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作 者:戴惠军 潘灵辉[1] 林飞[1] 葛万运[1] 李玮[1] 贺盛[1]
机构地区:[1]广西医科大学附属肿瘤医院麻醉科,南宁市530021
出 处:《中华麻醉学杂志》2013年第11期1386-1388,共3页Chinese Journal of Anesthesiology
基 金:国家自然科学基金(81060008);2012年广西研究生教育创新计划(YCSZ2012044)
摘 要:目的探讨呼吸机相关性肺损伤大鼠肺组织巨噬细胞移动抑制因子(MIF)mRNA表达的变化。方法成年雄性sD大鼠30只,体重235~260g,采用随机数字表法,将其分为3组(n=10):对照组(c组)、小潮气量机械通气组(S组)和大潮气量机械通气组(L组)。C组气管插管后保持自主呼吸;S组和L组气管插管后行机械通气,s组潮气量7ml/kg,L组潮气量40ml/kg,吸呼比1:1,通气频率80次/min,FiO2 100%。自主呼吸或机械通气4h收集支气管肺泡灌洗液,测定总蛋白浓度和WBC计数,采用ELISA法测定MIF、IL-6、IL-1β的浓度;然后处死大鼠,取肺组织,光镜下观察病理学改变,测定湿重/干重比(W/D比),采用RT-PCR测定MIFmRNA表达。结果与C组和s组比较,L组BALF中WBC计数、总蛋白、MIF、IL-6、IL-1β的浓度和肺组织W/D比、MIFmRNA表达升高(P〈0.05),发生病理学损伤;C组和S组间上述各指标比较差异无统计学意义(P〉0.05)。结论MIFinRNA表达上调可能参与了大鼠呼吸机相关性肺损伤的发生。Objective To investigate the changes in the expression of macrophage migration inhibitory factor (MIF) mRNA in a rat model of ventilator-induced lung injury. Methods Thirty adult male Sprague-Dawley rats, weighing 235-260 g, were randomly divided into 3 groups ( n = 10 each) using a random number table: con- trol group (group C), small tidal volume (VT ) mechanical ventilation group (group S) and large tidal volume me- chanical ventilation group (group L) . The animals were anesthetized with intraperitoneal ketamine 100 mg/kg, mi- dazolam 0.2 mg/kg and atropine 1.0 mg/kg. The rats were tracheostomized and spontaneous breathing was main- tained in group C, while the rats were tracheostomized and mechanically ventilated for 4 h in groups S and L. The tidal volume was 7 ml/kg (group S) or 40 ml/kg (group L),I: E was 1 : 1, RR was 80 bpm and FiO2 was 100% . At 4 h of spontaneous breathing or mechanical ventilation, broncho-alveolar lung lavage fluid (BALF) was collect- ed for determination of the total protein concentration; white blood cell (WBC) counts and concentrations of MIF, IL-6 and IL-1β (by ELISA). Then the rats were sacrificed and the lungs removed for microscopic examination and for determination of wet to dry lung weight ratio (W/D ratio) and expression of MIF mRNA (by RT-PCR). Results Compared with C and S groups, WBC counts, concentrations of total protein, MIF, IL-6 and IL-1β in BALF, and W/D ratio and expression of MIF mRNA in lung tissues were significantly increased in group L (P 〈 0.05). There was no significant difference in the indexes mentioned above between group C and group S ( P 〉 0.05 ). The pathological changes occurred in group L. Conclusion The up-regulation of MIF mRNA expression in lung tissues may be involved in the development of ventilator-induced lung injury in rats.
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