Seo E G, Norman A W
Department of Biochemistry, University of California, Riverside, USA.
J Bone Miner Res. 1997 Apr;12(4):598-606. doi: 10.1359/jbmr.1997.12.4.598.
To investigate the possible biological actions of 24,25-dihydroxyvitamin D3 (24,25(OH)2D3), a tibial fracture-healing model was established in White Leghorn chicks. Three-week-old White Leghorn chicks fed a vitamin D3-replete diet were divided into four groups (control, anesthetized, sham, and fractured). On varying days after tibial fracture (F) or sham manipulation (S), renal 25(OH)D3-1 alpha-hydroxylase and 25(OH)D3-24-hydroxylase (24-hydroxylase) activities and serum Ca2+ concentrations were measured. Metofane anesthesia was found to have no effect on the activity of either of the hydroxylases; the activities of the hydroxylases in the control, anesthetized, and sham-operated birds were similar. By 10 days after tibial fracture, the renal 24-hydroxylase activity increased more than 3-fold in F (1.33 +/- 0.07 pmol/mg of protein) as compared with S (0.42 +/- 0.03 pmol/mg of protein) (p < 0.0001). A time-dependent study of the renal 24-hydroxylase activity during the fracture repair process revealed a slow increase from the first day after fracture, a higher activity at 8 days, which peaked at 10-11 days, which is consistent with the formation of the callus. The 24-hydroxylase activity then returned to the same level as the sham group 14 days after fracture. There was no significant difference in serum Ca2+ levels between the F and S groups over the 3-week postfracture period. Serum levels of vitamin D3 metabolites were also measured during the fracture healing process: a 3.4x increase of the 24,25(OH)2D3 level in the fractured group (3.64 +/- 1.16 nM) was observed as compared with the control groups (1.08 +/- 0.49 nM) at 10 days after fracture (p = 0.068). No significant differences were observed in the plasma levels of 25(OH)D3 or 1 alpha, 25(OH)2D3 between the group with a fracture and the controls. Exposure of primary chick kidney cells in culture to serum obtained from chicks with a tibial fracture for 20 h resulted in an approximately 40% increase in the activity of the 24-hydroxylase as compared with cells exposed to serum from control birds. These results suggest that 24,25(OH)2D3 is involved in the early process of fracture repair and that there is some form of physiological communication between the fractured bone and the kidney so as to increase the renal 24-hydroxylase and the circulating concentration of this metabolite.
为研究24,25 - 二羟基维生素D3(24,25(OH)2D3)可能的生物学作用,在白来航鸡中建立了胫骨骨折愈合模型。将三周龄、喂食富含维生素D3日粮的白来航鸡分为四组(对照组、麻醉组、假手术组和骨折组)。在胫骨骨折(F)或假手术操作(S)后的不同时间,测量肾脏25(OH)D3 - 1α - 羟化酶和25(OH)D3 - 24 - 羟化酶(24 - 羟化酶)活性以及血清Ca2+浓度。发现甲氧氟烷麻醉对两种羟化酶的活性均无影响;对照组、麻醉组和假手术组鸡的羟化酶活性相似。胫骨骨折后10天,与假手术组(0.42±0.03 pmol/mg蛋白质)相比,骨折组(F)肾脏24 - 羟化酶活性增加了3倍多(1.33±0.07 pmol/mg蛋白质)(p<0.0001)。对骨折修复过程中肾脏24 - 羟化酶活性的时间依赖性研究显示,骨折后第一天开始缓慢增加,8天时活性较高,在10 - 11天达到峰值,这与骨痂形成一致。然后,24 - 羟化酶活性在骨折后14天恢复到与假手术组相同的水平。在骨折后的3周内,骨折组和假手术组之间的血清Ca2+水平没有显著差异。在骨折愈合过程中还测量了维生素D3代谢产物的血清水平:骨折后10天,骨折组(3.64±1.16 nM)的24,25(OH)2D3水平比对照组(1.08±0.49 nM)增加了3.4倍(p = 0.068)。骨折组和对照组之间的25(OH)D3或1α,25(OH)2D3血浆水平没有显著差异。将原代鸡肾细胞在培养中暴露于胫骨骨折鸡的血清20小时,与暴露于对照鸡血清的细胞相比,24 - 羟化酶活性增加了约40%。这些结果表明,24,25(OH)2D3参与骨折修复的早期过程,并且骨折骨与肾脏之间存在某种形式的生理通讯,从而增加肾脏24 - 羟化酶和这种代谢产物的循环浓度。