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大鼠骨骼疾病中骨钙素的骨浓度和血清浓度与循环中1,25 - 二羟维生素D3水平的关系

Bone and serum concentrations of osteocalcin as a function of 1,25-dihydroxyvitamin D3 circulating levels in bone disorders in rats.

作者信息

Lian J B, Carnes D L, Glimcher M J

出版信息

Endocrinology. 1987 May;120(5):2123-30. doi: 10.1210/endo-120-5-2123.

Abstract

Osteocalcin, the vitamin K-dependent protein in bone containing gamma-carboxyglutamic acid, has been found to be significantly decreased in the osteomalacic bone of chicks made vitamin D deficient for 6 weeks. To evaluate whether this decrease in bone osteocalcin was due directly to the decrease or absence of vitamin D and its metabolites or to the secondary hypocalcemia and osteomalacia or other changes accompanying the deficiency of vitamin D, three experimental groups of Holtzman rats were studied. One group was made rachitic by a diet deficient in vitamin D, and the other groups were made rachitic by diets deficient in inorganic orthophosphate or calcium. The changes in bone and serum osteocalcin, serum 1,25-dihydroxyvitamin D3 [1,25-(OH)2D3], and bone mineral content were evaluated, and morphological evaluation of bone was made. In the vitamin D-deficient animals, osteomalacia was evident histologically by 7 weeks, at which time serum 1,25-(OH)2D3 was not detectable, bone osteocalcin was decreased by 50%, and serum osteocalcin was decreased by 20%. In the animals fed a diet deficient in either calcium or inorganic orthophosphate but which were not depleted of vitamin D, the osteocalcin content of osteomalcic bone was normal, and an increase in the concentration of serum osteocalcin accompanied an increase in serum 1,25-(OH)2D3. These data are consistent with the conclusion that the metabolism of osteocalcin is affected by serum 1,25-(OH)2D3 and that the diminished level of osteocalcin in the bone of vitamin D-deficient animals is the result of a direct action of the metabolites and is not secondary to a decrease in the mineralization of bone tissue.

摘要

骨钙素是骨骼中一种依赖维生素K且含有γ-羧基谷氨酸的蛋白质,研究发现,在维生素D缺乏6周的雏鸡的骨软化骨中,骨钙素显著减少。为了评估骨钙素的这种减少是直接由于维生素D及其代谢产物的减少或缺乏,还是由于继发性低钙血症和骨软化症,抑或是维生素D缺乏伴随的其他变化,研究了三组实验性的霍尔茨曼大鼠。一组通过缺乏维生素D的饮食导致患佝偻病,其他组通过缺乏无机正磷酸盐或钙的饮食导致患佝偻病。评估了骨骼和血清骨钙素、血清1,25-二羟基维生素D3 [1,25-(OH)2D3]以及骨矿物质含量的变化,并对骨骼进行了形态学评估。在维生素D缺乏的动物中,7周时组织学上明显出现骨软化症,此时血清1,25-(OH)2D3检测不到,骨钙素减少50%,血清骨钙素减少20%。在喂食缺乏钙或无机正磷酸盐但未缺乏维生素D的饮食的动物中,骨软化骨的骨钙素含量正常,血清骨钙素浓度的增加伴随着血清1,25-(OH)2D3浓度的增加。这些数据与以下结论一致,即骨钙素的代谢受血清1,25-(OH)2D3的影响,维生素D缺乏动物骨骼中骨钙素水平的降低是代谢产物直接作用的结果,而非继发于骨组织矿化的减少。

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