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1
Research on alcohol metabolism among Asians and its implications for understanding causes of alcoholism.亚洲人酒精代谢研究及其对理解酗酒原因的启示。
Public Health Rep. 1989 Nov-Dec;104(6):615-20.
2
The role of alcohol dehydrogenase and aldehyde dehydrogenase isozymes in alcohol metabolism, alcohol sensitivity, and alcoholism.乙醇脱氢酶和乙醛脱氢酶同工酶在酒精代谢、酒精敏感性及酒精中毒中的作用。
Isozymes Curr Top Biol Med Res. 1983;8:175-93.
3
Alcohol dehydrogenase: enzymology and metabolism.乙醇脱氢酶:酶学与代谢
Alcohol Alcohol Suppl. 1994;2:113-9.
4
Alcohol dehydrogenase (ADH) and aldehyde dehydrogenase (ALDH) in the cancer diseases.癌症疾病中的乙醇脱氢酶(ADH)和乙醛脱氢酶(ALDH)。
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Polymorphism of ethanol-metabolism genes and alcoholism: correlation of allelic variations with the pharmacokinetic and pharmacodynamic consequences.乙醇代谢基因多态性与酒精中毒:等位基因变异与药代动力学和药效学后果的相关性
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Expression pattern, ethanol-metabolizing activities, and cellular localization of alcohol and aldehyde dehydrogenases in human large bowel: association of the functional polymorphisms of ADH and ALDH genes with hemorrhoids and colorectal cancer.在人类大肠中,醇脱氢酶和醛脱氢酶的表达模式、乙醇代谢活性和细胞定位:ADH 和 ALDH 基因的功能多态性与痔疮和结直肠癌的关系。
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Differences in pharmacogenetics of nicotine and alcohol metabolism: review and recommendations for future research.尼古丁与酒精代谢的药物遗传学差异:综述及对未来研究的建议
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Expression pattern, ethanol-metabolizing activities, and cellular localization of alcohol and aldehyde dehydrogenases in human small intestine.人小肠中醇脱氢酶和醛脱氢酶的表达模式、乙醇代谢活性和细胞定位。
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Alcohol Res Health. 2007;30(1):5-13.

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Phosphatidylethanol and self-reported alcohol consumption among people living with HIV in Thai Nguyen, Vietnam.越南谅山地区艾滋病毒感染者的磷脂酰乙醇与自我报告的饮酒情况
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Clinical profile and prognostic factors of alcoholic cardiomyopathy in tribal and non-tribal population.酒精性心肌病在部落和非部落人群中的临床特征和预后因素。
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The neuronal nitric oxide synthase (nNOS) gene and neuroprotection against alcohol toxicity.神经元型一氧化氮合酶(nNOS)基因与针对酒精毒性的神经保护作用。
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Reasons for Substance Use: A Comparative Study of Alcohol Use in Tribals and Non-tribals.物质使用的原因:部落居民与非部落居民酒精使用的比较研究
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Improving the health of minorities.改善少数群体的健康状况。
Public Health Rep. 1989 Nov-Dec;104(6):523-5.

本文引用的文献

1
Genetic determinants of alcohol and aldehyde dehydrogenases and alcohol metabolism.酒精脱氢酶、乙醛脱氢酶与酒精代谢的遗传决定因素
Semin Liver Dis. 1981 Aug;1(3):179-88. doi: 10.1055/s-2008-1041746.
2
Identification of fatty acid ethyl esters as products of rabbit myocardial ethanol metabolism.
J Biol Chem. 1981 Dec 25;256(24):12968-73.
3
New human liver alcohol dehydrogenase forms with unique kinetic characteristics.具有独特动力学特性的新型人类肝脏乙醇脱氢酶形式。
Biochem Biophys Res Commun. 1981 Jan 15;98(1):122-30. doi: 10.1016/0006-291x(81)91878-7.
4
New molecular forms of human liver alcohol dehydrogenase: isolation and characterization of ADHIndianapolis.人肝脏乙醇脱氢酶的新分子形式:印第安纳波利斯ADH的分离与特性鉴定
Proc Natl Acad Sci U S A. 1980 Oct;77(10):5784-8. doi: 10.1073/pnas.77.10.5784.
5
Electrophoretic and biochemical studies of human aldehyde dehydrogenase isozymes in various tissues.人体不同组织中醛脱氢酶同工酶的电泳及生化研究。
Life Sci. 1980 May 26;26(21):1773-80. doi: 10.1016/0024-3205(80)90577-9.
6
Population genetic studies on aldehyde dehydrogenase isozyme deficiency and alcohol sensitivity.关于醛脱氢酶同工酶缺乏与酒精敏感性的群体遗传学研究。
Am J Hum Genet. 1983 Jul;35(4):769-72.
7
Determination of genotypes of human aldehyde dehydrogenase ALDH2 locus.人类乙醛脱氢酶ALDH2基因座基因型的测定
Am J Hum Genet. 1983 Nov;35(6):1107-16.
8
Thermodynamic bases for fatty acid ethyl ester synthase catalyzed esterification of free fatty acid with ethanol and accumulation of fatty acid ethyl esters.脂肪酸乙酯合酶催化游离脂肪酸与乙醇酯化反应及脂肪酸乙酯积累的热力学基础。
Biochemistry. 1984 Aug 28;23(18):4082-7. doi: 10.1021/bi00313a011.
9
The effects of alcohol on carbohydrate metabolism.酒精对碳水化合物代谢的影响。
Contemp Issues Clin Biochem. 1984;1:135-48.
10
Human liver alcohol dehydrogenase: purification and kinetic characterization of the beta 2 beta 2, beta 2 beta 1, alpha beta 2, and beta 2 gamma 1 "Oriental" isoenzymes.人肝脏乙醇脱氢酶:β2β2、β2β1、αβ2和β2γ1“东方型”同工酶的纯化及动力学特性研究
Biochemistry. 1984 Nov 20;23(24):5847-53. doi: 10.1021/bi00319a026.

