Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
11
pubmed:dateCreated
1997-12-8
pubmed:abstractText
We have recently shown that a large amount of wine (750 mL, approximately 70 g of alcohol) markedly impairs postprandial hepatic protein metabolism in healthy subjects. This is probably due to the shift in the intracellular redox state (increased NADH/NAD+) induced by ethanol oxidation. If this hypothesis is true, the administration of nicotinamide (NAD+ precursor) should provide NAD+ in excess and thus correct the NADH/NAD+ abnormalities and prevent the ethanol hepatotoxicity. Whole-body protein metabolism and the fractional secretory rates of hepatic (albumin, fibrinogen) and extra-hepatic (immunoglobulin G, IgG) plasma proteins were measured in the basal postabsorptive and in the absorptive states in 15 healthy subjects, that had been assigned to three groups matched for age and body mass index. During the absorptive state (intragastric meal), the three groups received water (control), 750 mL of wine, or 750 mL of wine + 1.25 g of nicotinamide, respectively. The redox state was estimated by determining the plasma lactate/pyruvate ratio. Compared with the basal state, wine alone increased the lactate/pyruvate ratio twofold and depressed the fractional secretory rates of albumin and fibrinogen (P < 0.01 vs. control and nicotinamide); nicotinamide reduced the effects of wine on the lactate/pyruvate ratio (P < 0.02 vs. wine alone) and prevented the reduction of albumin and fibrinogen secretory rates (P > 0.05 vs. control). These results indicate that nicotinamide counteracts the acute hepatotoxic effects of ethanol by ameliorating the redox state.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0022-3166
pubmed:author
pubmed:issnType
Print
pubmed:volume
127
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2199-204
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:9349848-Adult, pubmed-meshheading:9349848-Albumins, pubmed-meshheading:9349848-Alcohol Drinking, pubmed-meshheading:9349848-Blood Glucose, pubmed-meshheading:9349848-Body Mass Index, pubmed-meshheading:9349848-Drug Interactions, pubmed-meshheading:9349848-Ethanol, pubmed-meshheading:9349848-Female, pubmed-meshheading:9349848-Fibrinogen, pubmed-meshheading:9349848-Humans, pubmed-meshheading:9349848-Immunoglobulin G, pubmed-meshheading:9349848-Insulin, pubmed-meshheading:9349848-Lactates, pubmed-meshheading:9349848-Leucine, pubmed-meshheading:9349848-Liver, pubmed-meshheading:9349848-Male, pubmed-meshheading:9349848-NAD, pubmed-meshheading:9349848-Niacinamide, pubmed-meshheading:9349848-Oxidation-Reduction, pubmed-meshheading:9349848-Proteins, pubmed-meshheading:9349848-Pyruvates
pubmed:year
1997
pubmed:articleTitle
Nicotinamide counteracts alcohol-induced impairment of hepatic protein metabolism in humans.
pubmed:affiliation
Department of Internal Medicine, Endocrine and Metabolic Sciences, University of Perugia, 06126 Perugia, Italy.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't