Models of catastrophic cortical plasticity contributing
灾难性皮质可塑性贡献模型
基本信息
- 批准号:6663430
- 负责人:
- 金额:$ 20.73万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2002
- 资助国家:美国
- 起止时间:2002-05-01 至 2003-04-30
- 项目状态:已结题
- 来源:
- 关键词:Aotus auditory cortex behavior test behavioral /social science research tag brain mapping developmental disease /disorder disease /disorder model dystonia electrophysiology experience laboratory rat learning method development motor cortex nervous system disorder neural information processing neural plasticity neuromuscular disorder neurons neuropathology neuropsychology psychomotor function sensorimotor system sensory cortex sensory feedback somesthetic sensory cortex speech
项目摘要
The overall objective of this project is to determine specific ways in which learning-induced changes in cortical representations contribute to the origins of and the expressions of acquired and developmental movement disorders and severe disorders of language, and to use that understanding as a source of insight for defining the forms of new neuroscience-based therapies designed to remediate them. We shall further develop and elaborate models of origin of a) focal dystonias of the hand (fDh); b) the usually-severe language disorder component of pervasive developmental disorders (PDDs); and c) some forms of generalized developmental dystonia and cerebral generate representations of learned stimuli and behaviors. It has already contributed to a growing appreciation of what postnatal functional self-organizing mechanisms contribute to human performance ability and disability and to the specific mechanisms that underlie these cortical cellular, synaptic and circuit changes process. Our principal focus is directed toward creating special models of "catastrophic plasticity" that have human neuropathology parallels. It is hypothesized that catastrophic cortical plasticity underlies the emergence of acquired movement disorders and repetitive strain injury symptoms in adults, and accounts for some of the major deficits of pervasive developmental disorders, developmental generalized dystonias and some forms of cerebral palsy. A more complete understanding of the neurological origins of the deficits contributed by the progressive learning in a defectively functionally self- organizing brains will provide crucial insights into possible forms of a new class of remediative training strategies and our understanding the physiological impacts of brain trauma, oxygen deprivation, or inherited weaknesses that contribute-along with learning to the origins of these severely disabling conditions. The continuation experiments are designed to deepen our understanding of the complex neurological origins of these common human maladies, and to provide us with information that will guide the development of remedial training strategies that could allow us to more effectively help many of these severely impaired individuals.
该项目的总体目标是确定学习引起的皮质表征变化对获得性和发育性运动障碍以及严重语言障碍的起源和表达的具体方式,并将这种理解作为定义旨在补救它们的新的基于神经科学的疗法形式的洞察力来源。我们将进一步发展和阐述以下起源的模型:a)手部局灶性肌张力障碍(fDh); B)广泛性发育障碍(PDDs)中通常严重的语言障碍成分;以及c)某些形式的全身性发育性肌张力障碍和大脑对学习刺激和行为的生成表征。它已经促进了人们对产后功能性自组织机制对人类表现能力和残疾的贡献以及这些皮层细胞,突触和电路变化过程的具体机制的日益认识。我们的主要重点是创造具有人类神经病理学相似性的“灾难性可塑性”的特殊模型。 据推测,灾难性的皮质可塑性的基础上出现的获得性运动障碍和重复性劳损损伤症状的成年人,并占一些主要缺陷的广泛性发育障碍,发育性全身性肌张力障碍和某些形式的脑瘫。在一个有缺陷的功能自组织大脑中,对由渐进学习所造成的缺陷的神经学起源的更全面的理解,将为我们提供关键的见解,以了解一类新的补救训练策略的可能形式,以及我们对脑创伤、缺氧或遗传性弱点的生理影响,这些生理影响与学习一起促成了这些严重残疾状况的起源。延续实验旨在加深我们对这些常见人类疾病的复杂神经起源的理解,并为我们提供指导补救训练策略的发展的信息,使我们能够更有效地帮助许多这些严重受损的个体。
项目成果
期刊论文数量(0)
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MICHAEL M MERZENICH其他文献
MICHAEL M MERZENICH的其他文献
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{{ truncateString('MICHAEL M MERZENICH', 18)}}的其他基金
Models of catastrophic cortical plasticity contributing
灾难性皮质可塑性贡献模型
- 批准号:
6588521 - 财政年份:2002
- 资助金额:
$ 20.73万 - 项目类别:
CORTICAL PLASTICITY--LEARNING ORIGINS OF HUMAN DISABILITY
皮质可塑性--学习人类残疾的起源
- 批准号:
6449802 - 财政年份:2001
- 资助金额:
$ 20.73万 - 项目类别:
CORTICAL PLASTICITY--LEARNING ORIGINS OF HUMAN DISABILITY
皮质可塑性--学习人类残疾的起源
- 批准号:
6323425 - 财政年份:2000
- 资助金额:
$ 20.73万 - 项目类别:
CORTICAL PLASTICITY--LEARNING ORIGINS OF HUMAN DISABILITY
皮质可塑性--学习人类残疾的起源
- 批准号:
6314151 - 财政年份:2000
- 资助金额:
$ 20.73万 - 项目类别:
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