Prince R L, Wark J D, Eisman J A, Danks J A, Larkins R G
Horm Metab Res. 1983 Aug;15(8):399-403. doi: 10.1055/s-2007-1018734.
The conversion of 25-hydroxyvitamin D3 (25 OH D3) to 1,25-dihydroxyvitamin D3 (1,25-(OH)2D3), 24,25-dihydroxyvitamin D3 (24,25-(OH)2D3) and 1,24,25-trihydroxyvitamin D3 (1.24,25-(OH)3D3) was studied in renal tubules prepared from chicks raised on a vitamin D deficient diet with or without vitamin D supplementation. As described previously, in tubules from vitamin D deficient chicks, cyclic AMP caused an increase in the net accumulation of 1,25-(OH)2D3, the major metabolite formed under these circumstances. This stimulation was shown to be due to an increased maximum velocity of the hydroxylation reaction. There was also a significant inhibition of the net accumulation of 24,25-(OH)2D3. Cyclic GMP caused a significant inhibition of 1,25-(OH)2D3 formation and stimulation of the net accumulation of 24,25-(OH)2D3. In chicks supplemented with high doses of vitamin D, 24,25-(OH)2D3 was the major metabolite of 25 OH D3 detected and 1-hydroxylase activity was negligible. Under these circumstances, neither cyclic AMP nor cyclic GMP affected net accumulation of 24,25(OH)2D3. This suggested that the apparent effect of the nucleotides on formation of 24,25-(OH)2D3 may have been due to further metabolism of 24,25-(OH)2D3 when 1-hydroxylase activity was high. It is concluded that cyclic AMp and cyclic GMP have reciprocal effects on renal 25 OH D3-1-hydroxylase activity, and both should be considered potential intracellular regulators of 25 OH D3 metabolism.
在以维生素D缺乏饮食饲养且补充或未补充维生素D的雏鸡制备的肾小管中,研究了25-羟基维生素D3(25 OH D3)向1,25-二羟基维生素D3(1,25-(OH)2D3)、24,25-二羟基维生素D3(24,25-(OH)2D3)和1,24,25-三羟基维生素D3(1,24,25-(OH)3D3)的转化。如先前所述,在维生素D缺乏雏鸡的肾小管中,环磷酸腺苷(cAMP)导致1,25-(OH)2D3的净积累增加,1,25-(OH)2D3是在这些情况下形成的主要代谢产物。这种刺激被证明是由于羟化反应的最大速度增加。24,25-(OH)2D3的净积累也受到显著抑制。环磷酸鸟苷(cGMP)导致1,25-(OH)2D3形成的显著抑制,并刺激24,25-(OH)2D3的净积累。在补充高剂量维生素D的雏鸡中,24,25-(OH)2D3是检测到的25 OH D3的主要代谢产物,1-羟化酶活性可忽略不计。在这些情况下,cAMP和cGMP均不影响24,25-(OH)2D3的净积累。这表明,当1-羟化酶活性较高时,核苷酸对24,25-(OH)2D3形成的明显影响可能是由于24,25-(OH)2D3的进一步代谢。结论是,cAMP和cGMP对肾脏25 OH D3-1-羟化酶活性具有相互作用,两者均应被视为25 OH D3代谢的潜在细胞内调节因子。