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Alcohol reduces MMP-2 in humans and isolated smooth muscle cells.

FIOTTI, NICOLA
•
TUBARO F
•
ALTAMURA N
altro
GIANSANTE, CARLO
2008
  • journal article

Periodico
ALCOHOL
Abstract
Alcoholic beverages are known to exert a protective effect on atherosclerotic disease. This study aimed to assess the in vivo and in vitro effects of alcohol on matrix metalloproteinase (MMP) -2 and -9, known to determine atherosclerosis progression. Eighteen healthy volunteers, regular drinkers (two standard alcohol servings/day, on average) at first examination (baseline) were asked to abstain from any alcoholic beverage for one week (abstention), and then to assume two standard alcohol servings of beer daily for 1 week (re-exposure). Activity of MMP-2 and -9, total antioxidant activity (AOA), glutathione (GSH) plasma levels were carried out at baseline, at the end of abstention, and after 1 week of re-exposure. To validate the in vivo results, MMP-2 activity and expression, AOA, and GSH, were determined in human smooth muscle cells treated for 96 h with increasing concentrations (12.5e100 mM) of ethanol. MMP-2, but not MMP-9 plasma activity was higher at abstention than at baseline or re-exposure (P!.001 and P#.005, respectively). Changes in AOA and GSH throughout the study were not significant. No correlation was found between MMPs and antioxidant activity. In vitro, ethanol at 25 mM reduced by around 10% MMP-2 activity (P5.003) in smooth muscle cells, whereas MMP-2 expression, AOA, and GSH were unaffected. Alcohol reduces MMP-2 plasma activity in healthy humans and in isolated vascular smooth muscle cells. This in vitro reduction is unrelated to MMP-2 expression in vascular cells or to antioxidant levels changes.
DOI
10.1016/j.alcohol.2008.02.001
WOS
WOS:000258012900006
Archivio
http://hdl.handle.net/11368/1848349
info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-46449098338
Diritti
metadata only access
Soggetti
  • matrix metalloprotein...

  • smooth muscle cell

  • Antioxidant activity

  • Ethanol

Web of Science© citazioni
12
Data di acquisizione
Mar 22, 2024
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