Suzuki K, Nonaka K, Kono N, Ichihara K, Fukumoto Y, Inui Y, Miyagawa J, Onishi T, Hayashi C, Tarui S
Calcif Tissue Int. 1986 Nov;39(5):304-9. doi: 10.1007/BF02555195.
The effect of intravenous magnesium sulfate infusion on corrected serum calcium level and parathyroid function assessed by determination of nephrogenous cAMP (NcAMP) excretion were studied in normal human subjects. Significant hypermagnesemia induced by the magnesium sulfate infusion for 120 minutes was accompanied by a gradual and progressive decrease in the corrected serum calcium level. NcAMP excretion fell rapidly, reaching a nadir between 60 and 120 minutes after the infusion began, and after that rose above the baseline excretion. Urinary calcium excretion gradually increased, reaching a peak between 120 and 180 minutes after the infusion began and then gradually decreased. Since magnesium was given as the sulfate, it is not clear whether these changes were attributable to magnesium or sulfate or both. As a control study, we performed intravenous sodium sulfate infusion. The sodium sulfate infusion caused slight hypocalcemia, slight hypercalciuria, and a significant increase in NcAMP excretion. These findings indicate that the hypocalcemia and the hypercalciuria caused by the magnesium sulfate infusion is mainly due to the effect of magnesium, and that the decrease in NcAMP excretion during the infusion is due to the effect of magnesium alone. We conclude that the hypocalcemia caused by the magnesium sulfate infusion is mainly due to the renal calcium loss, and that the inhibition of parathyroid function caused by hypermagnesemia may be only partially involved in the early phase of this hypocalcemia.
在正常人体受试者中,研究了静脉输注硫酸镁对校正血清钙水平以及通过测定肾源性环磷酸腺苷(NcAMP)排泄来评估的甲状旁腺功能的影响。输注硫酸镁120分钟导致显著的高镁血症,同时校正血清钙水平逐渐且持续下降。NcAMP排泄迅速下降,在输注开始后60至120分钟达到最低点,之后又升至基线排泄水平之上。尿钙排泄逐渐增加,在输注开始后120至180分钟达到峰值,然后逐渐下降。由于给予的是硫酸镁,尚不清楚这些变化是归因于镁还是硫酸根或者两者皆有。作为对照研究,我们进行了静脉输注硫酸钠。输注硫酸钠导致轻度低钙血症、轻度高钙尿症以及NcAMP排泄显著增加。这些发现表明,硫酸镁输注引起的低钙血症和高钙尿症主要归因于镁的作用,输注期间NcAMP排泄的减少仅归因于镁的作用。我们得出结论,硫酸镁输注引起的低钙血症主要是由于肾钙丢失,高镁血症引起的甲状旁腺功能抑制可能仅部分参与了这种低钙血症的早期阶段。