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Zonal heterogeneity of the effects of chronic ethanol feeding on hepatic fatty acid metabolism

✍ Scribed by Manuel Guzman; Dr. José Castro


Publisher
John Wiley and Sons
Year
1990
Tongue
English
Weight
868 KB
Volume
12
Category
Article
ISSN
0270-9139

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✦ Synopsis


Periportal and perivenous hepatocytes were isolated from rats fed a high-fat, ethanol-containing diet to investigate the acinar heterogeneity of the effects of prolonged ethanol administration on lipid metabolism. Chronic feeding of ethanol caused a rather selective accumulation of triacylglycerols in the perivenous zone of the liver. In control animals the rate of lipgenesis and the activity of acetyl-CoA carboxylase were higher in perivenous than in periportal hepatocytes, whereas the rate of fatty acid oxidation and the activity of carnitine palmitoyltransferase I were higher in periportal than in perivenous cells, however, no zonation was evident for very-low-densitylipoprotein-lipid secretion. Prolonged ethanol administration abolished the zonal asymmetry of the lipogenic process and inverted the acinar distribution of the fatty acid-oxidative process (i.e., in ethanol-fed animals the rate of fatty acid oxidation and the activity of carnitine palmitoyltransferase I were higher in perivenous than in periportal hepatocytes). Moreover, chronic feeding of ethanol led to a marked and selective inhibition of very-low-deneity-lipoproteintriacylglycerol secretion by the perivenous zone of the liver. Nevertheless, no zonal differences were observed between control and ethanol-fed animals with respect to the effects of acute doses of ethanol and acetaldehyde on lipid metabolism. In conclusion, our results show that chronic ethanol intake produces important alterations in the acinar distribution of the different fatty acid-metabolizing pathways. (HEPATOLOGY 1990; 12:1O98-1105.)

The liver acinus may be divided in two different anatomical domains, namely an afferent, periportal zone and an efferent, perivenous zone ( 1, 2). These two liver regions display a marked phenotypical heterogeneity with regard to metabolic features and enzymatic equipment. Thus gluconeogenesis, fatty acid oxidation, and glycogen, urea and cholesterol synthesis are examples of


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