• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

可控皮质撞击所致创伤性脑损伤后的认知缺陷

Cognitive deficits following traumatic brain injury produced by controlled cortical impact.

作者信息

Hamm R J, Dixon C E, Gbadebo D M, Singha A K, Jenkins L W, Lyeth B G, Hayes R L

机构信息

Department of Psychology, Virginia Commonwealth University, Richmond.

出版信息

J Neurotrauma. 1992 Spring;9(1):11-20. doi: 10.1089/neu.1992.9.11.

DOI:10.1089/neu.1992.9.11
PMID:1619672
Abstract

Traumatic brain injury produces significant cognitive deficits in humans. This experiment used a controlled cortical impact model of experimental brain injury to examine the effects of brain injury on spatial learning and memory using the Morris water maze task. Rats (n = 8) were injured at a moderate level of cortical impact injury (6 m/sec, 1.5-2.0 mm deformation). Eight additional rats served as a sham-injured control group. Morris water maze performance was assessed on days 11-15 and 30-34 following injury. Results revealed that brain-injured rats exhibited significant deficits (p less than 0.05) in maze performance at both testing intervals. Since the Morris water maze task is particularly sensitive to hippocampal dysfunction, the results of the present experiment support the hypothesis that the hippocampus is preferentially vulnerable to damage following traumatic brain injury. These results demonstrate that controlled cortical impact brain injury produces enduring cognitive deficits analogous to those observed after human brain injury.

摘要

创伤性脑损伤会给人类带来显著的认知缺陷。本实验采用实验性脑损伤的控制性皮质撞击模型,利用莫里斯水迷宫任务来研究脑损伤对空间学习和记忆的影响。大鼠(n = 8)接受中等程度的皮质撞击损伤(6米/秒,1.5 - 2.0毫米变形)。另外8只大鼠作为假损伤对照组。在损伤后的第11 - 15天和第30 - 34天评估莫里斯水迷宫表现。结果显示,在两个测试时间段,脑损伤大鼠在迷宫表现上均出现显著缺陷(p小于0.05)。由于莫里斯水迷宫任务对海马功能障碍特别敏感,本实验结果支持以下假说:创伤性脑损伤后,海马特别容易受到损伤。这些结果表明,控制性皮质撞击脑损伤会产生类似于人类脑损伤后观察到的持久认知缺陷。

相似文献

1
Cognitive deficits following traumatic brain injury produced by controlled cortical impact.可控皮质撞击所致创伤性脑损伤后的认知缺陷
J Neurotrauma. 1992 Spring;9(1):11-20. doi: 10.1089/neu.1992.9.11.
2
Attenuation of working memory and spatial acquisition deficits after a delayed and chronic bromocriptine treatment regimen in rats subjected to traumatic brain injury by controlled cortical impact.在通过控制性皮质撞击造成创伤性脑损伤的大鼠中,采用延迟和慢性溴隐亭治疗方案后,工作记忆和空间学习能力缺陷的减轻。
J Neurotrauma. 2002 Apr;19(4):415-25. doi: 10.1089/08977150252932370.
3
Increased anticholinergic sensitivity following closed skull impact and controlled cortical impact traumatic brain injury in the rat.大鼠闭合性颅骨撞击和控制性皮质撞击性脑损伤后抗胆碱能敏感性增加。
J Neurotrauma. 1994 Jun;11(3):275-87. doi: 10.1089/neu.1994.11.275.
4
One-year study of spatial memory performance, brain morphology, and cholinergic markers after moderate controlled cortical impact in rats.大鼠中度控制性皮质撞击后空间记忆表现、脑形态学及胆碱能标志物的一年研究。
J Neurotrauma. 1999 Feb;16(2):109-22. doi: 10.1089/neu.1999.16.109.
5
Morris water maze deficits in rats following traumatic brain injury: lateral controlled cortical impact.创伤性脑损伤后大鼠的莫里斯水迷宫缺陷:侧方控制性皮质撞击
J Neurotrauma. 1997 Sep;14(9):615-27. doi: 10.1089/neu.1997.14.615.
6
Delayed neuromotor recovery and increased memory acquisition dysfunction following experimental brain trauma in mice lacking the DNA repair gene XPA.实验性颅脑创伤后缺乏 DNA 修复基因 XPA 的小鼠出现神经运动恢复延迟和记忆获得功能障碍增加。
J Neurosurg. 2012 Jun;116(6):1368-78. doi: 10.3171/2012.2.JNS11888. Epub 2012 Mar 30.
7
A semicircular controlled cortical impact produces long-term motor and cognitive dysfunction that correlates well with damage to both the sensorimotor cortex and hippocampus.半圆形控制皮质撞击会产生长期的运动和认知功能障碍,这与感觉运动皮层和海马体的损伤密切相关。
Brain Res. 2014 Aug 12;1576:18-26. doi: 10.1016/j.brainres.2014.05.042. Epub 2014 Jun 4.
8
Dissociable long-term cognitive deficits after frontal versus sensorimotor cortical contusions.额叶与感觉运动皮层挫伤后可分离的长期认知缺陷。
J Neurotrauma. 1998 Mar;15(3):199-216. doi: 10.1089/neu.1998.15.199.
9
Time course of increased vulnerability of cholinergic neurotransmission following traumatic brain injury in the rat.大鼠创伤性脑损伤后胆碱能神经传递易损性增加的时间进程。
Behav Brain Res. 1995 Oct;70(2):125-31. doi: 10.1016/0166-4328(95)80002-6.
10
Selective cognitive impairment following traumatic brain injury in rats.
Behav Brain Res. 1993 Dec 31;59(1-2):169-73. doi: 10.1016/0166-4328(93)90164-l.

