机构地区:[1]华中科技大学同济医学院协和医院麻醉科,武汉430022
出 处:《中国危重病急救医学》2007年第2期73-76,I0001,共5页Chinese Critical Care Medicine
基 金:国家自然科学基金资助项目(30471661);山东省自然基金资助项目(Y2006C120)
摘 要:目的 探讨机械通气对大鼠肺泡巨噬细胞(AM)表面Toll样受体4(TLR4)表达的影响。方法 清洁级成年雄性SD大鼠18只,随机分为自主呼吸组(R组,n=6)、小潮气量(VT)机械通气组(M组,n=6)和大VT机械通气组(N组,n=6)。腹腔注射质量分数为20%的乌拉坦8mg/kg麻醉大鼠,行气管插管。机械通气呼吸机参数设定:M组:VT为6ml/kg,N组VT为40ml/kg,吸:呼为1:1,呼气末正压(PEEP)为0,吸入氧浓度(FiO2)为0.21。调整呼吸频率和潮气末二氧化碳分压(PETCO2)维持在35~45mmHg(1mmHg=0.133kPa)。实验3h结束,放血处死大鼠。监测实验开始及实验1、2和3h时动脉血气分析;并测定大鼠肺组织病理形态学积分、湿/干重(W/D)比值及支气管肺泡灌洗液(BALF)中自细胞计数(WBC)和肺蛋白通透性系数。用逆转录-聚合酶链反应(RT—PCR)测定AM表面的TLR4mRNA表达,用免疫组化法测定AM表面的TLR4蛋白表达。结果 N组实验1h时存在过度通气,pH升高、动脉血二氧化碳分压(PaCO2)降低(P均〈0.05),其他指标都在正常范围内。与R组比较,N组肺组织病理形态学积分、W/D比值,BALF中WBC和肺蛋白透性系数以及TLR4蛋白表达和TLR4mRNA表达均显著升高(P均〈0.01);M组改变差异均无显著性(P均〉0.05)。结论 大VT机械通气导致大鼠肺损伤,并使AM表面TLR4表达明显上调。小VT机械通气可避免上述改变的发生。Objective To investigate the effects of mechanical ventilation on Toll like receptor 4 (TLR4) in rat's alveolar macrophages (AM). Methods Eighteen depuratory -class adult male SD rats weighting 230- 240 g were randomly divided into three groups (n = 6): autonomous breathing group (R group), small tidal volume (VT) mechanical ventilation group (M group, VT= 6 ml/kg) and large VT mechanical ventilation group (N group, VT=40 ml/kg). The animals were anesthetized with intraperitoneal 20% urethane 8 ml/kg, tracheostomized and mechanically ventilated (inhalation : exhalation (I : E)= 1 : 1, with positive end - expiratory pressure (PEEP) = 0, fraction of inspired oxygen (FiO2) = 0.21]. The respiratory rate was adjusted, and end- tidal carbon dioxide partial pressure (PETCO2) was maintained at 35- 45 mm Hg (1 mm Hg= 0. 133 kPa). Arterial blood samples were taken for blood gas analysis at the beginning of the experiment and 1, 2 and 3 hours after the experiment. The experiment was terminated, and pathomorphology score, pulmonary tissue wet/dry (W/D) weight ratio, white blood cells count (WBC) in bronchoalveolar lavage fluid (BALF) were determined at 3 hours. The rats were sacrificed by bloodletting after experiment. Then the rats' BALF and pulmonary albumin permeability (PAP) were determined. The expression of AM TLR4 mRNA was assessed by semi -quantitative reverse transcription -polymerase chain reaction (RT- PCR). AM TLR4 protein expression was determined by immunohistochemistry. Results Over ventilation, elevated pH and lower partial pressure of carbon dioxide in arterial blood (PaCO2) were observed in N group at 1 hour, and other indexes were normal. The pulmonary pathomorphology score, pulmonary W/D weight ratio, WBC in BALF, PAP, and the mRNA expression of TLR4 and the protein of TLR4 in AM in the N group were greatly increased as compared with the R group (all P〈0. 01), while they were not significantly changed in the M grou
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