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肾衰竭中影响骨化三醇代谢的因素。

Factors influencing calcitriol metabolism in renal failure.

作者信息

Hsu C H, Patel S

机构信息

Department of Internal Medicine, University of Michigan Medical School, Ann Arbor.

出版信息

Kidney Int. 1990 Jan;37(1):44-50. doi: 10.1038/ki.1990.6.

Abstract

Metabolic clearance rate (MCR) and production rate (PR) of calcitriol is decreased in experimental renal failure. In this experiment, we studied uremia and secondary hyperparathyroidism as possible causes of the abnormal calcitriol metabolism. Normal rats were made uremic by infusing phosphorus-free urine for 24 hours. Both the MCR (0.22 +/- 0.01 ml/min/kg, N = 6 P less than 0.001) and the PR (16.6 +/- 1.97 ng/kg/day, P less than 0.01) of calcitriol were significantly suppressed in normal rats following urine infusion when compared to saline infused rats (MCR, 0.30 +/- 0.01; PR, 32.9 +/- 4.1, N = 6). Different levels of protein intake by rats with renal failure produced by subtotal nephrectomy also alter the PR but not the MCR of calcitriol. Thus, the synthesis of calcitriol was significantly lower in rats with renal failure fed a high protein (50% protein) diet (17.6 +/- 0.7 ng/kg/day, N = 8, P less than 0.001) than in rats with renal failure fed a normal protein (20% protein) diet (22.2 +/- 1.4, N = 7). Thyroparathyroidectomy (TPTX) did not alter the MCR of calcitriol in renal failure, even though parathyroid hormone, which may suppress the degradation enzyme, could be elevated in this model of renal failure. The MCR of TPTXed rats with renal failure (0.15 +/- 0.01 ml/min/kg, N = 7) remained lower than that of the TPTXed control rats (0.19 +/- 0.01, N = 7, P less than 0.001), and chronic infusion of PTH to TPTXed rats with renal failure did not change the MCR of calcitriol (0.15 +/- 0.01, vs. control, 0.24 +/- 0.01).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

实验性肾衰竭时,骨化三醇的代谢清除率(MCR)和生成率(PR)降低。在本实验中,我们研究了尿毒症和继发性甲状旁腺功能亢进作为骨化三醇代谢异常的可能原因。通过输注无磷尿液24小时使正常大鼠患尿毒症。与输注生理盐水的大鼠(MCR,0.30±0.01;PR,32.9±4.1,N = 6)相比,输注尿液后的正常大鼠骨化三醇的MCR(0.22±0.01 ml/min/kg,N = 6,P<0.001)和PR(16.6±1.97 ng/kg/天,P<0.01)均显著降低。通过肾大部切除造成肾衰竭的大鼠不同水平的蛋白质摄入也会改变骨化三醇的PR,但不会改变其MCR。因此,喂食高蛋白(50%蛋白质)饮食的肾衰竭大鼠(17.6±0.7 ng/kg/天,N = 8,P<0.001)骨化三醇的合成显著低于喂食正常蛋白质(20%蛋白质)饮食的肾衰竭大鼠(22.2±1.4,N = 7)。甲状腺甲状旁腺切除术(TPTX)并未改变肾衰竭大鼠骨化三醇的MCR,尽管在这种肾衰竭模型中可能抑制降解酶的甲状旁腺激素会升高。TPTX的肾衰竭大鼠的MCR(0.15±0.01 ml/min/kg,N = 7)仍低于TPTX的对照大鼠(0.19±0.01,N = 7,P<0.001),并且向TPTX的肾衰竭大鼠长期输注甲状旁腺激素并未改变骨化三醇的MCR(0.15±0.01,对照为0.24±0.01)。(摘要截断于250字)

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