• 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

大鼠半皮质切除术后补偿性皮质脊髓投射的逆行示踪研究。

A retrograde tracing study of compensatory corticospinal projections in rats with neonatal hemidecortication.

机构信息

Department of Neuroanatomy, Yokohama City University Graduate School of Medicine, Yokohama, Japan.

出版信息

Dev Neurosci. 2011;33(6):539-47. doi: 10.1159/000335526. Epub 2012 Jan 27.

DOI:10.1159/000335526
PMID:22286753
Abstract

To examine the compensatory mechanisms in rats that underwent left decortication at postnatal day 7 (P7), we injected the retrograde tracers fluorescein isothiocyanate-cholera toxin B subunit (FITC-CTB) and Fast Blue (FB) into the right and left upper cervical spinal cord, respectively, at postoperative weeks 2, 3, 4, and 5 and counted the number of retrogradely labeled corticospinal neurons in the right cerebral cortex compared with that in normally developed rats. Significantly more ipsilaterally projecting neurons were labeled with FITC-CTB in the decorticated rats compared with normal rats at all time points examined. The number of labeled neurons was similar to that at P7 in normal rats. There were also some FITC-CTB and FB double-labeled neurons in both decorticated and normal rats. The number of double-labeled neurons in the decorticated rats increased each week and was significantly greater than that in normal rats at postoperative weeks 4 and 5. The present results suggest that the elimination of ipsilaterally projecting axons observed in normal rats was prevented in the decorticated rats, so that the cerebral cortex neurons on the unlesioned side projected corticospinal tracts to the ipsilateral spinal cord. Furthermore, the collaterals of the corticospinal tracts originating from the cerebral cortex on the unlesioned side also project to the ipsilateral spinal cord. These compensatory mechanisms might underlie the acquisition of motor function in these animals.

摘要

为了研究出生后 7 天(P7)接受左侧大脑皮层切除术的大鼠的代偿机制,我们分别在术后 2、3、4 和 5 周将逆行示踪剂荧光素异硫氰酸酯-霍乱毒素 B 亚基(FITC-CTB)和 Fast Blue(FB)注入右侧和左侧颈脊髓,并计算右侧大脑皮层中逆行标记的皮质脊髓神经元数量与正常发育大鼠相比。与正常大鼠相比,在所有检查的时间点,接受去皮质大鼠的同侧投射神经元用 FITC-CTB 标记的数量明显更多。标记神经元的数量与正常大鼠的 P7 相似。在去皮质和正常大鼠中也有一些 FITC-CTB 和 FB 双标记神经元。去皮质大鼠的双标记神经元数量每周增加,术后 4 周和 5 周明显高于正常大鼠。这些结果表明,在去皮质大鼠中,正常大鼠观察到的同侧投射轴突的消除被阻止,因此,未受损侧大脑皮层的神经元投射皮质脊髓束到同侧脊髓。此外,源自未受损侧大脑皮层的皮质脊髓束的侧支也投射到同侧脊髓。这些代偿机制可能是这些动物获得运动功能的基础。

