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2015 Fiscal Year Final Research Report

The roles of high Km ADH3 on alcohol metabolism and alcoholc disorders under chronic alcohol comsumpsion

Research Project

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Project/Area Number 25460879
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Legal medicine
Research InstitutionNippon Medical School

Principal Investigator

Haseba Takeshi  日本医科大学, 医学部, 准教授 (50156329)

Co-Investigator(Kenkyū-buntansha) AKIMOTO Toshio  日本医科大学, 医学部, 准教授 (30184112)
MARUYAMA Motoyo  日本医科大学, 医学部, 助教 (60709757)
Project Period (FY) 2013-04-01 – 2016-03-31
Keywordsアルコール代謝 / ADH1 / ADH3 / アルコール嗜好性 / アルコール肝障害 / アルコール依存 / ノックアウトマウス / 慢性アルコール摂取
Outline of Final Research Achievements

Three kinds of mice with different ADH genotypes(Wild, Adh1-/-, Adh3-/-) were subjected under chronic alcohol consumption(CAC) with 10% ethanol. ADH1 was found to be indispensable to continue CAC, and to have protective roles in alcoholic liver disease and dependence. On the other hand, ADH3 was demonstrated to accelerate alcoholic liver disease and alcoholism, although it represses daily alcohol intake under CAC. It is also suggested that both ADHs contribute to an increase in alcohol metabolism by CAC, especially in the absence of the other one, however, the contribution of ADH1 decrease in the prolonged CAC, differing from that of ADH3.

Free Research Field

法医学

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Published: 2017-05-10  

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