOL10150 和对照。暴露于 Cl(2)气体 24 小时后,使用小动物呼吸机测量气道对雾化乙酰甲胆碱(6.25-50mg/ml)的反应性。进行支气管肺泡灌洗(BAL)以评估气道炎症和蛋白。测定全肺组织的 4-羟基壬烯醛。在单独的组中,在 Cl(2)损伤后 72 小时收集肺组织以评估上皮细胞增殖。与对照、Cl(2)/AEOL10150 或仅 AEOL10150 处理的动物相比,暴露于 Cl(2)的小鼠在对乙酰甲胆碱挑战时显示出明显更高的气道阻力。Cl(2)暴露小鼠的 BAL 中嗜酸性粒细胞、中性粒细胞和巨噬细胞升高。AEOL10150 减轻了中性粒细胞和巨噬细胞的增加。AEOL10150 防止了 Cl(2)诱导的 BAL 液蛋白增加。氯诱导增殖性气道上皮细胞数量增加,AEOL10150 减轻了这种作用。氯(Cl(2))后肺中 4-羟基壬烯醛水平增加,AEOL10150 可预防这种作用。AEOL10150 是 Cl(2) 诱导的气道高反应性、气道炎症、损伤诱导的气道上皮细胞再生和氧化应激的有效救援治疗方法。