The study of pathophysiological mechanism for the subcortical dementia- an evaluation using event-related potentials tomography

皮层下痴呆病理生理机制研究——事件相关电位断层扫描评估

基本信息

  • 批准号:
    11670637
  • 负责人:
  • 金额:
    $ 0.9万
  • 依托单位:
  • 依托单位国家:
    日本
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
  • 财政年份:
    1999
  • 资助国家:
    日本
  • 起止时间:
    1999 至 2000
  • 项目状态:
    已结题

项目摘要

To evaluate the pathophysiological changes in subcortical dementia, electrical filed of the event-related potentials were analyzed. As the fundamental study, we examined the effect of task relevance and the novelty of P3a components in an auditory study. Our data suggest that the characterization of novelty P300 may depend on the mental resources that can be devoted to novel stimuli during parallel processing.After the fundamental study, we evaluated the characteristics of information processing disturbance in patients with vascular dementia (VaD) using auditory oddball and 4-tone paradigms. The data suggest that the characteristics of mental dysfunction in mild VaD patients do not only depend on abnormal information processing speed but also abnormal mental resource allocation.The 3rd study is the evaluation of pathophysiological mechanism for the Parkinson's disease as subcortical dementia. Event-related potentials topography produced by novel and target stimuli was used to detect dysfunction of mental switching (perseveration) in Parkinson's disease Parkinson's disease patients (PDPs). Our findings suggest that decreased mental switching causes lack of novelty P3 habituation in PDPs and that this is related to learning disability based on dysfunction of frontal lobe and basal ganglia.Finally, we investigated whether early information processing for auditory sensory input would be hindered in PDPs. The data indicated that there are dysfunction both of automatic and controlled processing in the information processing for auditory sensory input in the PDP.
为探讨皮层下痴呆的病理生理改变,对皮层下痴呆的事件相关电位进行了分析。作为基础研究,我们考察了任务相关性和听觉P3a成分的新奇的影响。我们的研究结果表明,新奇P300的表征可能依赖于平行加工过程中用于新颖刺激的心理资源。在基础研究之后,我们采用听觉oddball范式和4音范式评价了血管性痴呆(VaD)患者的信息加工障碍特征。提示轻度VaD患者的心理功能障碍不仅表现为信息加工速度的异常,还表现为心理资源分配的异常。第三部分是帕金森病皮层下痴呆的病理生理机制的评价。采用事件相关电位地形图检测帕金森病患者的心理转换功能障碍。我们的研究结果表明,减少心理转换的原因缺乏新奇的P3习惯化的PDP,这是与学习障碍的基础上的额叶和基底ganglia.Finally,我们调查是否会阻碍早期信息加工的听觉感觉输入的PDP。实验结果表明,PDP对听觉感觉输入的信息加工存在自动加工和控制加工功能障碍。

项目成果

期刊论文数量(22)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Akinori Hozumi, Koichi Hirata, et al: "An application of four-tone paradigm for the evaluation of cognitive function in vascular dementia."J J Clin.Neurophysiol. 28 (In Japanese). 46-50 (2000)
Akinori Hozumi、Koichi Hirata 等人:“四音范式在评估血管性痴呆认知功能中的应用。”J J Clin.Neurophysiol。
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  • 影响因子:
    0
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A.Hozumi, et.al.: "Perseveration for Novel Stimuli in Parkinson's Disease : An Evaluation Based on Event-Related Potentials Topography."Movement Disorders. 15. 835-842 (2000)
A.Hozumi 等人:“帕金森病中新刺激的持久性:基于事件相关电位地形图的评估。”运动障碍。
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
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  • 通讯作者:
Kouichi Hirata(他2名,1番目): "A study of task irrevant and novelty for the P3a component"Electroencephalogr.Clin.Neurophysiol. 49(Suppl). 154-159 (1999)
Kouichi Hirata(其他 2 名,第 1 名):“P3a 成分的任务无关性和新颖性的研究”Electroencephalogr.Clin.Neurophysiol 49(增刊)。
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
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穂積昭則 他: "パーキンソン病患者の新奇刺激ERP"臨床脳波. 41. 207-211 (1999)
Akinori Hozumi 等人:“帕金森病患者的新型刺激 ERP”临床脑电图 41. 207-211 (1999)
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    0
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HIRATA Koichi其他文献

Effect of Fuel Component on Nitrous Oxide Emission Characteristics of Diesel Engine
燃料成分对柴油机氧化亚氮排放特性的影响
  • DOI:
  • 发表时间:
    2014
  • 期刊:
  • 影响因子:
    0
  • 作者:
    YOO Dong-Hoon;NISHIO Sumito;HIRATA Koichi
  • 通讯作者:
    HIRATA Koichi

HIRATA Koichi的其他文献

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{{ truncateString('HIRATA Koichi', 18)}}的其他基金

Fundamental Researches for the Application of Human Small Hepatocytes in Clinical Treatment
人小肝细胞在临床治疗中应用的基础研究
  • 批准号:
    25293289
  • 财政年份:
    2013
  • 资助金额:
    $ 0.9万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Developing a novel vaccine therapy targeting cancer stem cells
开发针对癌症干细胞的新型疫苗疗法
  • 批准号:
    24659592
  • 财政年份:
    2012
  • 资助金额:
    $ 0.9万
  • 项目类别:
    Grant-in-Aid for Challenging Exploratory Research
Clinical and Basic Researches of Hepatic Stem Cells onLiver Regeneration as Defense Mechanism.
肝干细胞作为肝脏再生防御机制的临床和基础研究。
  • 批准号:
    22390259
  • 财政年份:
    2010
  • 资助金额:
    $ 0.9万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Research of Origami Constructions as Geometric Teaching Materials
折纸结构作为几何教材的研究
  • 批准号:
    20500757
  • 财政年份:
    2008
  • 资助金额:
    $ 0.9万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Basic research objected to establish the highly qualified assessment of hepatic reserve function by utilizing new molecular marker localized in liver
基础研究旨在利用肝脏定位的新分子标记物建立高质量的肝储备功能评估
  • 批准号:
    19390353
  • 财政年份:
    2007
  • 资助金额:
    $ 0.9万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Research of the mechanism of non-obstructive cholestasis in severe infection and of the treatment for hepatic insufficiency
重症感染非梗阻性胆汁淤积机制及肝功能不全治疗的研究
  • 批准号:
    15390403
  • 财政年份:
    2003
  • 资助金额:
    $ 0.9万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
An evaluation of cognitive impairment related to cerebellar degeneration ; A study using event-related potentials
与小脑变性相关的认知障碍的评估;
  • 批准号:
    13670664
  • 财政年份:
    2001
  • 资助金额:
    $ 0.9万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Basic research of the treatment for hepatic failure by hepatocyte transplantation
肝细胞移植治疗肝衰竭的基础研究
  • 批准号:
    13557107
  • 财政年份:
    2001
  • 资助金额:
    $ 0.9万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Study of analysis of bile stasis using the extracorporeal hepatic tissue model and of the effect of cell transplantation on hepatic failure
体外肝组织模型分析胆汁瘀滞及细胞移植对肝衰竭影响的研究
  • 批准号:
    12470265
  • 财政年份:
    2000
  • 资助金额:
    $ 0.9万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Changes of bile canalicular contraction and of specific receptors on hepatocyte membrane during cholestasis in peri-operation.
围手术期胆汁淤积期间胆小管收缩及肝细胞膜特异性受体的变化
  • 批准号:
    09470256
  • 财政年份:
    1997
  • 资助金额:
    $ 0.9万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
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