Delmez J A, Tindira C, Grooms P, Dusso A, Windus D W, Slatopolsky E
Renal Division, Washington University School of Medicine, St. Louis, Missouri 63110.
J Clin Invest. 1989 Apr;83(4):1349-55. doi: 10.1172/JCI114022.
Numerous in vitro studies in experimental animals have demonstrated a direct suppressive effect of 1,25-dihydroxyvitamin D (1,25(OH)2D) on parathyroid hormone (PTH) synthesis. We therefore sought to determine whether such an effect could be demonstrated in uremic patients undergoing maneuvers designed to avoid changes in serum calcium concentrations. In addition, the response of the parathyroid gland in patients undergoing hypercalcemic suppression (protocol I) and hypocalcemic stimulation (protocol II) before and after 2 wk of intravenous 1,25(OH)2D was evaluated. In those enlisted in protocol I, PTH values fell from 375 +/- 66 to 294 +/- 50 pg (P less than 0.01) after 1,25(OH)2D administration. During hypercalcemic suppression, the "set point" (PTH max + PTH min/2) for PTH suppression by calcium fell from 5.24 +/- 0.14 to 5.06 +/- 0.15 mg/dl (P less than 0.05) with 1,25(OH)2D. A similar decline in PTH levels after giving intravenous 1,25(OH)2D was noted in protocol II patients. During hypocalcemic stimulation, the parathyroid response was attenuated by 1,25(OH)2D. We conclude that intravenous 1,25(OH)2D directly suppresses PTH secretion in uremic patients. This suppression, in part, appears to be due to increased sensitivity of the gland to ambient calcium levels.
众多针对实验动物的体外研究已证实,1,25 - 二羟维生素D(1,25(OH)₂D)对甲状旁腺激素(PTH)合成具有直接抑制作用。因此,我们试图确定在进行旨在避免血清钙浓度变化的操作的尿毒症患者中,是否能证实这种作用。此外,还评估了静脉注射1,25(OH)₂D 2周前后,接受高钙抑制(方案I)和低钙刺激(方案II)患者的甲状旁腺反应。在方案I的受试者中,给予1,25(OH)₂D后,PTH值从375±66降至294±50 pg(P<0.01)。在高钙抑制期间,钙抑制PTH的“设定点”(PTH最大值 + PTH最小值/2)在给予1,25(OH)₂D后从5.24±0.14降至5.06±0.15 mg/dl(P<0.05)。在方案II的患者中,静脉注射1,25(OH)₂D后也观察到PTH水平有类似下降。在低钙刺激期间,1,25(OH)₂D减弱了甲状旁腺反应。我们得出结论,静脉注射1,25(OH)₂D可直接抑制尿毒症患者的PTH分泌。这种抑制作用部分似乎是由于腺体对周围钙水平的敏感性增加所致。