Takahashi N, Miyaura C, Horiuchi N, Suda T
J Nutr Sci Vitaminol (Tokyo). 1981;27(5):429-37. doi: 10.3177/jnsv.27.429.
The time course of change in plasma calcium levels and renal metabolism of 25-hydroxyvitamin D3 [25(OH)D3] was investigated in chicks maintained on a vitamin D-deficient diet for 4 weeks. Plasma calcium concentrations dropped sharply between the 7th and 14th day of the feeding period. Renal 25(OH)D3-1 alpha-hydroxylase activity was reciprocally enhanced concurrently with the decrease in plasma calcium levels. The elevated activity of 1 alpha-hydroxylase had declined significantly by the 21st and 28th days in spite of the more severe hypocalcemia. When graded amounts of vitamin D3 were administered to the chicks maintained on this diet for 14 or 28 days, there were considerable differences in the change of plasma calcium levels and 25(OH)D3 metabolism induced by vitamin D3 administration between the 14-day and 28-day birds. The minimal dose levels of vitamin D3 to completely suppress renal 1 alpha-hydroxylase activity were 25 micrograms in the 14-day, and 2.5 mg in the 28-day birds. These differences were not observed between the 14-day and 28-day birds when 1 alpha-hydroxyvitamin D3 [1 alpha(OH)D3] was administered. Renal adenylate cyclase activity induced by parathyroid hormone (PTH) was much lower in the 28-day chicks than that in 1-day-old and the 14-day birds. These results are explained by the hypersecretion of PTH and the subsequent refractoriness of the target organs in severe vitamin D deficiency. Plasma calcium levels per se did not appear to be a major factor in the regulation of 25(OH)D3 metabolism.
对以维生素D缺乏饮食饲养4周的雏鸡,研究了血浆钙水平变化的时间进程以及25-羟基维生素D3 [25(OH)D3]的肾脏代谢情况。在喂食期的第7天至第14天之间,血浆钙浓度急剧下降。肾脏25(OH)D3-1α-羟化酶活性在血浆钙水平下降的同时相应增强。尽管低钙血症更为严重,但到第21天和第28天时,1α-羟化酶升高的活性已显著下降。当给以这种饮食饲养14天或28天的雏鸡给予不同剂量的维生素D3时,14日龄和28日龄雏鸡在维生素D3给药后血浆钙水平变化和25(OH)D3代谢方面存在相当大的差异。完全抑制肾脏1α-羟化酶活性的维生素D3最小剂量水平在14日龄雏鸡中为25微克,在28日龄雏鸡中为2.5毫克。当给予1α-羟基维生素D3 [1α(OH)D3]时,14日龄和28日龄雏鸡之间未观察到这些差异。甲状旁腺激素(PTH)诱导的肾脏腺苷酸环化酶活性在28日龄雏鸡中比1日龄和14日龄雏鸡低得多。这些结果可以通过严重维生素D缺乏时PTH的过度分泌以及随后靶器官的不应性来解释。血浆钙水平本身似乎不是25(OH)D3代谢调节的主要因素。