Studies on the Mechanism of Cell Deterioration for the Prevention of Aging through Dietary Life

通过饮食生活预防衰老的细胞退化机制研究

基本信息

项目摘要

Lipid peroxidation traditionally has been regarded as the major process causing damage to the brain by oxygen radicals and, subsequently, some forms of age-related deterioration. The brain, with its high oxygen consumption and abundance of polyunsaturated fatty acids, is at risk for oxidative damage. Although a great number of reports have associated lipid peroxidation with neurodegenerative diseases, the precise target of lipid peroxidation remains unclear. The aim of this study was to clarify the precise target of lipid hydroperoxides in neuronal cells. In this study, we showed the deleterious effect of phosphatidylcholine hydroperoxides (PCOOH) on PC 12 cells before and after differentiation into neuronal cells. Cell viability was significantly decreased in differentiated cells treated with PCOOH compared to undifferentiated cells treated in a similar way. PCOOH disrupted the formation of neurites and neuronal microtubules, which consist mainly of tubulin. Our results showed that differentiated cells were more vulnerable than undifferentiated cells to PCOOH and that PCOOH could attack microtubule-tubulin systems. This is the first study to clarify the effect on neuronal cells of PCOOH produced in the early stage of neurodegenerative disease and to elucidate the target of lipid hydroperoxide.
脂质过氧化传统上被认为是氧自由基对大脑造成损伤的主要过程,并随后导致某些形式的与年龄相关的退化。大脑因其高耗氧量和丰富的多不饱和脂肪酸,有氧化损伤的风险。尽管大量的报道将脂质过氧化与神经退行性疾病联系起来,但脂质过氧化的确切目标仍不清楚。本研究的目的是阐明脂质氢过氧化物在神经元细胞中的精确靶点。在本研究中,我们展示了磷脂酰胆碱氢过氧化物(PCOOH)对pc12细胞分化为神经元细胞前后的有害作用。与未分化细胞相比,经PCOOH处理的分化细胞的细胞活力显著降低。PCOOH破坏主要由微管蛋白组成的神经突和神经元微管的形成。我们的研究结果表明,分化的细胞比未分化的细胞更容易受到PCOOH的攻击,PCOOH可以攻击微管-微管蛋白系统。本研究首次阐明了神经退行性疾病早期产生的PCOOH对神经元细胞的影响,并阐明了脂质过氧化氢的作用靶点。

项目成果

期刊论文数量(14)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
日本産大麦分級粉からの微小管形成促進物質の精製
日本大麦粉中微管形成促进物质的纯化
  • DOI:
  • 发表时间:
    2007
  • 期刊:
  • 影响因子:
    0
  • 作者:
    川口真規子;関口綾子;山中裕佳子;土井裕司
  • 通讯作者:
    土井裕司
Sustrate specificity of aminopeptidase from Japanese classified barley flour
日本分级大麦粉氨肽酶的底物特异性
Effects on immune response of antidiabetic ingredients from white-skinned sweet potato (Jpomoea batatas L.)
白皮甘薯 (Jpomoea batatas L.) 抗糖尿病成分对免疫反应的影响
  • DOI:
  • 发表时间:
    2005
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Miyazaki;Yoshiko;Kusano;Shuichi;Doi;Hiroshi;Aki;Osami
  • 通讯作者:
    Osami
Purification of microtubule assembly promoting material from Japanese classified barley flour
日本分级大麦粉中微管组装促进物质的纯化
  • DOI:
  • 发表时间:
    2007
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Kawaguchi;Makiko;Sekiguchi;Ayako;Yamanaka;Yukako;Doi;Hiroshi
  • 通讯作者:
    Hiroshi
Sustrate specificity of aminopeptidase from Japanese classified barley flour.
日本分级大麦粉氨肽酶的基质特异性。
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DOI Hiroshi其他文献

DOI Hiroshi的其他文献

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{{ truncateString('DOI Hiroshi', 18)}}的其他基金

Elucidation of pathophysiology and development of treatment for spinocerebellar ataxia using a novel mouse model
使用新型小鼠模型阐明脊髓小脑共济失调的病理生理学和治疗方法的开发
  • 批准号:
    18K07503
  • 财政年份:
    2018
  • 资助金额:
    $ 2.37万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Research on Secret Sharing Scheme Considering Lifecycle of Information
考虑信息生命周期的秘密共享方案研究
  • 批准号:
    18K11306
  • 财政年份:
    2018
  • 资助金额:
    $ 2.37万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Assessment of an experimental re-irradiation model
实验再辐照模型的评估
  • 批准号:
    17K16493
  • 财政年份:
    2017
  • 资助金额:
    $ 2.37万
  • 项目类别:
    Grant-in-Aid for Young Scientists (B)
Analysis of genetic back ground and pathomechanism of spinocerebellar degeneration
脊髓小脑变性的遗传背景及发病机制分析
  • 批准号:
    15K09344
  • 财政年份:
    2015
  • 资助金额:
    $ 2.37万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Research for the extensions of searchable encryption schemes
可搜索加密方案的扩展研究
  • 批准号:
    25330161
  • 财政年份:
    2013
  • 资助金额:
    $ 2.37万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Exome analysis of spinocerebellar ataxias
脊髓小脑共济失调的外显子组分析
  • 批准号:
    24790893
  • 财政年份:
    2012
  • 资助金额:
    $ 2.37万
  • 项目类别:
    Grant-in-Aid for Young Scientists (B)
Detection of Nobel Food Components for Preventing Altheimer's Disease and Evidence of its Action Mechanizum
检测用于预防阿尔海默病的诺贝尔食品成分及其作用机制的证据
  • 批准号:
    23500985
  • 财政年份:
    2011
  • 资助金额:
    $ 2.37万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Isolation of causative genes for recessive spinocerebellar ataxia
隐性脊髓小脑共济失调致病基因的分离
  • 批准号:
    22790823
  • 财政年份:
    2010
  • 资助金额:
    $ 2.37万
  • 项目类别:
    Grant-in-Aid for Young Scientists (B)
Development of foodstuffs for the prevention of ageing based on the cell deterioration mechanism
基于细胞劣化机制开发预防衰老食品
  • 批准号:
    20500731
  • 财政年份:
    2008
  • 资助金额:
    $ 2.37万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
A Study of Vaccine Therapy for Prostate Cancer Using Prostate Stem Cell Antigen (PSCA)-Transfected Dendritic Cells
使用前列腺干细胞抗原(PSCA)转染的树突状细胞进行前列腺癌疫苗治疗的研究
  • 批准号:
    14571527
  • 财政年份:
    2002
  • 资助金额:
    $ 2.37万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)

相似海外基金

Clinical roles of plasma phosphatidylcholine hydroperoxide-reducing activity in the development of pre-eclampsia
血浆磷脂酰胆碱过氧化氢还原活性在先兆子痫发生中的临床作用
  • 批准号:
    09671716
  • 财政年份:
    1997
  • 资助金额:
    $ 2.37万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Pathogenesis of hepatic injury in endotoxemia: with special reference to phosphatidylcholine hydroperoxide accumulation
内毒素血症肝损伤的发病机制:特别涉及氢过氧化磷脂酰胆碱的积累
  • 批准号:
    03454312
  • 财政年份:
    1991
  • 资助金额:
    $ 2.37万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (B)
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