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本文引用的文献

1
Differential behavioral and histopathological responses to graded cortical impact injury in mice.小鼠对分级皮质撞击损伤的行为和组织病理学差异反应。
J Neurotrauma. 2006 Aug;23(8):1241-53. doi: 10.1089/neu.2006.23.1241.
2
Spatiotemporal evolution of apoptotic neurodegeneration following traumatic injury to the developing rat brain.发育中大鼠脑创伤后凋亡性神经变性的时空演变
Brain Res. 2006 Aug 30;1107(1):70-81. doi: 10.1016/j.brainres.2006.05.102. Epub 2006 Jul 5.
3
Traumatic brain injury in mice deficient in Bid: effects on histopathology and functional outcome.Bid基因缺陷小鼠的创伤性脑损伤:对组织病理学和功能结果的影响。
J Cereb Blood Flow Metab. 2006 May;26(5):625-33. doi: 10.1038/sj.jcbfm.9600258.
4
All roads lead to disconnection?--Traumatic axonal injury revisited.条条大路通“失联”?——再探创伤性轴突损伤
Acta Neurochir (Wien). 2006 Feb;148(2):181-93; discussion 193-4. doi: 10.1007/s00701-005-0674-4. Epub 2005 Dec 20.
5
Selective temporal and regional alterations of Nogo-A and small proline-rich repeat protein 1A (SPRR1A) but not Nogo-66 receptor (NgR) occur following traumatic brain injury in the rat.大鼠创伤性脑损伤后,Nogo-A和富含脯氨酸的小重复蛋白1A(SPRR1A)出现选择性的时间和区域改变,但Nogo-66受体(NgR)未出现这种改变。
Exp Neurol. 2006 Jan;197(1):70-83. doi: 10.1016/j.expneurol.2005.08.029.
6
Morris water maze search strategy analysis in PDAPP mice before and after experimental traumatic brain injury.实验性创伤性脑损伤前后PDAPP小鼠的莫里斯水迷宫搜索策略分析
Exp Neurol. 2006 Feb;197(2):330-40. doi: 10.1016/j.expneurol.2005.10.020. Epub 2005 Nov 23.
7
Caspase inhibition therapy abolishes brain trauma-induced increases in Abeta peptide: implications for clinical outcome.半胱天冬酶抑制疗法可消除脑外伤引起的β淀粉样肽增加:对临床结果的影响。
Exp Neurol. 2006 Feb;197(2):437-50. doi: 10.1016/j.expneurol.2005.10.011. Epub 2005 Nov 21.
8
Administration of the immunophilin ligand FK506 differentially attenuates neurofilament compaction and impaired axonal transport in injured axons following diffuse traumatic brain injury.亲免素配体FK506的给药可不同程度地减轻弥漫性创伤性脑损伤后受损轴突中的神经丝压缩和轴突运输受损。
Exp Neurol. 2006 Feb;197(2):353-62. doi: 10.1016/j.expneurol.2005.10.003. Epub 2005 Nov 17.
9
Experimental models of traumatic brain injury: do we really need to build a better mousetrap?创伤性脑损伤的实验模型:我们真的需要制造一个更好的捕鼠器吗?
Neuroscience. 2005;136(4):971-89. doi: 10.1016/j.neuroscience.2005.08.030. Epub 2005 Oct 20.
10
Age-dependent reduction of cortical contusion volume by ketones after traumatic brain injury.创伤性脑损伤后酮类物质对皮质挫伤体积的年龄依赖性减少作用。
J Neurosci Res. 2005 Nov 1;82(3):413-20. doi: 10.1002/jnr.20633.

用于精确、分级实验性创伤性脑损伤的电磁控制皮质撞击装置。

Electromagnetic controlled cortical impact device for precise, graded experimental traumatic brain injury.

作者信息

Brody David L, Mac Donald Christine, Kessens Chad C, Yuede Carla, Parsadanian Maia, Spinner Mike, Kim Eddie, Schwetye Katherine E, Holtzman David M, Bayly Philip V

机构信息

Department of Neurology, Hope Center for Neurological Disorders, Washington University, St. Louis, Missouri, USA.

出版信息

J Neurotrauma. 2007 Apr;24(4):657-73. doi: 10.1089/neu.2006.0011.

DOI:10.1089/neu.2006.0011
PMID:17439349
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2435168/
Abstract

Genetically modified mice represent useful tools for traumatic brain injury (TBI) research and attractive preclinical models for the development of novel therapeutics. Experimental methods that minimize the number of mice needed may increase the pace of discovery. With this in mind, we developed and characterized a prototype electromagnetic (EM) controlled cortical impact device along with refined surgical and behavioral testing techniques. By varying the depth of impact between 1.0 and 3.0 mm, we found that the EM device was capable of producing a broad range of injury severities. Histologically, 2.0-mm impact depth injuries produced by the EM device were similar to 1.0-mm impact depth injuries produced by a commercially available pneumatic device. Behaviorally, 2.0-, 2.5-, and 3.0-mm impacts impaired hidden platform and probe trial water maze performance, whereas 1.5-mm impacts did not. Rotorod and visible platform water maze deficits were also found following 2.5- and 3.0-mm impacts. No impairment of conditioned fear performance was detected. No differences were found between sexes of mice. Inter-operator reliability was very good. Behaviorally, we found that we could statistically distinguish between injury depths differing by 0.5 mm using 12 mice per group and between injury depths differing by 1.0 mm with 7-8 mice per group. Thus, the EM impactor and refined surgical and behavioral testing techniques may offer a reliable and convenient framework for preclinical TBI research involving mice.

摘要

转基因小鼠是创伤性脑损伤(TBI)研究的有用工具,也是开发新型治疗方法颇具吸引力的临床前模型。尽量减少所需小鼠数量的实验方法可能会加快发现的速度。考虑到这一点,我们开发并表征了一种原型电磁(EM)控制的皮质撞击装置以及完善的手术和行为测试技术。通过将撞击深度在1.0至3.0毫米之间变化,我们发现该电磁装置能够产生广泛的损伤严重程度。组织学上,电磁装置产生的2.0毫米撞击深度损伤与市售气动装置产生的1.0毫米撞击深度损伤相似。行为学上,2.0、2.5和3.0毫米的撞击会损害隐藏平台和探针试验水迷宫的表现,而1.5毫米的撞击则不会。在2.5和3.0毫米撞击后,还发现了转棒试验和可见平台水迷宫缺陷。未检测到条件性恐惧表现受损。未发现小鼠性别之间存在差异。不同操作人员之间的可靠性非常好。行为学上,我们发现每组使用12只小鼠时,我们可以在统计学上区分相差0.5毫米的损伤深度,每组使用7 - 8只小鼠时,可以区分相差1.0毫米的损伤深度。因此,电磁撞击器以及完善的手术和行为测试技术可能为涉及小鼠的临床前TBI研究提供一个可靠且方便的框架。