Cited by 148Alcohol Consumption and Health EffectsSubstance Abuse Treatment and OutcomesAlcoholism and Thiamine Deficiency

Determinants of Blood Acetaldehyde Level during Ethanol Oxidation in Chronic Alcoholics

Nuutinen, Hannu, Lindros, Kai O., Salaspuro, Mikko·1983·Alcoholism: Clinical and Experimental Research

Abstract

We analyzed the blood alcohol and acetaldehyde concentrations in nine alcoholics and four healthy nonalcoholic controls during and after an intravenous infusion of a high and a low dose of alcohol. In the alcoholics, the mean rates of plasma ethanol disappearance were significantly higher than in nonalcoholic controls. In the control subjects, the blood acetaldehyde levels were, in general, below the detection limit (less than 0.5 microM), but in sharp contrast to this, an elevated blood acetaldehyde during ethanol infusion was found in 6/9 alcoholics. Peak blood acetaldehyde values were higher after the high than the low dose of alcohol. Fructose infusion significantly enhanced the rate of plasma ethanol disappearance both in controls and in alcoholics, and this was usually associated with a significant elevation of blood acetaldehyde level. The maximal specific activities (expressed as milliunits/mg og protein) of alcohol, lactate, and aldehyde dehydrogenases in liver were significantly lower in alcoholics than in controls. Even more importantly, the peak blood acetaldehyde correlated negatively with the activity of hepatic "low-Km" aldehyde dehydrogenase. Our results suggest that the main reason for blood acetaldehyde elevation seen in these chronic alcoholics is their impaired capacity to metabolize acetaldehyde. This may be further accentuated by the increased rate of ethanol oxidation.

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Crossref · 10.1111/j.1530-0277.1983.tb05432.x

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  • In human ALD, blood acetaldehyde level is significantly upregulated and its increase parallels the elevation of ethanol concentration.

    “In human ALD, blood acetaldehyde level is significantly upregulated and its increase parallels the elevation of ethanol concentration [140,141,142,143].”

    From Pathophysiological Aspects of Alcohol Metabolism in the Liver (2021) · cites this paper as [143]

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Authors
Nuutinen, H., Lindros, K. O., & Salaspuro, M.
Affiliations
University of Helsinki (FI)
Corresponding author
Salaspuro, Mikko
Venue
Alcoholism: Clinical and Experimental Research
Publisher
Wiley
Published
1983-03
Volume
7
Issue
2
Pages
163-168
ISSN
  • 0145-6008 (ISSN-L)
  • 1530-0277
OpenAlex
W2026836582
Cited by
148
References
0
Citations by year
2025: 2 · 2023: 1 · 2022: 1 · 2021: 3 · 2020: 1 · 2019: 3 · 2018: 2 · 2017: 1 · 2016: 3 · 2015: 4 · 2014: 3 · 2013: 2 · 2012: 4
FWCI
7.15
Type
journal article
Language
en
Open access
closed
Locations
  • Alcoholism Clinical and Experimental Research (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Pathology and Forensic Medicine › Alcohol Consumption and Health Effects
  • Health Sciences › Medicine › Epidemiology › Substance Abuse Treatment and Outcomes
  • Health Sciences › Medicine › Neurology › Alcoholism and Thiamine Deficiency
Keywords
blood acetaldehyde, chronic alcoholism, ethanol oxidation, acetaldehyde dehydrogenase, fructose, hepatic enzyme activity, alcohol metabolism
MeSH terms
Acetaldehyde, Adult, Alcohol Oxidoreductases, Ethanol, Alcoholism, Aldehyde Oxidoreductases, Fructose, Humans, Liver, Male, Middle Aged

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