Halsted Charles H, Villanueva Jesus A, Devlin Angela M, James S Jill
University of California, Davis, California and National Toxicological Research Center, Jefferson, Arkansas, USA.
Trans Am Clin Climatol Assoc. 2002;113:151-62; discussion 162-3.
Folate deficiency is present in most patients with alcoholic liver disease (ALD), whereas folate regulates and alcoholism perturbs intrahepatic methionine metabolism, and S-adenosyl-methionine prevents the development of experimental ALD. Our studies explored the hypothesis that abnormal methionine metabolism is exacerbated by folate deficiency and promotes the development of ALD in the setting of chronic ethanol exposure. Using the micropig animal model, dietary combinations of folate deficiency and a diet containing 40% of kcal as ethanol were followed by measurements of hepatic methionine metabolism and indices of ALD. Alcoholic liver injury, expressed as steatohepatitis in terminal 14 week liver specimens, was evident in micropigs fed the combined ethanol containing and folate deficient diet but not in micropigs fed each diet separately. Perturbations of methionine metabolism included decreased hepatic S-adenosylmethionine and glutathione with increased products of DNA and lipid oxidation. Thus, the development of ALD is linked to abnormal methionine metabolism and is accelerated in the presence of folate deficiency.
大多数酒精性肝病(ALD)患者存在叶酸缺乏,而叶酸调节且酗酒扰乱肝内蛋氨酸代谢,S-腺苷甲硫氨酸可预防实验性ALD的发生。我们的研究探讨了以下假说:在慢性乙醇暴露情况下,叶酸缺乏会加剧蛋氨酸代谢异常,并促进ALD的发展。使用小型猪动物模型,采用叶酸缺乏饮食与含40%千卡乙醇的饮食组合,随后测量肝蛋氨酸代谢和ALD指标。在喂食含乙醇和叶酸缺乏组合饮食的小型猪中,在第14周末期肝脏标本中表现为脂肪性肝炎的酒精性肝损伤很明显,但在分别喂食每种饮食的小型猪中则不明显。蛋氨酸代谢紊乱包括肝脏S-腺苷甲硫氨酸和谷胱甘肽减少,DNA和脂质氧化产物增加。因此,ALD的发展与蛋氨酸代谢异常有关,并且在叶酸缺乏的情况下会加速。