期刊文献+

大鼠颅脑损伤急性期水通道蛋白4表达变化的研究 被引量:3

Expression of AQP4 during acute stage of traumatic brain injury in rats
下载PDF
导出
摘要 目的探讨水通道蛋白4(AQP4)在大鼠重型颅脑损伤时的表达变化及其与脑水肿间的关系。方法98只成年雄性Wistar大鼠,随机分为对照组及实验组(伤后0.5、2、6、12、24、48、72 h共7组,对照组不打击)。制作大鼠液压冲击颅脑损伤模型,分别于伤后0.5、2、6、12、24、48、72 h采用干湿比重法测脑组织含水量,半定量反转录聚合酶链反应(RT-PCR)检测脑组织AQP4 mRNA表达及其变化。结果脑组织AQP4 mRNA在伤后0.5 h开始表达上调,2、6、12 h依次增高,24 h达到峰值(P<0.05),72 h时仍维持较高水平。脑组织含水量与AQP4 mRNA表达变化一致。经相关性分析,AQP4 mRNA的表达与脑组织含水量呈正相关(r=0.095,P<0.05)。结论重型脑损伤急性期,AQP4 mRNA表达变化与颅脑损伤后脑水肿的形成和发展密切相关。AQP4可能参与重型脑损伤后脑水肿的形成并起重要作用。 Objective To investigate the expression of aquaporin-4 (AQP4) and its correlation with brain edema during the acute phase of severe traumatic brain injury (TBI) in rats. Methods Fifty-six adult male Wistar rats were randomized into seven experimental groups (0.5, 2, 6, 12, 24, 48 and 72 h post-injury) and one control group. A severe TBI model generated with hydraulic impact was used. At each time spots, the water contents in the brain tissues were measured as wet-to-dry weight ratio and the expression of AQP4 mRNA was assessed by semi-quantitative RT- PCR. Results The expression of AQP4 mRNA was up-regulated 0.5 hours after injury, progressively enhanced from 2 h to 6 h to 12 h, peaked at 24 h (P〈0.05) and remained a high level at 72 h. A similar change was noted for water contents in brain tissues. Correlation analysis showed that the expression of AQP4 mRNA was positively correlated with brain water contents (r=0.095 ,P〈0.05). Conclusion The changes in AQP4 mRNA expression may be closely related to formation and progression of brain edema during the acute stage of severe traumatic brain injury. AQP4 may be playing an important role in brain edema after severe TBI.
出处 《中国药物与临床》 CAS 2008年第5期341-343,共3页 Chinese Remedies & Clinics
基金 国家自然科学基金资助项目(30600637)
关键词 脑损伤 脑水肿 水通道蛋白 Brain injury Brain edema Aquaporins
  • 相关文献

参考文献1

二级参考文献11

  • 1Kazuko Aoki,Toshiki Uchihara,Kuniaki Tsuchiya,Ayako Nakamura,Kenji Ikeda,Yoshihiro Wakayama.Enhanced expression of aquaporin 4 in human brain with infarction[J].Acta Neuropathologica.2003(2)
  • 2K Aoki,T Uchihara,K Tsuchiya,A Nakamura,K Ikeda,Y Wakayama.Enhanced expression of aquaporin 4 in human brain with infarction[].Acta Neuropathologica.2003
  • 3S Saadoun,MC Papadopoulos,DC Davies,S Krishna,BA Bell.Aquaporin-4 expression is increased in oedematous human brain tumours[].Journal of Neurology Neurosurgery and Psychiatry.2002
  • 4MC Sun,CR Honey,C Berk,NL Wong,JK Tsui.Regulation of aquaporin-4 in a traumatic brain injury model in rats[].Journal of Neurosurgery.2003
  • 5Taniguchi M,Yamashita T,Kumura E,Tamatani M,Kobayashi A,Yokawa T,Maruno M,Kato A,Ohnishi T,Kohmura E,Tohyama M,Yoshimine T.Induction of aquaporin-4 water channel mRNA after focal cerebral ischemia in rat[].Brain Research Molecular Brain Research.2000
  • 6VerkmanAS.Aquaporinwaterchannelsandendothelialcellfunction[].JAnat.2002
  • 7Ishibashi K,Kuwahara M,Gu Y,et al.Water and glycerol permeability of aquaporin 1-5 and MIP determined quantitatively by expression of epitope-tagged constructs[].Journal of Biological Chemistry.1997
  • 8Denker BM,,Smith BL,,Kuhajda FP,Agre P.Identification,purification,and partial characterization of a novel Mr28,000integral membrane protein from erythrocytes andrenal tubules[].Journal of Biological Chemistry.1988
  • 9RR Leker,E Shohami.Cerebral ischemia and trauma-different etiologies yet similar mechanisms: neuroprotective opportunities[].Brain Research.2002
  • 10GT Manley,M Fujimura,T Ma,N Noshita,F Filiz,AW Bollen,P Chan,AS Verkman.Aquaporin-4 deletion in mice reduces brain edema after acute water intoxication and ischemic stroke[].Nature Medicine.2000

共引文献18

同被引文献24

  • 1张天益,罗文新,何碧军,刘惠玉,黄育驰.复方麝香注射液联合补阳还五汤治疗重型颅脑损伤51例临床观察[J].中国中医药科技,2004,11(6):367-368. 被引量:8
  • 2Raghupathi R.Cell death mechanisms following traumatic brain injury[J].Brain Pathol,2004,14(2):215-222.
  • 3Reglodi D,Tamas A,Lengvari I.Examination of sensorimotor performance following middle cerebral artery occlusion in rats[J].Brain Res Bull,2003,59(6):459-466.
  • 4Wilson M,Montgomery H.Impact of genetic factors on outcome from brain injury[J].Br J Anaesth,2007,99(7):43-48.
  • 5Werner C,Engelhard K.Pathophysiology of traumatic brain injury[J].Br J Anaesth,2007,99:4-9.
  • 6Zhao TY,Zou SP,Alimova YV,et al.Short interfering RNAinduced gene silencing is transmitted between cells from the mammalian central nervous system[J].J Neurochem,2006,98(10):1541-1550.
  • 7Culmsee C,Gasser E,Hansen S,et al.Effects of Raf-1 siRNA on human cerebral microvascular endothelial cells:a potential therapeutic strategy for inhibition of tumor angiogenesis[J].Brain Res,2006,1125(2):147-154.
  • 8Vieira Rde C, Hora EC, Oliveira DV, et al. Quality of life of victims of traumatic brain injury six months after the trauma[ J]. Rev Lat Am Enfer- magem,2013,21 (4) :868-875.
  • 9Chung TS, Lung FW. Different impacts of aquaporin 4 and MAOA allele variation among olanzapine, risperidone, and paliperidone in schizophrenia [ J]. Clin Psychopharmaco1,2012,32 ( 3 ) :394-397.
  • 10Gavrilov K, Saltzman WM. Therapeutic siRNA : principles, challenges, and strategies [ J ]. Yale J Biol Med,2012,85 ( 2 ) : 187-200.

引证文献3

二级引证文献16

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部