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作 者:刘钢[1,2] 宋耀宗[2] 于晨[2] 刘佳[2] 孙天胜[2]
机构地区:[1]解放军医学院,北京100853 [2]北京军区总医院骨科,北京100700
出 处:《医学综述》2014年第7期1280-1282,共3页Medical Recapitulate
基 金:军队临床高新技术重大项目(2010jxjs007)
摘 要:目的探讨大鼠股骨干骨折合并脑损伤后对肺脏表面活性蛋白A(SP-A)与炎性介质的影响。方法将108只SD雄性大鼠采用随机数字表法分为空白对照组(12只)、股骨干骨折组(32只)、脑损伤组(32只)、股骨干骨折合并脑损伤组(32只)。各组分别于1、6、12、24 h取材,取材部位为右肺下叶,应用Western Blot检测肺组织SP-A表达,酶联免疫吸附测定法检测肺组织中肿瘤坏死因子α(TNF-α)、白细胞介素(IL)6、IL-10的水平。结果 6 h时骨折组、脑损伤组、骨折合并脑损伤组SP-A水平均升高,24 h时骨折合并脑损伤组SP-A降至对照组以下(P<0.05)。创伤后肺脏TNF-α、IL-6、IL-10均升高,骨折组、脑损伤组、骨折合并脑损伤组TNF-α、IL-6、IL-10水平均高于对照组(P<0.05),且骨折合并脑损伤组最高,与骨折组、脑损伤组比较差异统计学意义(P<0.05)。结论创伤后肺脏组织炎性介质及SP-A水平发生变化,与创伤程度密切相关。较轻的创伤会出现炎性介质升高,SP-A代偿性升高,严重创伤时SP-A失代偿性下降。Objective To study the influence of rat femoral fractures combined with traumatic brain injury on inflammatory mediator and SP-A in lungs. Methods Sprague-Dawley rats were randomly divided into 4 groups : control group ( n = 12 ), closed femoral fracture group ( n = 32 ), traumatic brain injury group (n = 32), closed femoral fracture combined with traumatic brain injury( n = 32). Got the part of the inferior lobe of right lung tissue at 1,6,12,24 h after modeling, Western Blot was employed to detect SP-A. Then levels of TNF-α,IL-6,IL-10 were dected with ELISA. Results The SP-A levels of three experiment groups increased compared with control group at 6 h. At 24 h SP-A of femoral fracture combined with traumatic brain injury group dropped below control group ( P 〈 0.05 ). Trauma can improve the levels of TNF-α, IL-6, IL-10, three experiment groups had statistical significant difference compared with control group ( P 〈 0.05 ) and femoral fracture combined with traumatic brain injury group was the highest with statistically significant difference from the closed femoral fracture group and traumatic brand injury group( P 〈 0.05 ). Conclusion The level of inflammatory mediator and SP-A change after injury, and are closely related to the degree of trauma. Minor injury may increase the level of inflammatory mediator and SP-A, while trauma can decrease SP-A when uncompensated.
分 类 号:R332[医药卫生—人体生理学]
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