基质金属蛋白酶-9在大鼠重度脑创伤中的表达及意义  

Expression of Matrix metalloproteinase-9 in Rats after Severe Traumatic Brain Injury and Its significance

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作  者:李玉斌[1] 刘运生[2] 杨丽敏[1] 冯继[1] 徐立新[2] 罗超[2] 赵贤军[2] 

机构地区:[1]河北省秦皇岛市第一医院神经外科,河北秦皇岛066000 [2]中南大学湘雅医院,湖南长沙410008

出  处:《医学临床研究》2009年第1期23-25,共3页Journal of Clinical Research

摘  要:【目的】研究大鼠重度脑创伤后脑组织基质金属蛋白酶-9(matrix metalloproteinase,MMP-9)mRNA的表达,探讨其在脑创伤中的作用。【方法160只健康成年SD大鼠随机分为假手术组和脑创伤组,每组又按处死时间点即伤后4h、1d、3d、5d和7d分为五个亚组,每亚组6只。取伤区脑组织用干湿重法测含水量、反转录聚合酶链式反应(RT—PCR)法测MMP-9mRNA和电镜检查。【结果】大鼠重度脑创伤后脑组织含水量和MMP-9mRNA在伤后4h开始升高,1d达高峰,持续至3d,然后下降,7d达最低;除7d外脑组织含水量和MMP-9mRNA均明显高于假手术组,差异有统计学意义(P〈0.05)。【结论】大鼠重度脑创伤诱导MMP-9mRNA表达,MMP-9可能参与了脑水肿的形成,在脑创伤后继发性脑损伤中起重要作用。[Objective] To study the expression of matrix metalloproteinase-9 ( MMP-9)mRNA in brain tissue of rats after severe traumatic brain injury(TBI) and to discuss the effect of MMP-9 in severe TBI. [Methods] Sixty healthy adult Sprague-Dawley rats were randomly divided into two groups: sham operation group (SO group) and severe TBI group. The subjects were sacrificed at 4h, and 1, 3, 5, 7 days. Groups were divided into five subgroups according to the five time points ( n = 6 in each subgroup). The samples of injured brain tissue were collected to detect the content of water by dry-net method, the expression of MMP-9 mRNA was detected by RT-PCR, and the ultrastructural studies were examined by electric microscope. [Re- sults] The content of water and expression of MMP-9 mRNA in brain tissue increased at 4h, the peak value appeared at 1~3d after severe TBI, declined at 5d, with a minimum observed at 7d. In TBI group, the content of water and expression of MMP-9 mRNA in injured brain tissue were significantly higher than those in SO group at 4h, ld, 3d and 5d after severe TBI ( P d0.05). [Conclusions] The expression of MMP-9 mRNA can be induced to increase after severe TBI in rats. It is strongly suggested that MMP-9 may participate in the traumatic brain edema and play an important rol in secondary brain injury after TBI.

关 键 词:脑损伤/病理学 金属蛋白酶类 大鼠 

分 类 号:R651.15[医药卫生—外科学]

 

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