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大鼠实验性脑出血后水通道蛋白4 mRNA表达与血脑屏障通透性的关系 被引量:8

The Relationship Between Aquaporin-4 mRNA Expression and Blood-Brain Barrier Permeability After Experimental Cerebral Hemorrhage in Rats
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摘要 目的 研究大鼠脑出血后水通道蛋白4mRNA表达与血脑屏障通透性的关系。方法 采用自体非抗凝动脉血注入尾状核法制作大鼠脑出血模型,逆转录聚合酶链反应法观察水通道蛋白4mRNA的表达,伊文思兰法检测血脑屏障通透性,干湿重法计算脑含水量以代表脑水肿情况。结果 与对照组比较,脑出血组水通道蛋白4mRNA表达6h即开始升高(1.06±0.12),3天时达到高峰(1.34±0.14),7天时仍高于正常组(P〈0.05);血脑屏障通透性于出血后6h开始升高(0.5955±0.0956),1天-3天最高(0.8889±0.0968、0.7914±0.0520),5天-7天逐渐降低(P〈0.05)。水通道蛋白4mRNA表达与血脑屏障通透性呈显著正相关(r=0.686,P〈0.01),与脑水肿变化趋势相一致。结论 脑出血后可能通过上调水通道蛋白4mRNA表达,增加血脑屏障通透性,参与脑水肿形成。 Aim To investigate the relafionship between aquaporin-4(AQP4)mRNA expression and blood-brain barrier (BBB) permeability after experimental cerebral hemorrhage in rats. Methods The cerebral hemorrhage models were establisbed by stereotaxic injection of auto-non-anticoagulant artery blood into the caudate nucleus. AQP4 rnRNA expression was detected by RT-PCR, BBB permeability by Evens Blue method and brain water contents by dry-wet weight method. Results In contrast to the control group, AQP4 mRNA expression increased in cerebral hemorrhage group at 6 hours ( 1.06 ± 0.12), reached peak at 3 days( 1.34 ± 0.14), then was still higher than normal at 7 days ( P〈0.05) ; BBB permeability increased at 6 hours after cerebral hemorrhage (0.5955 ± 0.0956), reached peak at 1-3 days (0.8889 ± 0.0968, 0.7914± 0.0520), and decreased at 5-7 days gradually (P〈0.05 ). There was a significantly positive correlation between AQP4 mRNA expression and BBB penncability (r=0.686, P〈0.01), whieh was comistent with the ehange of eerebral edema. Conclusion Cerebraledema may be formed through the up-regulation of aquapofin-4 mRNA expression and the increase of BBB permeability after cerebral hemorrhage.
出处 《中国动脉硬化杂志》 CAS CSCD 2006年第4期330-332,共3页 Chinese Journal of Arteriosclerosis
关键词 神经病学 脑水肿 逆转录聚合酶链反应 脑出血 水通道蛋白 血脑屏障通透性 大鼠 Cerebral Hemorrhage Aquaporin Blood-Brain Barrier Brain Edema Permeability Rat
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参考文献12

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二级参考文献24

  • 1石向群,杨金升,王运良,石莉,包仕尧.水通道蛋白4基因干预对大鼠脑缺血再灌注损伤后脑水肿的影响[J].中国临床康复,2004,8(28):6114-6116. 被引量:5
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