大鼠肾单位分级质量减少和1,25-二羟基维生素D3的肾脏合成。

Y Kawaguchi, Y Kimura, M Yamamoto, N Imamura, I Tukui, N Horiuchi, T Suda, Y Ogura, Y Oda, T Miyahara
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引用次数: 0

摘要

研究了部分切除肾元分级减重对维生素D缺乏大鼠的影响,以及甲状旁腺激素和膳食磷对1,25-二羟基维生素D [1,25(OH)2D]生成的影响。在部分肾切除术后48小时(急性实验)或2周(慢性实验),测定体内[3H]25羟基维生素D (25- ohd)产生[3H]1,25(OH)2D的速率。1,25(OH)2D的产生与剩余的肾元质量成比例地减少,在任何水平的肾元质量减少的情况下,慢性实验并不比急性实验更大。相比之下,6只肾切除大鼠中的5只在急性实验中血浆肌酐升高,而在慢性实验中没有升高,这表明肾脏排泄功能的代偿机制而不是1,25(OH)2D的产生。此外,在任何水平的肾元质量减少下,低磷饲料的大鼠这种活性代谢物的产生并不比正常或高磷饲料的大鼠多。在喂食正常或高磷饮食的大鼠,在服用[3H]-25)OHD前12小时进行甲状旁腺切除术可抑制任意水平的肾单位质量减少的1,25(OH)2D生成。这些数据表明,在实验性急性和慢性肾功能衰竭中,1,25(OH)2D的产生与残余肾元质量成比例,甲状旁腺激素可能会增强肾功能衰竭中25OHD的代谢,也可能是正常或高磷饮食中1,25(OH)2D的关键。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Graded nephron mass reduction and renal synthesis of 1,25-dihydroxyvitamin D3 in the rat.

The effect of graded nephron mass reduction by partial nephrectomy and the influence of parathyroid hormone and dietary phosphorus (P) on the production of 1,25-dihydroxy-vitamin D [1,25(OH)2D] were studied in vitamin D deficient rats. At 48 hours (acute experiments) or 2 weeks (chronic experiment) after partial nephrectomy, the rates of [3H]1,25(OH)2D production from [3H]25 hydroxyvitamin D (25-OHD) were measured in vivo. The production of 1,25(OH)2D decreased in proportion to the remaining nephron mass, and it was not greater in chronic experiments than in acute experiments at any level of nephron mass reduction. By contrast, plasma creatinine was elevated in 5 of 6 nephrectomized rats in acute, but not in chronic, experiments, suggesting the compensatory mechanism for renal excretory function but not for 1,25(OH)2D production. Further, at any level of nephron mass reduction, the production of this active metabolite was not greater in rats fed low P diet than those fed normal or high P diets. Thyroparathyroidectomy at 12 hours prior to a dose of [3H]-25)OHD suppressed 1,25(OH)2D production at any level of nephron mass reduction in rats fed normal or high P diet. These data suggest that in both experimental acute and chronic renal failure 1,25(OH)2D production is proportional to residual nephron mass and that parathyroid hormone may enhance the metabolism of 25OHD in renal failure and also may be critical for 1,25(OH)2D in normal or high P diet.

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