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慢性肾衰竭中骨化三醇的肾外生成

Extra-renal production of calcitriol in chronic renal failure.

作者信息

Dusso A, Lopez-Hilker S, Rapp N, Slatopolsky E

机构信息

Department of Medicine, Washington University School of Medicine, St. Louis, Missouri.

出版信息

Kidney Int. 1988 Sep;34(3):368-75. doi: 10.1038/ki.1988.190.

DOI:10.1038/ki.1988.190
PMID:3172645
Abstract

Renal 1-alpha-hydroxylase activity is tightly regulated in normal humans and intact animals. No significant changes in serum 1,25(OH)2D levels occur in response to vitamin D challenge. However, conflicting reports have appeared in the literature with regard to stimulation of 1,25(OH)2D production after 25(OH)D administration in uremia. To provide further insight into this issue, 25(OH)D at a dose of 100 micrograms every other day for two weeks followed by 50 micrograms every other day for the next two weeks was given orally to seven uremic mongrel dogs. After two weeks of 25(OH)D therapy, 1,25(OH)2D levels increased from 16.4 +/- 0.9 to 28.0 +/- 1.9 pg/ml (P less than 0.001) in parallel with a fourfold increase in 25(OH)D concentrations from a basal of 50.1 +/- 6.5 to 203.2 +/- 18.1 ng/ml. No significant changes in serum i-PTH, ICa or P were observed. Linear regression analysis of the relationship between serum concentrations of 1,25(OH)2D versus 25(OH)D, for each dog during this period, showed highly significant correlation coefficients. To evaluate the possibility that extra-renal sites contribute to the described enhanced 1,25(OH)2D net synthesis after 25(OH)D treatment, similar studies were performed in four anephric patients undergoing hemodialysis. Basal serum 1,25(OH)2D levels were 5.5 +/- 2.4 pg/ml and increased to 19.6 +/- 5.0 pg/ml after 25(OH)D administration. A significant correlation was also found for the relationship between serum levels of 1,25(OH)2D and 25(OH)D in anephrics (r = 0.72, P less than 0.001). The same therapy in four normal volunteers showed no significant changes in serum 1,25(OH)2D concentrations.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在正常人和完整动物中,肾1-α-羟化酶活性受到严格调控。维生素D激发试验后,血清1,25(OH)₂D水平无显著变化。然而,关于尿毒症患者给予25(OH)D后刺激1,25(OH)₂D生成的研究,文献报道存在矛盾。为进一步深入了解该问题,对7只尿毒症杂种犬口服25(OH)D,剂量为每2天100微克,持续2周,随后每2天50微克,再持续2周。25(OH)D治疗2周后,1,25(OH)₂D水平从16.4±0.9 pg/ml升至28.0±1.9 pg/ml(P<0.001),同时25(OH)D浓度从基础值50.1±6.5 ng/ml增至203.2±18.1 ng/ml,升高了4倍。血清i-PTH、总钙或磷无显著变化。在此期间,对每只犬血清1,25(OH)₂D与25(OH)D浓度关系进行线性回归分析,显示相关系数高度显著。为评估肾外部位对25(OH)D治疗后所述1,25(OH)₂D净合成增加的贡献,对4例接受血液透析的无肾患者进行了类似研究。基础血清1,25(OH)₂D水平为5.5±2.4 pg/ml,给予25(OH)D后升至19.6±5.0 pg/ml。无肾患者血清1,25(OH)₂D与25(OH)D水平之间的关系也存在显著相关性(r = 0.72,P<0.001)。4名正常志愿者接受相同治疗后,血清1,25(OH)₂D浓度无显著变化。(摘要截选至250字)

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