Modulation of ethanol effect on hepatocyte proliferation by polyamines

被引:10
作者
Do, T. H. T. [1 ,2 ]
Gaboriau, F. [1 ,2 ]
Morel, I. [2 ,3 ]
Lepage, S. [3 ]
Cannie, I. [1 ,2 ]
Loreal, O. [1 ,2 ]
Lescoat, G. [1 ,2 ]
机构
[1] Hop Pontchaillou, INSERM, UMR 991, F-35033 Rennes, France
[2] Univ Rennes 1, Rennes, France
[3] CHU Rennes, Lab Toxicol Biol & Medicolegale, Rennes, France
关键词
Ethanol; Hepatocyte; Cell proliferation; Polyamine metabolism; A-difluoromethyl ornithine; ORNITHINE-DECARBOXYLASE ACTIVITY; GAMMA-AMINOBUTYRIC-ACID; HEPATITIS-B-VIRUS; CELL-LINE; PARTIAL-HEPATECTOMY; LIVER-REGENERATION; MASS-SPECTROMETRY; DIFFERENTIATION; INHIBITION; RATS;
D O I
10.1007/s00726-012-1413-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
An occurrence and a magnitude of alcoholic liver diseases depend on the balance between ethanol-induced injury and liver regeneration. Like ethanol, polyamines including putrescine, spermidine, and spermine modulate cell proliferation. Thus, the purpose of this study was to evaluate the relationship between effect of ethanol on hepatocyte (HC) proliferation and polyamine metabolism using the HepaRG cell model. Results showed that ethanol effect in proliferating HepaRG cells was associated with a decrease in intracellular polyamine levels and ornithine decarboxylase (ODC) activity. Ethanol also induced disorders in expression of genes coding for polyamine-metabolizing enzymes. The alpha-difluoromethyl ornithine, an irreversible inhibitor of ODC, amplified ethanol toxicity on cell viability, protein level, and DNA synthesis through accentuation of polyamine depletion in proliferating HepaRG cells. Conversely, putrescine reversed ethanol effect on cell proliferation parameters. In conclusion, this study suggested that ethanol effect on HC proliferation was closely related to polyamine metabolism and that manipulation of this metabolism by putrescine could protect against the anti-proliferative activity of ethanol.
引用
收藏
页码:869 / 877
页数:9
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