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Studies on the inhibitory effect of vitamin E against secondary reaction of lipid peroxidation

Research Project

Project/Area Number 18580115
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Food science
Research InstitutionGifu University

Principal Investigator

YAMAUCHI Ryo  Gifu University, Faculty of Applied Biological Sciences, Professor (50126760)

Project Period (FY) 2006 – 2007
Project Status Completed (Fiscal Year 2007)
Budget Amount *help
¥3,870,000 (Direct Cost: ¥3,600,000、Indirect Cost: ¥270,000)
Fiscal Year 2007: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2006: ¥2,700,000 (Direct Cost: ¥2,700,000)
Keywordsvitamin E / lipid peroxidation / γ-tocopherol / 4-oxo-2-nonenal / 4-hvoiroxv-2-nonenal / 4-オキソ-2-ノネナール
Research Abstract

Oxidative cleavage of unsaturated lipids during peroxidation gives rise to cytotoxic and genotoxic a,β-unsaturated aldehydes, such as 4-hydroxy-2-nonenal (HNE) and 4-oxo-2-nonenal (ONE). We have studied the reactivity of vitamin E with HNE or ONE to clarify the role of vitamin E on the detoxification of α,β-unsaturated aldehydes. Α-Tocopherol (α-TH), the most active vitamin E, did not react with these aldehydes, whereas y- and δ- THs could react with ONE or HNE under the acidic conditions. ONE is known to be the most reactive aldehyde among the secondary of lipid peroxidation products. Therefore, the reaction products of y-TH with ONE have been investigated. When y-TH was reacted with ONE at 37℃ in the presence of HC1, product peaks 1-3 were detected by reversed-phase HPLC. Compounds 1-3 were isolated and their structures were determined by NMR. Compound 1 was determined to be 5- (1- (furan-2-yl) pentyl) -y-tocopherol, the addition product of y-TH with ONE. Compound 2 was also the addition product of y-TH with ONE where the C-5 position and 6-hydroxyl group of y-TH were bound to the C-5 and C-4 positions of ONE. Compound 3 was the addition product of γ-TH with two ONE molecules where the C-1 position of ONE residue in compound 2 was bound to the C-5 position of another ONE molecule. S-TH could also react with ONE to form some addition products although their structures were still unknown. The results indicate that y- and 8-THs which possess nucleophilic character in the chroman ring can act as scavengers of lipophilic electrophiles such as ONE.
y-TH is the major form of vitamin E in plant seeds and consequently in our diet. Thus, γ-TH may trap the membrane-soluble α,β-unsaturated aldehydes to form unreactive carbon-centered adducts before they can damage important biological molecules.

Report

(3 results)
  • 2007 Annual Research Report   Final Research Report Summary
  • 2006 Annual Research Report
  • Research Products

    (3 results)

All 2008

All Presentation (3 results)

  • [Presentation] ビタミンEと脂質過酸化二次生成物4-オキソ-2-ノネナールとの反応2008

    • Author(s)
      斉藤史恵、岩本悟志、山内 亮
    • Organizer
      日本農芸化学会2008年度大会
    • Place of Presentation
      名古屋
    • Year and Date
      2008-03-27
    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2007 Final Research Report Summary
  • [Presentation] ビタミンEと脂質過酸化二次生成物4-オキソ-2-ノネナールとの反応2008

    • Author(s)
      斉藤史恵、岩本悟志、山内 亮
    • Organizer
      日本農芸化学会
    • Place of Presentation
      名城大学(名古屋市)
    • Year and Date
      2008-03-27
    • Related Report
      2007 Annual Research Report
  • [Presentation] Reaction of vitamin E with the secondary products of lipid peroxidation, 4-oxo-2-nonenal2008

    • Author(s)
      Saito, F. Iwamoto, S. Yamauchi, R
    • Organizer
      Annual Meeting of JSBBA 2008
    • Place of Presentation
      Meijo University, Nagoya
    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2007 Final Research Report Summary

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Published: 2006-04-01   Modified: 2016-04-21  

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