亚洲人酒精代谢研究及其对理解酗酒原因的启示。

Research on alcohol metabolism among Asians and its implications for understanding causes of alcoholism.

作者信息

Suddendorf R F

机构信息

National Institute on Alcohol Abuse and Alcoholism, Rockville, MD 20857.

出版信息

Public Health Rep. 1989 Nov-Dec;104(6):615-20.

PMID:2511595
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1580147/
Abstract

Research into the causes of alcoholism is a relatively recent scientific endeavor. One area of study which could lead to better understanding of the disease is the possibility of a genetic predisposition to alcoholism. Recent work has demonstrated that people have varying complements of enzymes to metabolize alcohol. Current knowledge is examined about the influence of various ethanol metabolizing enzymes on alcohol consumption by Asians and members of other ethnic groups. The two principal enzymes involved in ethanol oxidative metabolism are alcohol dehydrogenase (ADH) and aldehyde dehydrogenase (ALDH). ADH is responsible for the metabolism of ethanol to acetaldehyde. ALDH catalyzes the conversion of acetaldehyde to acetate. The different isozymes account for the diversity of alcohol metabolism among individuals. An isozyme of ADH (beta 2 beta 2) is found more frequently in Asians than in whites, and an ALDH isozyme (ALDH2), although present in Asians, often is in an inactive form. The presence of an inactive form of ALDH2 is thought to be responsible for an increase in acetaldehyde levels in the body. Acetaldehyde is considered responsible for the facial flushing reaction often observed among Asians who have consumed alcohol. A dysphoric reaction to alcohol, producing uncomfortable sensations, is believed to be a response to deter further consumption. Although the presence of an inactive ALDH2 isozyme may serve as a deterrent to alcohol consumption, its presence does not fully explain the levels of alcohol consumption by those with the inactive isozyme. Other conditions, such as social pressure, and yet undetermined biological factors, may play a significant role in alcohol consumption.

摘要

对酒精中毒原因的研究是一项相对较新的科学尝试。一个可能有助于更好理解这种疾病的研究领域是酒精中毒的遗传易感性。最近的研究表明,人们代谢酒精的酶的组成各不相同。本文探讨了目前关于各种乙醇代谢酶对亚洲人和其他种族群体饮酒影响的认识。参与乙醇氧化代谢的两种主要酶是乙醇脱氢酶(ADH)和乙醛脱氢酶(ALDH)。ADH负责将乙醇代谢为乙醛。ALDH催化乙醛转化为乙酸。不同的同工酶导致了个体间酒精代谢的差异。ADH的一种同工酶(β2β2)在亚洲人中比在白人中更常见,而一种ALDH同工酶(ALDH2)虽然在亚洲人中存在,但通常处于无活性状态。ALDH2无活性形式的存在被认为是导致体内乙醛水平升高的原因。乙醛被认为是导致饮酒后的亚洲人经常出现脸红反应的原因。对酒精产生烦躁反应,产生不适感,被认为是一种阻止进一步饮酒的反应。虽然无活性的ALDH2同工酶的存在可能会抑制饮酒,但它的存在并不能完全解释携带这种无活性同工酶的人的饮酒量。其他因素,如社会压力和尚未确定的生物学因素,可能在饮酒中起重要作用。