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维生素D代谢产物对绝经后骨质疏松大鼠模型骨代谢的影响。

Effect of vitamin D metabolites on bone metabolism in a rat model of postmenopausal osteoporosis.

作者信息

Matsumoto T, Ezawa I, Morita K, Kawanobe Y, Ogata E

出版信息

J Nutr Sci Vitaminol (Tokyo). 1985 Dec;31 Suppl:S61-5. doi: 10.3177/jnsv.31.supplement_s61.

Abstract

A rat model of postmenopausal osteoporosis was introduced, using ovariectomized rats on a low Ca diet. CT treatment of these animals for one month prevented the decrease in both mineral contents and physical properties of the femoral bone. Treatment of the animals with 1,25(OH)2D3 was effective in increasing bone mineral contents and maintaining positive mineral balance, but did not increase the physical tolerance of bones. In contrast, 24,25(OH)2D3 increased the breaking force of the femoral bone, with minimal effect on bone mineral contents and mineral balance. These results suggest that 1,25(OH)2D3 and 24,25(OH)2D3 act differently on the matrix phase and mineral phase of bones, but that they act together to maintain mineral balance and structural integrity of bones. The mechanism of how these vitamin D metabolites affect bone metabolism remain to be clarified.

摘要

采用低钙饮食的去卵巢大鼠建立绝经后骨质疏松症大鼠模型。对这些动物进行为期一个月的CT治疗可防止股骨矿物质含量和物理特性的下降。用1,25(OH)2D3治疗动物可有效增加骨矿物质含量并维持正矿物质平衡,但不会增加骨骼的物理耐受性。相比之下,24,25(OH)2D3增加了股骨的断裂力,对骨矿物质含量和矿物质平衡的影响最小。这些结果表明,1,25(OH)2D3和24,25(OH)2D3对骨骼的基质相和矿物质相的作用不同,但它们共同作用以维持骨骼的矿物质平衡和结构完整性。这些维生素D代谢物如何影响骨代谢的机制仍有待阐明。

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