Kimura Y, Nakayama M, Kuriyama S, Watanabe S, Kawaguchi Y, Sakai O
Department of Internal Medicine, Jikei University School of Medicine, Kashiwa Hospital, Chiba, Japan.
Clin Nephrol. 1991 Feb;35(2):72-7.
Two active forms of vitamin D3, 1 alpha, 25-dihydroxyvitamin D3 (1 alpha, 25 [OH] 2D3) and 1 alpha-hydroxyvitamin D3 (1 alpha, [OH] D3) are widely used for treating osteodystrophy in patients with chronic renal failure. Since the pharmacokinetics of these agents during long-term oral administration are unclear, we measured the circulating concentrations of 1 alpha, 25 (OH) 2D before and after their long-term oral administration in patients receiving maintenance hemodialysis. After 12 weeks of treatment with a daily dose of 1 alpha, (OH) D3 (0.5 micrograms), the administration of a single dose (2 micrograms) of 1 alpha, (OH) D3 showed that the area under the curve over 24 h (AUC) was increased significantly compared with day 1 of therapy. In contrast, after the treatment with a daily dose of 1 alpha, 25 (OH) 2D3 (0.25 micrograms), a single dose of 1 alpha, 25 (OH) 2D3 (1 microgram) did not exhibit this effect on the AUC. A single dose of each agent produced no significant change in either the peak increment above basal values or the elimination half-time (T 1/2) of circulating plasma 1 alpha, 25 (OH) 2D. The overall basal concentration of 1 alpha, 25 (OH) 2D achieved by 1 alpha, (OH) D3 after 12 weeks of administration was cumulative, but this effect was not observed in patients on 1 alpha, 25 (OH) 2D3. These data indicate that the pharmacokinetics of the two forms of active vitamin D3 did not differ as to peak increment and T1/2 except for the AUC, even after long-term dosage.(ABSTRACT TRUNCATED AT 250 WORDS)
维生素D3的两种活性形式,即1α,25 - 二羟基维生素D3(1α,25[OH]2D3)和1α - 羟基维生素D3(1α,[OH]D3),被广泛用于治疗慢性肾衰竭患者的骨营养不良。由于这些药物长期口服给药期间的药代动力学尚不清楚,我们在接受维持性血液透析的患者中长期口服给药前后测量了1α,25(OH)2D的循环浓度。在用每日剂量的1α,(OH)D3(0.5微克)治疗12周后,单次给予1α,(OH)D3(2微克)显示,与治疗第1天相比,24小时曲线下面积(AUC)显著增加。相比之下,在用每日剂量的1α,25(OH)2D3(0.25微克)治疗后,单次给予1α,25(OH)2D3(1微克)对AUC未表现出这种作用。每种药物单次给药后,循环血浆1α,25(OH)2D的基础值以上的峰值增量或消除半衰期(T 1/2)均无显著变化。1α,(OH)D3给药12周后达到的1α,25(OH)2D的总体基础浓度是累积性的,但在使用1α,25(OH)2D3的患者中未观察到这种效应。这些数据表明,即使长期给药后,两种活性维生素D3形式的药代动力学在峰值增量和T1/2方面除AUC外并无差异。(摘要截短于250字)