Jia Feng, Mao Qing, Liang Yu-Min, Jiang Ji-Yao
1 Department of Neurosurgery, Shanghai Renji Hospital, Shanghai JiaoTong University , School of Medicine, Shanghai, China .
J Neurotrauma. 2014 Feb 15;31(4):387-94. doi: 10.1089/neu.2008.0814. Epub 2012 Dec 20.
Here we investigate the effect of hypothermia on the expression of apoptosis-regulating protein TIMP-3 after fluid percussion traumatic brain injury (TBI) in rats. We began with 210 adult male Sprague-Dawley rats and randomly assigned them to three groups: TBI with hypothermia treatment (32°C), TBI with normothermia (37°C), and sham-injured controls. TBI was induced by a fluid percussion TBI device. Mild hypothermia (32°C) was achieved by partial immersion in a water bath (0°C) under general anesthesia for 4 h. The rats were killed at 4, 6, 12, 24, 48, and 72 h and 1 week after TBI. The mRNA and protein level of TIMP-3 in both the injured and uninjured hemispheres of the brains from each group were measured using RT-PCR and Western blotting. In the normothermic group, TIMP-3 levels in both the injured and uninjured hemispheres were significantly increased after TBI compared with those of sham-injured animals (p < 0.01). In contrast, post-traumatic hypothermia significantly attenuated this increase. According to the RT-PCR and Western blot analyses, the maximum mRNA levels of TIMP-3 were reduced to 60.60 ± 2.30%, 55.83 ± 1.80%, 66.03 ± 2.10%, and 64.51 ± 1.50%, respectively, of the corresponding values in the normothermic group in the injured and uninjured hemispheres (cortex and hippocampus) of the hypothermia group (p < 0.01), while the respective maximum protein levels of TIMP-3 were reduced to 57.50 ± 1.50, 52.67 ± 2.20, 60.31 ± 2.50 and 54.76 ± 1.40 (p < 0.01). Our data suggest that moderate fluid percussion brain injury significantly upregulates TIMP-3 expression, and that this increase may be suppressed by hypothermia treatment.
在此,我们研究了低温对大鼠液压冲击性脑损伤(TBI)后凋亡调节蛋白TIMP-3表达的影响。我们选用210只成年雄性Sprague-Dawley大鼠,随机将它们分为三组:低温治疗的TBI组(32°C)、常温的TBI组(37°C)和假损伤对照组。通过液压冲击性脑损伤装置诱导TBI。在全身麻醉下将大鼠部分浸入0°C水浴4小时以实现轻度低温(32°C)。在TBI后的4、6、12、24、48、72小时以及1周处死大鼠。使用逆转录聚合酶链反应(RT-PCR)和蛋白质印迹法检测每组大鼠大脑损伤半球和未损伤半球中TIMP-3的mRNA和蛋白质水平。在常温组中,与假损伤动物相比,TBI后损伤半球和未损伤半球中的TIMP-3水平均显著升高(p < 0.01)。相比之下,创伤后低温显著减弱了这种升高。根据RT-PCR和蛋白质印迹分析,低温组损伤半球和未损伤半球(皮质和海马)中TIMP-3的最大mRNA水平分别降至常温组相应值的60.60±2.30%、55.83±1.80%、66.03±2.10%和64.51±1.50%(p < 0.01),而TIMP-3各自的最大蛋白质水平分别降至57.50±1.50、52.67±2.20、60.31±2.50和54.76±1.40(p < 0.01)。我们的数据表明,中度液压冲击性脑损伤显著上调TIMP-3表达,并且这种增加可能被低温治疗所抑制。