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微小RNA-146a对机械通气所致肺损伤大鼠肺组织TLR4炎症信号通路的影响及机制

[Effect and mechanism of MicroRNA-146a on TLR4 inflammatory signal pathway in the lung tissues of rats with mechanical ventilator-induced lung injury].

作者信息

Lin X, Xu L Y, Li X H, Yu T X, Lin Q, Chen L, Bao Y W

机构信息

Department of Respiratory Medicine, Affiliated Fuzhou First Hospital of Fujian Medical University, Fuzhou 350009, China.

出版信息

Zhonghua Yi Xue Za Zhi. 2018 Sep 11;98(34):2749-2753. doi: 10.3760/cma.j.issn.0376-2491.2018.34.014.

Abstract

To investigate the effect and mechanism of microRNA-146a (miR-146a) on Toll-Like Receptor 4 (TLR4) inflammatory signal pathway in the lung tissues of rats with mechanical ventilator-induced lung injury. Thirty-two healthy male Sprague-Dawley rats were randomly divided into 4 groups (=8 each): group A, normal control group, no mechanical ventilation, spontaneous breathing; group B, mechanical ventilation injury; group C, mechanical ventilation injury plus no-load virus transfection; group D, mechanical ventilation injury plus virus transfection; in group B, C, and D, mechanical ventilation were performed, respiratory rate was controlled at 80 beats/min, tidal volume was 40 ml/kg, inhaled oxygen concentration (FiO) was 21%, inhalation/expiration ratio was 1∶2, positive end expiratory pressure ventilation (PEEP) was 0, each group were ventilated 4 hours daily, 7 days continuously to establish ventilator induced lung injury (VILI) rat model. Paraffin-embedded sections of lung tissue were stained with HE, the morphology and damage of lung tissue were observed under microscope. The lungs wet and dry ratio (W/D), the levels of inflammatory cytokines interleukin (IL)-1β, IL-2 and tumor necrosis factor (TNF)-α were determined. Real-time PCR was used to detect the expression of TLR4 mRNA. The level of TLR4 protein was determined by Western blot. The levels of lung tissue W/D and lung injury scores in group B (6.41±0.10, 11.38±0.92), group C (6.45±0.19, 11.75±1.04), group D (5.95±0.14, 7.53±4.78) were significantly increased than those in group A (4.33±0.08, 0.25±0.46), and in group D they were significantly decreased than group C (all <0.01). The levels of IL-1β, IL-2, TNF-α in group B[(36.07±4.28) pg/ml, (5.02±0.63) ng/ml, (382.57±35.41) ng/ml], group C[(35.82±5.47) pg/ml, (4.98±0.71) ng/ml, (375.13±36.95) ng/ml], group D[(27.01±3.18) pg/ml, (3.96±0.82) ng/ml, (297.56±39.08) ng/ml]were significantly increased than those in group A[(21.46±3.15) pg/ml, (2.45±0.17) ng/ml, (195.92±18.07) ng/ml], and in group D they were significantly decreased than group C (all <0.01). The relative expression levels of TLR4 mRNA and TLR4 proteins in group B (29.57±5.10, 0.75±0.110), group C (27.27±4.72, 0.77±0.130), group D (12.89±2.58, 0.48±0.057) were significantly increased than those in group A (1.02±0.13, 0.18±0.025), and in group D they were significantly decreased than group C (all <0.01). There was no significant difference of all the above indicators between group B and C (all >0.05). MiR-146a can reduce acute lung inflammation and TLR4 expression in lungs of rats with mechanical ventilator-induced lung injury. MiR-146a may inhibit the inflammatory response through TLR4 signaling pathway.

摘要

探讨微小RNA-146a(miR-146a)对机械通气所致肺损伤大鼠肺组织中Toll样受体4(TLR4)炎症信号通路的影响及其机制。将32只健康雄性Sprague-Dawley大鼠随机分为4组(每组 = 8只):A组为正常对照组,不进行机械通气,自主呼吸;B组为机械通气损伤组;C组为机械通气损伤加空载病毒转染组;D组为机械通气损伤加病毒转染组;B、C、D组进行机械通气,呼吸频率控制为80次/分钟,潮气量为40 ml/kg,吸入氧浓度(FiO)为21%,吸呼比为1∶2,呼气末正压通气(PEEP)为0,每组每天通气4小时,连续7天以建立呼吸机诱导的肺损伤(VILI)大鼠模型。取肺组织石蜡包埋切片进行HE染色,在显微镜下观察肺组织的形态及损伤情况。测定肺组织湿干比(W/D)、炎症细胞因子白细胞介素(IL)-1β、IL-2和肿瘤坏死因子(TNF)-α的水平。采用实时荧光定量PCR检测TLR4 mRNA的表达。通过蛋白质免疫印迹法测定TLR4蛋白水平。B组(6.41±0.10,11.38±0.92)、C组(6.45±0.19,11.75±1.04)、D组(5.95±0.14,7.53±4.78)肺组织W/D及肺损伤评分均显著高于A组(4.33±0.08,0.25±0.46),且D组均显著低于C组(均P<0.01)。B组[(36.07±4.28)pg/ml,(5.02±0.63)ng/ml,(382.57±35.41)ng/ml]、C组[(35.82±5.47)pg/ml,(4.98±0.71)ng/ml,(375.13±36.95)ng/ml]、D组[(27.01±3.18)pg/ml,(3.96±0.82)ng/ml,(297.56±39.08)ng/ml]IL-1β、IL-2、TNF-α水平均显著高于A组[(21.46±3.15)pg/ml,(2.45±0.17)ng/ml,(195.92±18.07)ng/ml],且D组均显著低于C组(均P<0.01)。B组(29.57±5.10,0.75±0.110)、C组(27.27±4.72,

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