Ethanol feeding enhances age-related deterioration of the rat hepatic mitochondrion

被引:18
作者
Cahill, A [1 ]
Hershman, S [1 ]
Davies, A [1 ]
Sykora, P [1 ]
机构
[1] Thomas Jefferson Univ, Dept Pathol Anat & Cell Biol, Philadelphia, PA 19107 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY | 2005年 / 289卷 / 06期
关键词
mitochondrial DNA; respiration; polymerase-blocking lesions; citrate synthase;
D O I
10.1152/ajpgi.00193.2005
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Chronic ethanol feeding damages the hepatic mitochondrion by increasing mitochondrial DNA ( mtDNA) oxidation, lowering mtDNA yields and impairing mitochondrial respiration. These effects are also seen during aging. By employing a 21-day chronic feeding regimen, we investigated the effects of ethanol consumption on mtDNA content and mitochondrial respiration in 2-, 12-, and 24-mo-old male rats. Aging resulted in decreased mtDNA content, increased mtDNA damage ( as indicated by inhibition of Taq polymerase progression), and a decline in state 3 respiration; effects that were further exacerbated by ethanol feeding. Additionally, ethanol consumption caused an increase in the levels of citrate synthase while not impacting mitochondrial protein content. In conclusion, ethanol and aging combine to cause deterioration in the structural and functional integrity of the hepatic mitochondrion. The additive effects of aging and ethanol feeding may have serious consequences for hepatic energy metabolism in aged animals, and their detrimental combination may serve as one of the molecular mechanisms underlying the progression of alcoholic liver disease.
引用
收藏
页码:G1115 / G1123
页数:9
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