• 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

“红皇后假说”框架下的神经元可塑性与衰老过程

Neuronal plasticity and ageing processes in the frame of the 'Red Queen Theory'.

作者信息

Agnati L F, Zoli M, Biagini G, Fuxe K

机构信息

Institute of Human Physiology, University of Modena, Italy.

出版信息

Acta Physiol Scand. 1992 Aug;145(4):301-9. doi: 10.1111/j.1748-1716.1992.tb09370.x.

DOI:10.1111/j.1748-1716.1992.tb09370.x
PMID:1529720
Abstract

On the basis of the morphofunctional evidence obtained in old brains of humans and mammals the present hypothesis has been introduced. This hypothesis states that neuronal plasticity can be used either to compensate for neuronal degeneration or to store new information. Thus, in pathological ageing the marked rate of degeneration has fully exhausted the already reduced plasticity capability of neural networks. In this way marked impairments of memory trace formation take place in pathological ageing conditions such as Alzheimer's disease. The essence of this hypothesis is that a competition for the available plasticity exists between the compensatory responses to ageing-induced degeneration and the processes necessary for memory trace formation. We have called this hypothesis the 'Red Queen Theory', an analogy borrowed from Lewis Carroll's book Through the Looking Glass. Thus, in ageing, processes responsible for plasticity must be forced to run at the highest possible rate to maintain the morphofunctional substrate of the existing networks as well as to allow the formation of new memory traces.

摘要

基于在人类和哺乳动物老年大脑中获得的形态功能证据,提出了本假说。该假说指出,神经元可塑性可用于补偿神经元退化或存储新信息。因此,在病理性衰老中,显著的退化率已完全耗尽了神经网络已经降低的可塑性能力。这样,在诸如阿尔茨海默病等病理性衰老条件下,记忆痕迹形成会出现明显受损。该假说的核心是,在对衰老诱导的退化的代偿反应与记忆痕迹形成所需的过程之间,存在对可用可塑性的竞争。我们将此假说称为“红皇后理论”,这是从刘易斯·卡罗尔的《镜中世界》一书中借用的类比。因此,在衰老过程中,负责可塑性的过程必须被迫以尽可能高的速率运行,以维持现有网络的形态功能基础,并允许形成新的记忆痕迹。

相似文献

1
Neuronal plasticity and ageing processes in the frame of the 'Red Queen Theory'.“红皇后假说”框架下的神经元可塑性与衰老过程
Acta Physiol Scand. 1992 Aug;145(4):301-9. doi: 10.1111/j.1748-1716.1992.tb09370.x.
2
Cerebral restorative plasticity from normal ageing to brain diseases: a "never ending story".正常衰老到脑部疾病的大脑修复性可塑性:一个“永无止境的故事”。
Restor Neurol Neurosci. 2010;28(3):349-66. doi: 10.3233/RNN-2010-0538.
3
Neural plasticity in the ageing brain.衰老大脑中的神经可塑性。
Nat Rev Neurosci. 2006 Jan;7(1):30-40. doi: 10.1038/nrn1809.
4
Molecular mechanisms mediating pathological plasticity in Huntington's disease and Alzheimer's disease.介导亨廷顿舞蹈症和阿尔茨海默病病理可塑性的分子机制。
J Neurochem. 2007 Feb;100(4):874-82. doi: 10.1111/j.1471-4159.2006.04275.x. Epub 2007 Jan 8.
5
Dendritic reorganisation in the basal forebrain under degenerative conditions and its defects in Alzheimer's disease. II. Ageing, Korsakoff's disease, Parkinson's disease, and Alzheimer's disease.退行性病变条件下基底前脑的树突重组及其在阿尔茨海默病中的缺陷。II. 衰老、科萨科夫综合征、帕金森病和阿尔茨海默病
J Comp Neurol. 1995 Jan 9;351(2):189-222. doi: 10.1002/cne.903510203.
6
SCG10-related neuronal growth-associated proteins in neural development, plasticity, degeneration, and aging.与SCG10相关的神经元生长相关蛋白在神经发育、可塑性、退化和衰老中的作用。
J Neurosci Res. 2002 Nov 1;70(3):264-73. doi: 10.1002/jnr.10353.
7
New life in an old idea: the synaptic plasticity and memory hypothesis revisited.旧观念中的新生命:重新审视突触可塑性与记忆假说
Hippocampus. 2002;12(5):609-36. doi: 10.1002/hipo.10107.
8
Toward understanding of the molecular basis of loss of neuronal plasticity in ageing.迈向对衰老过程中神经元可塑性丧失的分子基础的理解。
Age Ageing. 1993 Jan;22(1):S5-18.
9
Decrease in highly polysialylated neuronal cell adhesion molecules and in spatial learning during ageing are not correlated.衰老过程中高度多聚唾液酸化的神经元细胞黏附分子减少与空间学习能力下降并无关联。
Brain Res. 1997 Jan 9;744(2):285-92. doi: 10.1016/S0006-8993(96)01115-8.
10
Correlation of cellular changes and spatial memory during aging in rats.大鼠衰老过程中细胞变化与空间记忆的相关性
Exp Gerontol. 2008 Oct;43(10):929-38. doi: 10.1016/j.exger.2008.08.002. Epub 2008 Aug 12.

引用本文的文献

1
Peptide-Drug Conjugates: An Emerging Direction for the Next Generation of Peptide Therapeutics.肽药物偶联物:下一代肽治疗药物的新兴方向。
J Med Chem. 2024 Feb 8;67(3):1641-1661. doi: 10.1021/acs.jmedchem.3c01835. Epub 2024 Jan 26.
2
Novel Enzyme Replacement Therapies for Neuropathic Mucopolysaccharidoses.新型酶替代疗法治疗神经病变黏多糖贮积症。
Int J Mol Sci. 2020 Jan 8;21(2):400. doi: 10.3390/ijms21020400.
3
Old Drugs as New Treatments for Neurodegenerative Diseases.老药作为神经退行性疾病的新疗法
Pharmaceuticals (Basel). 2018 May 11;11(2):44. doi: 10.3390/ph11020044.
4
Interactions Between Epilepsy and Plasticity.癫痫与可塑性之间的相互作用
Pharmaceuticals (Basel). 2018 Feb 7;11(1):17. doi: 10.3390/ph11010017.
5
A window into the heterogeneity of human cerebrospinal fluid Aβ peptides.洞察人类脑脊液Aβ肽的异质性
J Biomed Biotechnol. 2011;2011:697036. doi: 10.1155/2011/697036. Epub 2011 Aug 23.
6
Common key-signals in learning and neurodegeneration: focus on excito-amino acids, beta-amyloid peptides and alpha-synuclein.学习与神经退行性变中的常见关键信号:聚焦于兴奋性氨基酸、β-淀粉样肽和α-突触核蛋白。
J Neural Transm (Vienna). 2009 Aug;116(8):953-74. doi: 10.1007/s00702-008-0150-4. Epub 2008 Nov 19.
7
Age-related structural and functional characteristics of rabbit hippocampal neurons during the formation of temporal associations.
Neurosci Behav Physiol. 2004 Nov;34(9):889-96. doi: 10.1023/b:neab.0000042573.05342.95.
8
Spatial memory performances of aged rats in the water maze predict levels of hippocampal neurogenesis.老年大鼠在水迷宫中的空间记忆表现可预测海马神经发生水平。
Proc Natl Acad Sci U S A. 2003 Nov 25;100(24):14385-90. doi: 10.1073/pnas.2334169100. Epub 2003 Nov 12.