Setoue Minoru, Ohuchi Seiya, Morita Tatsuya, Sugiyama Kimio
Department of Applied Biological Chemistry, Faculty of Agriculture, Shizuoka University, Shizuoka, Japan.
J Nutr Sci Vitaminol (Tokyo). 2008 Dec;54(6):483-90. doi: 10.3177/jnsv.54.483.
To clarify the relationship between dietary choline level and plasma homocysteine concentration, the effects of choline deprivation on plasma homocysteine concentration and related variables were investigated in rats fed a standard (25%) casein (25C) diet or standard soybean protein (25S) diet. Using the 25S diet, the time-dependent effect of choline deprivation and the comparative effects of three kinds of lipotropes were also investigated. Feeding rats with the choline-deprived 25S diet for 10 d significantly increased plasma total homocysteine concentration to a level 2.68-times higher than that of the control group, whereas choline deprivation had no effect in rats fed the 25C diet. Increases in hepatic S-adenosylhomocysteine and homocysteine concentrations, decreases in hepatic betaine concentration and the activity of cystathionine beta-synthase, but not betaine-homocysteine S-methyltransferase, and fatty liver also occurred in rats fed the choline-deprived 25S diet. Plasma homocysteine concentration increased when rats were fed the choline-deprived 25S diet for only 3 d, and the increase persisted up to 20 d. The hyperhomocysteinemia induced by choline deprivation was effectively suppressed by betaine or methionine supplementation. Choline deprivation caused hyperhomocysteinemia also in rats fed a choline-deprived low (10%) casein diet. The results indicate that choline deprivation can easily induce prominent hyperhomocysteinemia when rats are fed relatively low methionine diets such as a standard soybean protein diet and low casein diet, possibly through the suppression of homocysteine removal by both remethylation and cystathionine formation. This hyperhomocysteinemia might be a useful model for investigating the role of betaine in the regulation of plasma homocysteine concentration.
为阐明膳食胆碱水平与血浆同型半胱氨酸浓度之间的关系,在喂食标准(25%)酪蛋白(25C)饮食或标准大豆蛋白(25S)饮食的大鼠中,研究了胆碱缺乏对血浆同型半胱氨酸浓度及相关变量的影响。采用25S饮食,还研究了胆碱缺乏的时间依赖性效应以及三种抗脂肪肝物质的比较效应。给大鼠喂食胆碱缺乏的25S饮食10天,可使血浆总同型半胱氨酸浓度显著升高至对照组的2.68倍,而胆碱缺乏对喂食25C饮食的大鼠没有影响。喂食胆碱缺乏的25S饮食的大鼠还出现肝脏S-腺苷同型半胱氨酸和同型半胱氨酸浓度升高、肝脏甜菜碱浓度降低、胱硫醚β-合酶活性降低(但甜菜碱-同型半胱氨酸S-甲基转移酶活性未降低)以及脂肪肝。大鼠仅喂食胆碱缺乏的25S饮食3天,血浆同型半胱氨酸浓度就会升高,且这种升高持续至20天。补充甜菜碱或蛋氨酸可有效抑制胆碱缺乏诱导的高同型半胱氨酸血症。胆碱缺乏在喂食胆碱缺乏的低(10%)酪蛋白饮食的大鼠中也会导致高同型半胱氨酸血症。结果表明,当给大鼠喂食相对低蛋氨酸饮食(如标准大豆蛋白饮食和低酪蛋白饮食)时,胆碱缺乏可能通过抑制同型半胱氨酸的再甲基化和胱硫醚形成来清除同型半胱氨酸,从而容易诱导显著的高同型半胱氨酸血症。这种高同型半胱氨酸血症可能是研究甜菜碱在调节血浆同型半胱氨酸浓度中的作用的有用模型。