期刊文献+

大鼠创伤性轴索损伤后脑代谢质子磁共振波谱分析 被引量:5

Proton magnetic resonance spectroscopy of brain metabolism after traumatic axonal injury in rats
原文传递
导出
摘要 目的使用质子磁共振波谱(^1H—MRS)研究大鼠创伤性轴索损伤(traumatic axonal injury,TAI)后组织代谢改变及其空间分布特征。方法使大鼠头颅发生线加速和角加速运动制作TAI模型。于伤前和伤后24h采用多体素MRS方法检测大鼠脑内多个部位的组织代谢状态,分析伤后N-乙酰门冬氨酸(NAA)/总肌酸(Cr)、NAA/胆碱类化合物(Cho)和Cho/Cr值变化及NAA/Cr值变化的空间分布特征。采用免疫组化标记β淀粉样蛋白前体蛋白(p—APP)观察轴索损伤情况。结果与伤前相比,伤后24h时NAA/Cr、NAA/Cho值显著下降(P〈0.05),Cho/Cr值轻度升高(P〉0.05);NAA/Cr值出现较大降低幅度的部位依次为脑干、海马、内囊、胼胝体和丘脑。病理学检查示这些部位出现轴索损伤。结论TAI后脑组织出现严重代谢紊乱,以脑干、海马等部位变化最为显著。 Objective To investigate the brain metabolic changes and evaluate their spatial distributions after traumatic axonal injury ( TAI ) in rats by using proton magnetic resonance spectroscopy (IH-MRS). Methods The TAI model was made by subjecting the head of the rats to the linear and angular accelerations. The multi-voxel MRS was employed to detect the tissue metabolic state at the levels of hippocampus-caudate and pons prior to injury and at 24 hours after injury. The alterations of NAA/Cr, NAA/Cho and Cho/Cr values as well as the spatial distribution of NAA/Cr reduction were accessed, hnmunohistochemical staining for β-APP was used to observe the injured axons. Results A significant decrease in NAA/Cr and NAA/Cho ( P 〈 0.05) and subtle increase in Cho/Cr (P 〉 0.05 ) were observed in rats at 24 hours after TAI in comparison to the pre-injury levels. Notable decrease in NAA/Cr value was observed in the areas including the brain stem, hippocampus, internal capsule, corpus callosum and thalamus, where axonal injuries were confirmed by the histological examination. Conclusion Metabolic imbalances occur in the brains of rats with TAI, with notable changes in the brain stem and the hippocampus.
出处 《中华创伤杂志》 CAS CSCD 北大核心 2011年第3期213-217,共5页 Chinese Journal of Trauma
基金 上海市科委攻关计划资助项目(064119639) 上海交通大学医学院基金资助项目(09XJ21072) 上海交通大学医工结合专项资助项目(YG08PETMS19)
关键词 弥漫性轴索损伤 磁共振波谱 代谢 Diffuse axonal injury Magnetic resonance spectroscopy Metabolism Brain
  • 相关文献

参考文献15

  • 1Li XY, Feng DF. Diffuse axonal injury: novel insights into detec- tion and treatment. J Clin Neurosci, 2009, 16(5) :614-619.
  • 2Pascual JM, Solivera J, Prieto R, et al. Time course of early metabolic changes following diffuse traumatic brain injury in rats as detected by IH NMR spectroscopy. J Neurotrauma, 2007, 24(6): 944 - 959.
  • 3李雪元,戴广辉,冯东福,李甲,顾磊.小动物弥漫性脑损伤致伤装置的设计[J].生物医学工程与临床,2009,13(6):489-493. 被引量:2
  • 4I,i XY, l.i J, Feng DF, et al. Diffuse axonal injury induced by simultaneous moderate linear and angular head accelerations in rats. Neuroscience, 2010, 169( 1 ) :357 -369.
  • 5PaxinosG,WatsonC.大鼠脑立体定向图谱.诸葛启钏.瞿佳,程刚,等泽.第3版.北京:人民卫生出版社,2005:94-142.
  • 6Pendlebury ST, Blamire AM, Lee MA, et al. Axonal injury in the internal capsule correlates with motor impairmenl after stroke. Stroke, 1999, 30(5) :956 -962.
  • 7Xu J, Rasmussen IA, l,agopoulos J, et al. Diffuse axonal injury, in severe traumatic: brain injury visualized using high - resolution diffusion tensor imaging. J Neurotrauma. 2007, 24(5 ) :753 -765.
  • 8Marino S, Zei E, Battaglini M, et al. Acute metabolic brain changes following traumatic brain injury and their relevance to clinical severity and outeome. J Neurol Neurosurg Psyehiatry, 2007, 78 (5) :501 -507.
  • 9Smith DH, Meaney DF, Shull WH. Diffuse axonal injury in head trauma. J Head Trauma Rehabil, 2003, 18 (4) :307 - 316.
  • 10Signoretti S, Marmarou A, Tavazzi B, et al. N - Acetylaspartate reduction as a measure of injury severity and mitochondrial dysfunction following diffuse traumatic brain injury. J Neurotrauma, 2001, 18(10) :977 -991.

二级参考文献41

  • 1王正国,李磊,刘良明,梁华平,蒋建新.我国战创伤基础研究进展[J].中华创伤杂志,1996,12(5):273-275. 被引量:15
  • 2Rosen Y, Lenkinski RE. Recent advances in magnetic resonance neurospectroscopy [ J]. Neurotherapeutics, 2007, 4 (3) : 530 - 345.
  • 3Hillary FG, Liu WC, Genova HM, et al. Examining lactate in severe TBI using proton magnetic resonance spectroscopy [ J ]. Brain Inj, 2007, 21(9) : 981 -991.
  • 4Shutter L, Tong KA, Lee A, et al. Prognostic role of proton magnetic resonance spectroscopy in acute traumatic brain injury [ J ]. J Head Trauma Rehabil, 2006, 21 (4) : 334 - 349.
  • 5Signoretti S, Marmarou A, Tavazzi B, et al. N-Acetylaspartate reduction as a measure of injury severity and mitochondrial dysfunction following diffuse traumatic brain injury [ J].J Neurotrauma, 2001, 18 (10) : 977 -991.
  • 6Garnett MR, Blamire AM, Rajagopalan B, et al. Evidence for cellular damage in normal-appearing white matter correlates with injury severity in patients following traumatic brain injury: A magnetic resonance spectroscopy study [ J]. Brain, 2000, 123 ( Pt 7) : 1403 - 1409.
  • 7Govindaraju V, Gauger GE, Manley GT, et al. Volumetric proton spectroscopic imaging of mild traumatic brain injury [ J ]. AJNR Am J Neuroradiol, 2004, 25 (5) : 730 - 737.
  • 8Ashwal S, Babikian T, Gardner-Nichols J, et al. Susceptibilityweighted imaging and proton magnetic resonance spectroscopy in assessment outcome after pediatric traumatic brain injury [ J ]. Arch Phys Med Rehabil, 2006, 87( 12 Suppl 2) : 50 -58.
  • 9Holshouser BA, Tong KA, Ashwal S. Proton MR spectroscopic imaging depicts diffuse axonal injury in children with traumatic brain injury [J]. AJNR Am J Neuroradiol, 2005, 26(5) : 1276 -1285.
  • 10Shutter L, Tong KA, Holshouser BA. Proton MRS in acute traumatic brain injury: role for glutamate/glutamine and choline for outcome prediction [J]. J Neurotrauma, 2004, 21 (12) : 1693 - 1705.

共引文献23

同被引文献46

引证文献5

二级引证文献11

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