Planells E, Lerma A, Sánchez-Morito N, Aranda P, LLopis J
Institute of Nutrition and Food Technology, Department of Physiology, University of Granada, Spain.
J Am Coll Nutr. 1997 Aug;16(4):352-6. doi: 10.1080/07315724.1997.10718697.
The present study was undertaken to investigate the effect of dietary magnesium (Mg) deficiency on vitamin B2 (riboflavin) and B6 (pyridoxine) status in rats.
We fed Wistar rats an Mg-deficient diet (56 mg magnesium per kg food) for 70 days. On days 21, 35 and 70 we measured Mg and manganese (Mn) in plasma and whole blood, alkaline phosphatase in plasma, erythrocyte glutathione reductase activity coefficient (AC-EGR) for riboflavin status, and erythrocyte aspartase transaminase activity coefficient (AC-EAST) for vitamin B6 status.
Intake of the Mg-deficient diet significantly decreased plasma and whole blood levels of Mg and plasma alkaline phosphatase activity on all sampling days. The Mg deficit had no effect on plasma concentrations of Mn, but significantly increased whole blood levels of this element on days 35 and 70. The Mg-deficient diet had no effect on AC-EGR, and thus appeared not to affect riboflavin status. However, AC-EAST was significantly increased on day 70, implying that the animals were at risk for vitamin B6 deficiency.
Mg deficiency impairs vitamin B6 status by depleting intracellular Mg and thus inhibits the activity of alkaline phosphatase, a metalloenzyme required for the uptake of pyridoxal phosphate by tissues. Although part of the intraerythrocyte loss of Mg is countervailed by Mn, which can act as a substitute activator of alkaline phosphatase, the degree of compensation is insufficient to fully offset the decrease in activity caused by Mg depletion.
本研究旨在探讨膳食镁缺乏对大鼠维生素B2(核黄素)和B6(吡哆醇)状态的影响。
我们给Wistar大鼠喂食缺镁饮食(每千克食物含56毫克镁)70天。在第21天、35天和70天,我们测量了血浆和全血中的镁和锰、血浆碱性磷酸酶、用于评估核黄素状态的红细胞谷胱甘肽还原酶活性系数(AC-EGR)以及用于评估维生素B6状态的红细胞天冬氨酸转氨酶活性系数(AC-EAST)。
在所有采样日,摄入缺镁饮食均显著降低了血浆和全血中的镁水平以及血浆碱性磷酸酶活性。镁缺乏对血浆锰浓度没有影响,但在第35天和70天显著提高了全血中该元素的水平。缺镁饮食对AC-EGR没有影响,因此似乎不影响核黄素状态。然而,第70天AC-EAST显著升高,这意味着动物存在维生素B6缺乏的风险。
镁缺乏通过消耗细胞内镁来损害维生素B6状态,从而抑制碱性磷酸酶的活性,碱性磷酸酶是组织摄取磷酸吡哆醛所需的金属酶。尽管红细胞内镁的部分损失可被锰抵消,锰可作为碱性磷酸酶的替代激活剂,但补偿程度不足以完全抵消镁缺乏导致的活性降低。