Milne D B, Omaye S T
Int J Vitam Nutr Res. 1980;50(3):301-8.
Although interaction of vitamin C, copper and iron have been studied in several species, little is known about these interactions in species which require the vitamin in the diet. Young male Hartley guinea pigs were fed a basal diet, or a basal diet and supplemented daily with vitamin C, p.o. Pharmacologic doses (25 mg per 100 g BW per day) of vitamin C resulted in two-to-three-fold decreases in liver copper, when compared with those receiving normal (0.5 mg per 100 g BW per day) intakes. Under conditions of vitamin C deficiency, serum copper and ceruloplasmin were elevated along with liver copper. Serum and hepatic iron levels, hepatic microsomal cytochrome P-450 and cytochrome b5, and blood heme parameters all appeared to be directly related to vitamin C intake, i.e. the iron and heme parameters increased as the vitamin dose increased. These data are consistent with the hypothesis that interaction between vitamin C, copper and iron influence normal heme formation through the oxidation/reduction of iron and/or by regulating iron absorption and availability at the gut level.
尽管已经在多个物种中研究了维生素C、铜和铁之间的相互作用,但对于那些需要从饮食中获取该维生素的物种,这些相互作用仍知之甚少。给年轻雄性哈特利豚鼠喂食基础日粮,或喂食基础日粮并每日口服补充维生素C。与摄入正常量(每天每100克体重0.5毫克)维生素C的豚鼠相比,药理剂量(每天每100克体重25毫克)的维生素C可使肝脏铜含量降低两到三倍。在维生素C缺乏的情况下,血清铜和铜蓝蛋白以及肝脏铜含量均会升高。血清和肝脏铁水平、肝脏微粒体细胞色素P-450和细胞色素b5以及血液血红素参数似乎都与维生素C摄入量直接相关,即随着维生素剂量增加,铁和血红素参数也会增加。这些数据与以下假设一致:维生素C与铜和铁之间的相互作用通过铁的氧化/还原和/或通过调节肠道水平的铁吸收及可利用性来影响正常血红素的形成。