目的:探讨表皮生长因子受体(EGFR)抑制剂对外源锌离子致大鼠呼吸道急性炎症的影响。方法:将100μmol/L硫酸锌溶液经气管灌注大鼠肺部复制动物炎症模型,于灌注后4h、8h和24h处死大鼠,以PBS为对照,分别测定支气管肺泡灌洗液(BALF)中白细胞计数、总蛋白、白细胞介素8(IL-8)以及乳酸脱氢酶(LDH)的含量,以选择炎症最明显的时间点。进一步用二甲基亚砜(DMSO)和EGFR抑制剂PD153035预灌注大鼠,观察其对硫酸锌溶液所致呼吸道炎症的影响。结果:不同灌注液作用后大鼠白细胞计数(F=12.149,P=0.002)和IL-8(F=48.680,P〈0.001)等炎症反应指标不同,不同时间点白细胞计数(F=29.569,P〈0.001)和IL-8(F=59.778,P〈0.001)等炎症反应指标也不同,硫酸锌灌注后8h为炎症反应最强的时间。不同预灌注液作用后大鼠白细胞计数(F=37.872,P〈0.001)和IL-8(F=24.347,P〈0.001)等炎症反应指标不同,PD153035能抑制炎症反应的强度。结论:EGFR抑制剂能有效抑制外源锌离子所致大鼠呼吸道急性炎症。
Aim:To determine the effects of EGFR inhibitor on zinc-induced acute airway inflammation in rats.Methods:Use acute airway inflammation animal model to ascertain the time points with the severest airway inflammation.100 μmol/L zinc sulfate was tracheally instilled into rat lungs with PBS as control.The rats were sacrificed 4,8,and 24 h after the instillation and lung lavage was conducted thereafter.The number of white blood cells and the levels of proteins,LDH,and IL-8 in lung lavage fluids were determined,respectively.Moreover,rats were pre-instilled with the EGFR inhibitor PD153035 prior to zinc sulfate instillation and the alterations in the severity of airway inflammation observed.Results:Different perfusates cause white blood cell number (F was 12.149,P was 0.002) and IL-8 (F was 48.680,P0.001) and other indicators of rats inflammation different,white blood cell number (F was 29.569,P0.001 ) and IL-8 (F was 59.778,P0.001) and other indicators of inflammation at different time points were different,inflammation was the strongest after zinc sulfate perfusion 8 h.Different pre-perfusates cause white blood cell number (F was 37.872,P0.001) and IL-8 (F was 24.347,P0.001) and other indicators of rats inflammation different,PD153035 can suppress the inflammation.Conclusion:The EGFR inhibitor can suppress zinc sulfate-induced airway inflammation.