引用本文的文献

1
Aminophylline targets miR-128-3p/Slc7a11 axis to attenuate neuronal ferroptosis after traumatic brain injury.氨茶碱靶向miR-128-3p/Slc7a11轴以减轻创伤性脑损伤后的神经元铁死亡。
Cell Mol Life Sci. 2025 Feb 22;82(1):87. doi: 10.1007/s00018-025-05601-3.
2
Mitochondrial-targeted therapies in traumatic brain injury: From bench to bedside.创伤性脑损伤的线粒体靶向治疗:从实验台到病床边
Neurotherapeutics. 2025 Jan;22(1):e00515. doi: 10.1016/j.neurot.2024.e00515. Epub 2024 Dec 24.
3
Viral-mediated increased hippocampal neurogranin modulate synapses at one month in a rat model of controlled cortical impact.
病毒介导的海马神经颗粒蛋白增加调节控制皮质撞击大鼠模型中一个月时的突触。
Sci Rep. 2024 Nov 22;14(1):28998. doi: 10.1038/s41598-024-77682-2.
4
Priorities for quality of life after traumatic brain injury.创伤性脑损伤后的生活质量优先事项。
PLoS One. 2024 Jul 5;19(7):e0306524. doi: 10.1371/journal.pone.0306524. eCollection 2024.
5
Reactive gliosis in traumatic brain injury: a comprehensive review.创伤性脑损伤中的反应性胶质增生:综述
Front Cell Neurosci. 2024 Feb 28;18:1335849. doi: 10.3389/fncel.2024.1335849. eCollection 2024.
6
Insights from Rodent Models for Improving Bench-to-Bedside Translation in Traumatic Brain Injury.啮齿动物模型在创伤性脑损伤中改善从基础到临床转化的研究进展。
Methods Mol Biol. 2024;2761:599-622. doi: 10.1007/978-1-0716-3662-6_40.
7
A novel hydro-pneumatic fluid percussion device for inducing traumatic brain injury: assessment of sensory, motor, cognitive, molecular, and morphological outcomes in rodents.一种用于诱导创伤性脑损伤的新型液压气动流体冲击装置:对啮齿动物感觉、运动、认知、分子和形态学结果的评估
Front Mol Neurosci. 2024 Jan 16;16:1208954. doi: 10.3389/fnmol.2023.1208954. eCollection 2023.
8
Overexpress miR-132 in the Brain Parenchyma by a Non-invasive Way Improves Tissue Repairment and Releases Memory Impairment After Traumatic Brain Injury.通过非侵入性方法在脑组织中过表达 miR-132 可改善创伤性脑损伤后的组织修复并缓解记忆损伤。
Cell Mol Neurobiol. 2023 Dec 17;44(1):5. doi: 10.1007/s10571-023-01435-4.
9
Proteomic association with age-dependent sex differences in Wisconsin Card Sorting Test performance in healthy Thai subjects.蛋白质组学与健康泰国受试者威斯康星卡片分类测试表现中年龄相关的性别差异的关联。
Sci Rep. 2023 Nov 19;13(1):20238. doi: 10.1038/s41598-023-46750-4.
10
Optogenetic Stimulation of CA1 Pyramidal Neurons at Theta Enhances Recognition Memory in Brain Injured Animals.光遗传刺激 CA1 锥体神经元在 theta 节律增强脑损伤动物的识别记忆。
J Neurotrauma. 2023 Nov;40(21-22):2442-2448. doi: 10.1089/neu.2023.0078. Epub 2023 Aug 23.