• 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

Plasticity of the synaptic contact zone following loss of synapses in the cerebral cortex of aging humans.

作者信息

Adams I

机构信息

Department of Anatomy and Human Biology, University of Western Australia, Nedlands.

出版信息

Brain Res. 1987 Oct 27;424(2):343-51. doi: 10.1016/0006-8993(87)91479-x.

DOI:10.1016/0006-8993(87)91479-x
PMID:3676832
Abstract

Quantitative ultrastructural analyses of ethanolic phosphotungstic acid-stained human layer 1 precentral motor cortex (Brodmann's area 4) and layer 1 postcentral somatosensory cortex (Brodmann's area 3) were undertaken to determine the nature of synaptic changes occurring over a series of ages (45-84 years) of a normal aging human population. In the precentral cortex, a significant decrease in the number of synapses was accompanied by an increase in mean length of the postsynaptic contact zone and a decrease in the mean width of the presynaptic paramembranous density. The frequency of mature type A and immature type E synaptic profiles decreased with age. There were no changes in the width of the postsynaptic paramembranous density, cleft width or the number of presynaptic dense projections per synapse. In the postcentral cortex there were no significant changes in synaptic number or in any of the synaptic parameters measured. The present study demonstrates that age-related synapse loss in the human cerebral cortex may be confined to specific cortical regions. The data suggest that in the precentral cortex the plasticity of the synaptic contact zone may be a compensatory response by the remaining synapses to age-related synapse loss.

摘要

相似文献

1
Plasticity of the synaptic contact zone following loss of synapses in the cerebral cortex of aging humans.
Brain Res. 1987 Oct 27;424(2):343-51. doi: 10.1016/0006-8993(87)91479-x.
2
Comparison of synaptic changes in the precentral and postcentral cerebral cortex of aging humans: a quantitative ultrastructural study.
Neurobiol Aging. 1987 May-Jun;8(3):203-12. doi: 10.1016/0197-4580(87)90003-0.
3
Synaptic density in human frontal cortex - developmental changes and effects of aging.人类额叶皮质中的突触密度——发育变化及衰老的影响
Brain Res. 1979 Mar 16;163(2):195-205. doi: 10.1016/0006-8993(79)90349-4.
4
Structural plasticity of synapses in Alzheimer's disease.阿尔茨海默病中突触的结构可塑性
Mol Neurobiol. 1991;5(2-4):411-9. doi: 10.1007/BF02935562.
5
Synaptic structural changes during development and aging.
Brain Res. 1987 Oct;432(2):239-48. doi: 10.1016/0165-3806(87)90048-4.
6
[Ultrastructural variations of synapses in the normal human cerebral cortex].[正常人大脑皮质突触的超微结构变异]
Bull Assoc Anat (Nancy). 1976 Mar;60(168):231-41.
7
Quantitative assessment of cortical synaptic density in Alzheimer's disease.阿尔茨海默病中皮质突触密度的定量评估。
Neurobiol Aging. 1990 Jan-Feb;11(1):29-37. doi: 10.1016/0197-4580(90)90059-9.
8
Changes in the length and width of the postsynaptic density, the width of the intersynaptic density and the synaptic cleft in the cerebral cortex synapses of rats exposed to prolonged aerogenic hypoxia during early ontogenesis. An electron microscopic morphometric study.早期个体发育期间暴露于长时间气体性缺氧的大鼠大脑皮质突触中突触后致密物的长度和宽度、突触间致密物的宽度以及突触间隙的变化。一项电子显微镜形态计量学研究。
Physiol Bohemoslov. 1980;29(6):561-7.
9
Perforated and non-perforated synapses in rat neocortex: three-dimensional reconstructions.大鼠新皮质中的穿孔和非穿孔突触:三维重建
Brain Res. 1991 Aug 16;556(2):247-58. doi: 10.1016/0006-8993(91)90312-j.
10
[Ultrastructure of human cerebral cortical synapses: age-specific aspects].[人类大脑皮质突触的超微结构:年龄特异性方面]
Vestn Ross Akad Med Nauk. 2002(6):27-31.

引用本文的文献

1
Alzheimer's disease as a synaptopathy: Evidence for dysfunction of synapses during disease progression.阿尔茨海默病作为一种突触病:疾病进展过程中突触功能障碍的证据。
Front Synaptic Neurosci. 2023 Mar 9;15:1129036. doi: 10.3389/fnsyn.2023.1129036. eCollection 2023.
2
Three-dimensional analysis of synaptic organization in the hippocampal CA1 field in Alzheimer's disease.阿尔茨海默病中海马 CA1 区突触组织的三维分析。
Brain. 2021 Mar 3;144(2):553-573. doi: 10.1093/brain/awaa406.
3
Receptor Tyrosine Kinases as Therapeutic Targets for Alcohol Use Disorder.
受体酪氨酸激酶作为治疗酒精使用障碍的靶点。
Neurotherapeutics. 2020 Jan;17(1):4-16. doi: 10.1007/s13311-019-00795-4.
4
Transmission Electron Microscopy Study of Mitochondria in Aging Brain Synapses.衰老脑突触中线粒体的透射电子显微镜研究
Antioxidants (Basel). 2019 Jun 11;8(6):171. doi: 10.3390/antiox8060171.
5
Differential effects of motor cortical excitability and plasticity in young and old individuals: a Transcranial Magnetic Stimulation (TMS) study.年轻人和老年人运动皮层兴奋性及可塑性的差异效应:一项经颅磁刺激(TMS)研究
Front Aging Neurosci. 2014 Jun 10;6:111. doi: 10.3389/fnagi.2014.00111. eCollection 2014.
6
Interindividual variability and age-dependency of motor cortical plasticity induced by paired associative stimulation.配对联想刺激诱导的运动皮质可塑性的个体间变异性和年龄依赖性。
Exp Brain Res. 2008 May;187(3):467-75. doi: 10.1007/s00221-008-1319-7. Epub 2008 Mar 5.
7
The optimal height of the synaptic cleft.突触间隙的最佳高度。
Proc Natl Acad Sci U S A. 2007 Feb 6;104(6):1823-8. doi: 10.1073/pnas.0606636104. Epub 2007 Jan 29.
8
Age and sex differences in human motor cortex input-output characteristics.人类运动皮层输入-输出特征的年龄和性别差异。
J Physiol. 2003 Jan 15;546(Pt 2):605-13. doi: 10.1113/jphysiol.2002.029454.
9
Synaptic pathology and glial responses to neuronal injury precede the formation of senile plaques and amyloid deposits in the aging cerebral cortex.在衰老的大脑皮质中,突触病理学以及胶质细胞对神经元损伤的反应先于老年斑和淀粉样沉积物的形成。
Am J Pathol. 1994 Dec;145(6):1358-81.
10
Structural plasticity of synapses in Alzheimer's disease.阿尔茨海默病中突触的结构可塑性
Mol Neurobiol. 1991;5(2-4):411-9. doi: 10.1007/BF02935562.