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白细胞介素-10通过降低脂多糖诱导大鼠急性肺损伤高迁移率组蛋白1释放产生保护作用
引用本文:张锋,高鹏飞,李紫薇,武昊天,王凯,刘功俭.白细胞介素-10通过降低脂多糖诱导大鼠急性肺损伤高迁移率组蛋白1释放产生保护作用[J].国际麻醉学与复苏杂志,2014,35(9):791-795.
作者姓名:张锋  高鹏飞  李紫薇  武昊天  王凯  刘功俭
作者单位:江苏省麻醉与镇痛应用技术重点实验室,徐州医学院江苏省麻醉学重点实验室,221004
摘    要:目的 旨在研究白细胞介素(interleukin,IL)-10对高迁移率组蛋白l(high mobility group protein 1,HMGB1)释放的影响及其肺保护作用,进而探讨IL-10在治疗急性肺损伤中的可能机制. 方法 采用腹腔注射脂多糖(lipopolysaccharide,LPS)致大鼠脓毒症急性肺损伤模型,健康SPF级雄性SD大鼠72只,体重180 g~220 g,采用随机数字表法,随机分为对照组即磷酸盐缓冲液(phosphate buffered solution,PBS)组(P组,6只)、急性肺损伤组即LPS组(L组,30只)、PBS+IL-10组(PI组,6只)、LPS+IL-10组(LI组,30只).P组和PI组腹腔注射等体积PBS的同时分别经由气道滴注5 ml的PBS和IL-10,L组和LI组腹腔注射LPS的同时分别经由气道滴注等体积的PBS和IL-10.L组和LI组注射LPS后的4、8、16、24 h和48 h分别检测各组大鼠肺湿/干重比(wet/dry weight ratio,W/D)和支气管肺泡灌洗液(bronchoalveolar lavage fluid,BALF)中总蛋白浓度,酶联免疫吸附实验法检测BALF中炎性因子肿瘤坏死因子-α(tumor necrosis factor-α,TNF-α)和IL-6水平,苏木精-伊红(hematoxylin-eosin,HE)染色观察肺组织的病理变化,Western Blot分析肺组织中HMGB1表达水平. 结果 腹腔注射LPS后,L组大鼠肺组织W/D和BALF中总蛋白浓度分别为(5.68±0.12) mg/L和(254±105) mg/L,与P组比较,分别增加了12%和297%(P<0.05),BALF中TNF-α和IL-6水平明显增加(P<0.05),HE染色显示在注射LPS后4h肺组织的细胞浸润达到峰值随后减少,肺组织中HMGB1水平升高(P<0.05);使用IL-10后,LI组肺组织W/D和BALF中总蛋白浓度分别为(5.28±0.14) mg/L和(109±48) mg/L,与L组比较,分别降低了7%和57% (P<0.05),BALF中炎性因子水平降低(P<0.05),肺组织细胞浸润改善,HMGB1表达下调(P<0.05). 结论 IL-10对急性肺损伤具有保护作用,其机制可能为降低BALF中炎性因子的水平,下调晚期炎症介质HMGB1的表达,从而改善肺组织的细胞?

关 键 词:白细胞介素-10  脂多糖  急性肺损伤  高迁移率组蛋白1

The protective effect of interleukin-10 on lipopolysaccharide-induced acute lung injury in rats by attenuating the release of extracellular high mobility group protein 1
Zhang Feng , Gao Pengfei , Li Ziwei , Wu Haotian , Wang Kai , Liu Gongjian.The protective effect of interleukin-10 on lipopolysaccharide-induced acute lung injury in rats by attenuating the release of extracellular high mobility group protein 1[J].international journal of anesthesiology and resuscitation,2014,35(9):791-795.
Authors:Zhang Feng  Gao Pengfei  Li Ziwei  Wu Haotian  Wang Kai  Liu Gongjian
Institution:( Jiangsu Province Key Laboratory of Anesthesiology Xuzhou Medical College, Jiangsu Province Key Laboratory of Anesthesiology and Analgesia Application Technology, Xuzhou 221004, China)
Abstract:Objective This study aimed to investigate the effect of interleukin (IL)-10 on extracellular release of high mobility group protein 1 (HMGB1) in lipopolysaccharide (LPS)-induced acute lung injury in rats and its possible mechanism.Methods LPS (5 mg/kg,ip) induced acute lung injury model was used in our experiment,the healthy male Sprague-Dawley rats,weighed 180 g-220 g,were randomly divided into four groups:control group only used phosphate buffered solution (PBS) (group P,n=6),PBS+IL-10 group (group PI,n=6),acute lung injury group also LPS group (group L,n=30),LPS+interleukin-10 group(group LI,n=30).In the group L and LI,4,8,16,24 h and 48 h after the injection of LPS,the lung wet/dry weight ratio(W/D) and the concentration of the total protein in bronchoalveolar lavage fluid (BALF) were analyzed.The cytokines tumor necrosis factor-α(TNF-α) and IL-6] in bronchoalveolar lavage fluid were detected by enzyme-linked immunosorbent assay.Hitophathological changes in lung tissue were observed by hematoxylin-eosin staining,and the expression of HMGB1 was analyzed by Western Blot.Results After using of LPS,the W/D and the concentration of the total protein in BALF in group L were (5.68±0.12) mg/L and (254± 105)mg/L,which were increased by 12% and 297%(P〈0.05),compared with the group P,the concentration of TNF-α and IL-6 in BALF,HE staining of the lung tissue infiltration and the expression of HMGB1 in the lung tissue were all increased (P〈0.05).However after the intratracheal spray of IL-10,the W/D and the concentration of the total protein in BALF in group LI were (5.28±0.14) mg/L and (109±48) mg/L,which were decreased by 7% and 57%(P〈0.05),compared with the group L,the level of inflammatory factors,lung tissue infiltration and the concentration of HMGB1 were all decreased (P<0.05).Conclusions IL-10 can attenuate the injury induced by LPS in acute lung injury.The mechanism may be due to the effect of decreasing the p
Keywords:Interleukin-10  Lipopolysaccharide  Acute lung injury  High mobility group protein 1
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