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1-α-羟基胆钙化醇(1-α-OH-D3)与甲状旁腺活性介导的钙缺乏性骨质疏松症中成年雄性大鼠的形态学和生化变化的最佳钙摄入量

1-Alpha-OH-cholecalciferol (1-alpha-OH-D3) and optimal calcium intake in calcium deficiency osteoporosis mediated by parathyroid activity morphologic and biochemical changes in adult male rats.

作者信息

Lindholm T S, Nilsson O S, Lindholm T C

出版信息

Acta Vitaminol Enzymol. 1985;7(1-2):39-47.

PMID:4036758
Abstract

By feeding adult male rats a calcium deficient diet for a period of 6 weeks osteoporosis can be induced with respect to significant changes in mass, turnover, chemical composition, and morphology of bone and parathyroid glands. When subsequently treating the osteoporotic rats with a combination of 1-alpha-OH-cholecalciferol (1-alpha-OH-D3) and optimal calcium intake osteoporosis as well as morphologic changes of parathyroids can be almost totally reversed as soon as after 2 weeks and completely after 4 and 6 weeks. Notwithstanding the change to an optimal calcium intake seems to be more important in normalizing the osteoporotic skeleton resulting from calcium deficiency than is the ingestion of 1-alpha-OH-D3, which may per se induce new bone formation.

摘要

通过给成年雄性大鼠喂食6周缺钙饮食,可诱导其骨骼和甲状旁腺在质量、周转率、化学成分及形态方面发生显著变化,从而引发骨质疏松。随后,用1-α-羟基胆钙化醇(1-α-OH-D3)与最佳钙摄入量联合治疗骨质疏松大鼠,2周后骨质疏松及甲状旁腺的形态变化几乎可完全逆转,4周和6周后则可完全逆转。尽管如此,对于因缺钙导致的骨质疏松骨骼,恢复到最佳钙摄入量似乎比摄入1-α-OH-D3在使其恢复正常方面更为重要,因为1-α-OH-D3本身可能会诱导新骨形成。

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