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9.4 T下TX模型小鼠脑组织的扩散张量成像研究 被引量:3

Diffusion Tensor Imaging on TX Mice Brain at 9.4 T
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摘要 本文首次应用9.4T高场磁共振扩散张量成像(diffusion tensor imaging,DTI)技术,研究了Wilson疾病模型TX(toxic milk)小鼠的脑组织微观结构改变和结构连接情况.基于感兴趣区域(region of interest,ROI)的分析发现,与对照组相比,TX模型组的各向异性比值(fractional anisotropy,FA)在海马、尾状核和苍白球显著下降;平均扩散率(mean diffusivity,MD)则呈现上升趋势,但无统计学意义.纤维束追踪法结果表明TX模型组小鼠的脑结构连接并未受到严重破坏,证明了铜累积对脑组织的损伤具有区域性. Diffusion tensor imaging(DTI)was used to evaluate micro-structural changes and structural connectivity in the TX mice model of Wilson’s disease(WD)at 9.4 T.Region of interest(ROI)analysis showed that mean fractional anisotropy(FA)values in the hippocampus,caudate putamen and lateral globus pallidus of the TX mice decreased significantly,relative to those in the control mice.The mean diffusivity(MD)values in these regions showed no significant inter-group differences.The results of fiber tracking demonstrated that structural connectivity of in the brain of TX mice was maintained,indicating that the effects of copper accumulation in these mice were mainly regional.
作者 鲁晨 董健健 钟凯 LU Chen;DONG Jian-jian;ZHONG Kai(High Magnetic Field Laboratory,Chinese Academy of Sciences,Hefei 230031,China;University of Science and Technology of China,Hefei 230026,China)
出处 《波谱学杂志》 CAS 北大核心 2019年第4期510-516,共7页 Chinese Journal of Magnetic Resonance
基金 国家自然科学基金重大研究计划(91649101) 中科院合肥大科学中心重点研发项目(2017HSC-KPRD003)
关键词 9.4 T 扩散张量成像(DTI) TX模型小鼠 各向异性比值 平均扩散率 9.4 T diffusion tensor imaging(DTI) TX mice fractional anisotropy mean diffusivity
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  • 1李兴华,徐云虹,许爱芳,龚燕芳,屠振兴,李兆申.自发性肝癌的LEC大鼠的GST-P异常表达和p53基因突变[J].第二军医大学学报,2005,26(1):113-115. 被引量:4
  • 2陈曦,梁秀龄,汤其强,丰岩清,石铸,陈松林,黎锦如.1~6月龄TX小鼠铜代谢和肝损害情况研究[J].中山大学学报(医学科学版),2005,26(3):253-256. 被引量:14
  • 3石元洪,洪永春,杨任民,胡纪源.肝细胞体外培养对肝豆汤排铜作用的拆方研究[J].陕西中医,2006,27(9):1145-1147. 被引量:6
  • 4Sudmeyer M, Saleh A, Wojtecki L, et al. Wojtecki, et al. Wilsons disease tremor is associated with magnetic resonance imaging lesions in basal ganglia structures[J]. Mov Disord, 2006, 21(12): 2134- 2139.
  • 5N awaz M, Manzi C, Lacher V, et al. Copper-induced stimulation of extracellular signal-regulated kinase in trout hepatooytes ? the role of reactive oxygen species, Ca2 + , and cell energetics and the impact of extracellular signal-regulated kinase signaling on apoptosis and nee?rosis[J]. Toxicol Sci, 2006, 92(2): 464 -475.
  • 6SulpiceJC, Zachowski A, Devaux PF, et al. Requirement for phos?phatidylinositol 4 ,5-bisphosphate in the Ca(2 + ) -induced phospho?lipid redistribution in the human erythrocyte membrane[J].J Bioi Chern, 1994,269(9): 6347 -6354.
  • 7VanlandinghamJW, Tassabehji NM, Somers RC, et al. Expression profiling of p53 -target genes in copper-mediated neuronal apoptosis[J]. Neuromolecular Med, 2005, 7 (4) : 311 - 324.
  • 8Tassabehji NM, VanLandinghamJW, Levenson CWo Copper alters the conformation and transcriptional activity of the tumor suppressor protein p53 in human Hep G2 cells[J]. Exp Bioi Med (May?wood), 2005, 230( I(): 699 -708.
  • 9Mufti AR, Burstein E, Csomos RA, et al. XIAP is a copper binding protein deregulated in Wilsons disease and other copper toxicosis disordersj]]. Mol Cell, 2006, 21(6): 775 -785.
  • 10Mufti A R, Burstein E, Duckett CS. XIAP: cell death regulation meets copper homeostasis[J]. Arch Biochem Biophys, 2007, 463 (2): 168-174.

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