Butterworth C E, Hatch K, Cole P, Sauberlich H E, Tamura T, Cornwell P E, Soong S J
Department of Nutrition Sciences, University of Alabama, Birmingham 35294.
Am J Clin Nutr. 1988 Mar;47(3):484-6. doi: 10.1093/ajcn/47.3.484.
It has been suggested that oral supplements of folic acid interfere with the intestinal absorption of zinc and may have toxic side effects. The concentrations of Zn and folate in blood were monitored in a group of women with cervical dysplasia randomly assigned to receive 10 mg/d of either folic acid (pteroylglutamic acid) or ascorbate. Fifty subjects were evaluated after 2 mo; 21 of the same subjects were evaluated again after 4 mo. No untoward clinical effects were observed. Significant elevation of erythrocyte folate above the baseline value was observed in the supplemented group but not in the placebo group (p less than 0.001). The concentration of Zn in plasma and erythrocytes did not change significantly in either the folate-treated or placebo groups after 2 and 4 mo. It is concluded that carefully controlled clinical intervention trials of this type do not impose a risk of depleting the concentration of Zn in erythrocytes and plasma.
有人提出,口服补充叶酸会干扰锌的肠道吸收,可能具有毒副作用。对一组患有宫颈发育异常的女性进行了监测,她们被随机分配接受每日10毫克的叶酸(蝶酰谷氨酸)或抗坏血酸。2个月后对50名受试者进行了评估;4个月后对其中21名相同的受试者再次进行了评估。未观察到不良临床影响。补充组的红细胞叶酸水平显著高于基线值,而安慰剂组则未出现这种情况(p<0.001)。叶酸治疗组和安慰剂组在2个月和4个月后,血浆和红细胞中的锌浓度均未发生显著变化。结论是,这种经过精心控制的临床干预试验不会有降低红细胞和血浆中锌浓度的风险。