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Axonal degenerations with aging and their rescue by genetic and nutritional manipulations

Research Project

Project/Area Number 16590158
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field General anatomy (including Histology/Embryology)
Research InstitutionKoshien University

Principal Investigator

GOTOW Takahiro  Koshien University, College of Nutrition, Professor, 栄養学部, 教授 (20135693)

Co-Investigator(Kenkyū-buntansha) UCHIYAMA Yasuo  Osaka University Graduate School of Medicine, Department of Cell Biology and Neuroscience, Professor, 大学院・医学系研究科, 教授 (10049091)
Project Period (FY) 2004 – 2005
Project Status Completed (Fiscal Year 2005)
Budget Amount *help
¥3,200,000 (Direct Cost: ¥3,200,000)
Fiscal Year 2005: ¥1,300,000 (Direct Cost: ¥1,300,000)
Fiscal Year 2004: ¥1,900,000 (Direct Cost: ¥1,900,000)
Keywordssenescence-accelerated mice / stroke-prone spontaneous hypertensive rat / neuron / axon / polyphenol / cytoskeletons / lysosome / cell death-associated proteins / 肝細胞 / 赤ワイン / ウコン / 免疫組織細胞化学 / ウエスタンブロット
Research Abstract

We analyzed biochemically and morphologically neurons, especially their axons, in the central nervous system (CNS) of senescence-accelerated mice, SAMP10 and klotho mutant mice, and stroke-prone spontaneously hypertensive rats (SHRSP), and found that these axons showed degenerative profiles expanded with accumulation of cell organells such as neurofilaments (NFs), lysosomes and mitochondria. Since the polyphenol of red wine is considered to be effective to prevent arteriosclerosis-associated diseases, we administrated the red wine in comparison with other alcohols, Japanese sake and diluted ethanol (concentration of ethanol was the same, 14%, in all cases). Compared to the control (water dosage), the cellular damages, such as increases of NFs and lipofuscin granules, which were similar to those seen in aged animals, were observed, but the mildest in the alteration with the red wine. Turmeric also showed inhibition of the appearance of cellular damages by alcohols. Therefore, both polyphonols appear to be effective for preventing or delaying cellular damages caused by aging or age-related disorders. We are going to analyze whether pholyphenols alone have such powerful effects to extend the lifespan of these animals. The klotho mutant mice were not sure whether they showed senescence-associated disorders because of their too short lifespan (2 months), but the overexpression of klotho gene showed significant extended longevity. We also concentrated on analyzing alterations in nature of CNS neurons and glial cells of these mice, and found that in them biochemically the proteins expressed in these cells, which increase in aged animals, increased in expression, while those decreasing with aging were reduced, and morphologically, NFs and lysosomes increased significantly, while synapse-associated profiles decreased. The results indicate that klotho mutant mice are useful as well as convenient animal model for the human aging.

Report

(3 results)
  • 2005 Annual Research Report   Final Research Report Summary
  • 2004 Annual Research Report
  • Research Products

    (6 results)

All 2006 2005

All Journal Article (6 results)

  • [Journal Article] Aggregate formation and phosphorylation of neurofilament-L Pro22 Charcot-Marie-Tooth disease mutants2006

    • Author(s)
      Sasaki, T. et al.
    • Journal Title

      Human Molecular Genetics 15(6)

      Pages: 943-952

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2005 Final Research Report Summary
  • [Journal Article] Participation of autophagy in strage of lysosomes in neurons from mouse models of neuronal ceroid-lipofuscinoses(Batten Disease)2005

    • Author(s)
      Koike, M.
    • Journal Title

      American Journal of Pathology 167・6

      Pages: 1713-1728

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2005 Final Research Report Summary
  • [Journal Article] Aggregate formation and phosphorylation of neurofilament-L Pro22 Charcot-Marie-Tooth discase mutants2005

    • Author(s)
      Sasaki, T.
    • Journal Title

      Human Molecular Genetics 15・6

      Pages: 943-952

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2005 Final Research Report Summary
  • [Journal Article] Participation of autophagy in storage of lysosomes in neurons from mouse models of neuronal ceroid-lipofuscinoses (Batten Disease)2005

    • Author(s)
      Koike, M. et al.
    • Journal Title

      American Journal of Pathology 167(6)

      Pages: 1713-1728

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2005 Final Research Report Summary
  • [Journal Article] Participation of autophagy in storage of lysosomes in neurons from mouse models of neuronal ceroid-lipofuscinoses (Batten Disease)2005

    • Author(s)
      Koike, M.
    • Journal Title

      American Journal of Pathology 167・6

      Pages: 1713-1728

    • Related Report
      2005 Annual Research Report
  • [Journal Article] Aggregate formation and phosphorylation of neurofilament-L Pro22 Charcot-Marie-Tooth disease mutants2005

    • Author(s)
      Sasaki, T.
    • Journal Title

      Human Molecular Genetics 15・6

      Pages: 943-952

    • Related Report
      2005 Annual Research Report

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Published: 2004-04-01   Modified: 2016-04-21  

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