Min Hyesun, Im Eun-Sun, Seo Jung-Sook, Mun Ju Ae, Burri Betty J
Department of Food and Nutrition, Hannam University, Daejeon, Korea.
Alcohol Clin Exp Res. 2005 Dec;29(12):2188-93. doi: 10.1097/01.alc.0000191756.02856.a8.
We recently observed that ethanol feeding impairs 10-formyltetrahydrofolate (10-FTHF) dehydrogenase (EC 1.5.1.6.) and 10-FTHF hydrolase activity in rats. In the present study, we explored the effects of folate deficiency or sufficiency combined with alcoholic intake on 10-FTHF and possible mechanisms by which chronic ethanol ingestion produces folate deficiency.
Sprague-Dawley rats were fed either folate-sufficient (FS) or folate-deficient (FD) diets; with or without ethanol (E) for four weeks. Hepatic 10-FTHF dehydrogenase and hydrolase activity, plasma folate and homocysteine were measured at baseline and after feeding experimental diets.
Liver weight increased slightly with either folate deficiency or ethanol consumption. In rats fed the folate-sufficient diet with ethanol (FSE), plasma folate was decreased slightly (p<0.05) and plasma homocysteine elevated compared to rats fed the FS diet without ethanol. Ethanol did not affect plasma folate and plasma homocysteine in FD rats. Red-blood cell (RBC) folate was increased similarly in rats by ethanol feeding (FSE and FDE>FS and FD). Feeding folate deficient or ethanol (FSE, FD and FDE) diets depressed hepatic activities of 10-FTHF dehydrogenase, which catalyzes the oxidative deformylation of 10-FTHF to tetrahydrofolate (THF) and carbon dioxide. Rats consuming the FDE diet had the lowest enzyme activities of the experimental groups, implying that folate deficiency and ethanol consumption each affect enzyme activity.
We confirm that ethanol decreases hepatic 10-FTHF dehydrogenase activity and show that this decrease occurs irrespective of folate status. This shows that modulation of 10-FTHF is one possible mechanism by which ethanol intake decreases folate status and affects one-carbon metabolism.
我们最近观察到,给大鼠喂食乙醇会损害10-甲酰四氢叶酸(10-FTHF)脱氢酶(EC 1.5.1.6.)和10-FTHF水解酶的活性。在本研究中,我们探讨了叶酸缺乏或充足与酒精摄入相结合对10-FTHF的影响,以及慢性乙醇摄入导致叶酸缺乏的可能机制。
将斯普拉格-道利大鼠分为叶酸充足(FS)或叶酸缺乏(FD)饮食组;分别给予或不给予乙醇(E),持续四周。在喂食实验饮食前后的基线期测量肝脏10-FTHF脱氢酶和水解酶活性、血浆叶酸和同型半胱氨酸水平。
叶酸缺乏或乙醇摄入均使肝脏重量略有增加。与喂食不含乙醇的FS饮食的大鼠相比,喂食含乙醇的叶酸充足饮食(FSE)的大鼠血浆叶酸略有降低(p<0.05),血浆同型半胱氨酸升高。乙醇对FD大鼠的血浆叶酸和血浆同型半胱氨酸没有影响。乙醇喂养使大鼠红细胞(RBC)叶酸同样增加(FSE和FDE>FS和FD)。喂食叶酸缺乏或乙醇(FSE、FD和FDE)饮食会降低肝脏10-FTHF脱氢酶的活性,该酶催化10-FTHF氧化脱甲酰基生成四氢叶酸(THF)和二氧化碳。食用FDE饮食的大鼠在实验组中酶活性最低,这意味着叶酸缺乏和乙醇摄入各自都会影响酶活性。
我们证实乙醇会降低肝脏10-FTHF脱氢酶的活性,并表明这种降低与叶酸状态无关。这表明10-FTHF的调节是乙醇摄入降低叶酸状态并影响一碳代谢的一种可能机制。