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维生素K循环拮抗剂对骨折愈合的影响。

Effects on fracture healing of an antagonist of the vitamin K cycle.

作者信息

Dodds R A, Catterall A, Bitensky L, Chayen J

出版信息

Calcif Tissue Int. 1984 Mar;36(2):233-8. doi: 10.1007/BF02405322.

Abstract

The anticoagulant, dicumarol, inhibits the vitamin K cycle by blocking the conversion of the vitamin K epoxide. The effects of dicumarol on ossification have been tested by feeding it to rats in which a closed fracture of the metatarsals had been induced; the effects were studied up to 12 days postfracture. At 12 days, treatment with dicumarol caused a highly significant decrease in the amount of bone produced, without affecting the total size of the callus. Quantitative cytochemistry of unfixed, undemineralized sections showed that dicumarol also markedly affected the periosteal activities of glucose 6-phosphate dehydrogenase and of alkaline phosphatase in the first 2 mm from the fracture measured at 3 and 5 days postfracture when normally, new bone is first formed. In contrast, dicumarol had little effect on these activities in the fully formed callus.

摘要

抗凝血剂双香豆素通过阻断维生素K环氧化物的转化来抑制维生素K循环。双香豆素对骨化的影响已通过将其喂给已诱导跖骨闭合性骨折的大鼠进行了测试;在骨折后长达12天的时间里对其影响进行了研究。在第12天,双香豆素治疗导致所产生的骨量显著减少,而不影响骨痂的总体大小。对未固定、未脱钙切片的定量细胞化学分析表明,双香豆素在骨折后3天和5天测量时,也显著影响了距骨折处最初2毫米范围内骨膜的葡萄糖6-磷酸脱氢酶和碱性磷酸酶活性,而正常情况下新骨在此阶段开始形成。相比之下,双香豆素对完全形成的骨痂中的这些活性几乎没有影响。

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