Milne M L, Baran D T
Calcif Tissue Int. 1985 Jan;37(1):77-81. doi: 10.1007/BF02557683.
Acute metabolic acidosis alters 1,25 dihydroxyvitamin D metabolism in experimental animals. We have used the NH4Cl-treated rachitic rat as a model to investigate the effect of acidosis on hepatic 25 hydroxyvitamin D (25 OHD) production. NH4Cl ingestion for 4 days was associated with a significant decrease in blood pH (7.44 +/- 0.03 vs 7.17 +/- 0.03, P less than 0.001) and bicarbonate (22.2 +/- 0.9 vs 10.5 +/- 1.6 mEq/liter, P less than 0.001). Acute metabolic acidosis stimulated 3H-25 hydroxyvitamin D production in liver homogenates. Acidosis resulted in a 52% decrease in Km (50.9 nM vs 24.5 nM) and an 11% decrease in the Vmax (554 picomoles/g liver protein/3 h vs 491 picomoles/g liver protein/3 h). The data collectively suggest that an acid load in vivo increases hepatic 25 OHD production and apparently enhances enzyme affinity for substrate.
急性代谢性酸中毒会改变实验动物体内1,25-二羟基维生素D的代谢。我们使用氯化铵处理的佝偻病大鼠作为模型,来研究酸中毒对肝脏25-羟基维生素D(25-OHD)生成的影响。摄入氯化铵4天与血液pH值显著降低(7.44±0.03对7.17±0.03,P<0.001)和碳酸氢盐降低(22.2±0.9对10.5±1.6 mEq/升,P<0.001)相关。急性代谢性酸中毒刺激了肝脏匀浆中3H-25-羟基维生素D的生成。酸中毒导致米氏常数(Km)降低52%(50.9 nM对24.5 nM),最大反应速度(Vmax)降低11%(554皮摩尔/克肝脏蛋白/3小时对491皮摩尔/克肝脏蛋白/3小时)。这些数据共同表明,体内的酸负荷会增加肝脏25-OHD的生成,并且明显增强酶对底物的亲和力。