Russell J E, Avioli L V
J Clin Invest. 1975 Oct;56(4):792-8. doi: 10.1172/JCI108157.
In vitro evidence presently favors a direct osteolytic effect of biologically active vitamin D metabolites. Studies were designed to evaluate the effect of 25-hydroxycholecalciferol (25OHD3) on bone collagen and mineral maturation in vivo and its dependence on parathyroid hormone (PTH). After treatment of sham-operated control and parathyroidectomized (PTX) mature rats with either 25OHD3 or an oil vehicle for 2 wk, tibial bone mineral-collagen maturation was quantitated by bromoform-toluene density gradient fractionation techniques. Intestinal calcium absorption was measured by in vivo 45Ca transport procedures. In contrast to the control group, the response to 25OHD3 of PTX rats was dramatic. Bone mineral and matrix maturation were both accelerated by 25OHD3 treatment without concomitant reduction in total bone mineral or collagen content or changes in the intestinal calcium absorption. These observations support the premise that biologically active vitamin D metabolites stimulate bone tissue maturation, and that PTH is not required in this regard.
目前的体外证据支持生物活性维生素D代谢产物具有直接溶骨作用。本研究旨在评估25-羟胆钙化醇(25OHD3)对体内骨胶原和矿物质成熟的影响及其对甲状旁腺激素(PTH)的依赖性。用25OHD3或油赋形剂对假手术对照和甲状旁腺切除(PTX)的成年大鼠进行处理2周后,采用溴仿-甲苯密度梯度分级技术对胫骨骨矿物质-胶原成熟度进行定量分析。通过体内45Ca转运程序测量肠道钙吸收。与对照组相比,PTX大鼠对25OHD3的反应显著。25OHD3处理可加速骨矿物质和基质成熟,而总骨矿物质或胶原含量没有相应减少,肠道钙吸收也没有变化。这些观察结果支持以下前提:生物活性维生素D代谢产物刺激骨组织成熟,且在这方面不需要PTH。