相似文献

1
A retrograde tracing study of compensatory corticospinal projections in rats with neonatal hemidecortication.大鼠半皮质切除术后补偿性皮质脊髓投射的逆行示踪研究。
Dev Neurosci. 2011;33(6):539-47. doi: 10.1159/000335526. Epub 2012 Jan 27.
2
Differential contributions of rostral and caudal frontal forelimb areas to compensatory process after neonatal hemidecortication in rats.大鼠大脑皮质损伤后,额前肢区域的头侧和尾侧对补偿过程的不同贡献。
Eur J Neurosci. 2011 Nov;34(9):1453-60. doi: 10.1111/j.1460-9568.2011.07866.x.
3
Extension and regeneration of corticospinal axons after early spinal injury and the maintenance of corticospinal topography.早期脊髓损伤后皮质脊髓轴突的延伸与再生以及皮质脊髓拓扑结构的维持
Exp Neurol. 1993 Sep;123(1):106-17. doi: 10.1006/exnr.1993.1144.
4
Spinal cord plasticity in response to unilateral inhibition of the rat motor cortex during development: changes to gene expression, muscle afferents and the ipsilateral corticospinal projection.发育过程中大鼠运动皮层单侧抑制后脊髓可塑性:基因表达、肌肉传入神经及同侧皮质脊髓投射的变化
Eur J Neurosci. 2004 Nov;20(10):2555-66. doi: 10.1111/j.1460-9568.2004.03713.x.
5
Bilateral corticospinal projections arise from each motor cortex in the macaque monkey: a quantitative study.猕猴双侧皮质脊髓投射起源于每个运动皮层:一项定量研究。
J Comp Neurol. 2004 May 24;473(2):147-61. doi: 10.1002/cne.20051.
6
Prolonged local neurotrophin-3 infusion reduces ipsilateral collateral sprouting of spared corticospinal axons in adult rats.长期局部注入神经营养因子-3可减少成年大鼠中未受损皮质脊髓轴突的同侧侧支发芽。
Neuroscience. 2005;130(4):875-87. doi: 10.1016/j.neuroscience.2004.10.018.
7
Postnatal development of the ipsilateral corticospinal component in rat spinal cord: a light and electron microscopic anterograde HRP study.大鼠脊髓同侧皮质脊髓成分的出生后发育:光镜和电镜下的顺行性HRP研究
J Comp Neurol. 1992 Dec 1;326(1):133-46. doi: 10.1002/cne.903260112.
8
Distribution of corticospinal motor neurons in the postnatal rat: quantitative evidence for massive collateral elimination and modest cell death.出生后大鼠皮质脊髓运动神经元的分布:大量侧支消除和适度细胞死亡的定量证据
J Comp Neurol. 1994 Sep 1;347(1):115-26. doi: 10.1002/cne.903470109.
9
Formation of descending pathways mediating cortical command to forelimb motoneurons in neonatally hemidecorticated rats.介导皮质命令至新生期半脑切除大鼠前肢运动神经元的下行通路的形成。
J Neurophysiol. 2010 Sep;104(3):1707-16. doi: 10.1152/jn.00968.2009. Epub 2010 Jul 21.
10
Long ascending propriospinal projections from lumbosacral to upper cervical spinal cord in the rat.大鼠中从腰骶部到颈髓上部的长距离上升性脊髓固有投射。
Brain Res. 2006 Nov 13;1119(1):76-85. doi: 10.1016/j.brainres.2006.08.063. Epub 2006 Sep 22.

引用本文的文献

1
Fast Blue and Cholera Toxin-B Survival Guide for Alpha-Motoneurons Labeling: Less Is Better in Young B6SJL Mice, but More Is Better in Aged C57Bl/J Mice.用于α运动神经元标记的快蓝和霍乱毒素B存活指南:在年轻的B6SJL小鼠中越少越好,但在老年C57Bl/J小鼠中越多越好。
Bioengineering (Basel). 2023 Jan 20;10(2):141. doi: 10.3390/bioengineering10020141.
2
Comprehensive analysis of neonatal versus adult unilateral decortication in a mouse model using behavioral, neuroanatomical, and DNA microarray approaches.使用行为学、神经解剖学和DNA微阵列方法对小鼠模型中的新生与成年单侧去皮质进行综合分析。
Int J Mol Sci. 2014 Dec 5;15(12):22492-517. doi: 10.3390/ijms151222492.
3
Special function of nestin(+) neurons in the medial septum-diagonal band of Broca in adult rats.
成年大鼠隔内侧核-布鲁卡斜角带巢蛋白(+)神经元的特殊功能。
Neural Regen Res. 2014 Feb 1;9(3):308-17. doi: 10.4103/1673-5374.128229.
4
Sprouting of brainstem-spinal tracts in response to unilateral motor cortex stroke in mice.小鼠单侧大脑皮层卒中后脑干-脊髓束的发芽。
J Neurosci. 2014 Feb 26;34(9):3378-89. doi: 10.1523/JNEUROSCI.4384-13.2014.