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大鼠骨痂区域双膦酸盐(因卡膦酸)的浓度及其对骨折愈合的影响。

Concentration of bisphosphonate (incadronate) in callus area and its effects on fracture healing in rats.

作者信息

Li J, Mori S, Kaji Y, Kawanishi J, Akiyama T, Norimatsu H

机构信息

Department of Orthopedic Surgery, Kagawa Medical University, Kita-gun, Japan.

出版信息

J Bone Miner Res. 2000 Oct;15(10):2042-51. doi: 10.1359/jbmr.2000.15.10.2042.

Abstract

The aim of the present study was to investigate effects of incadronate on early stages of fracture healing and to detect its concentration in callus area (Ca.Ar). Rats were injected three times per week with either two doses of incadronate (10 microg/kg and 100 microg/kg) or vehicle for 2 weeks. Femora were then fractured and fixed and animals were divided into pretreatment (P-10 and P-100) and continuous treatment (C-10 and C-100) groups. Incadronate treatment was stopped in P-10 and P-100 groups but continued in C-10 and C-100 groups. Animals were killed at 2 weeks and 4 weeks after fracture. Results showed significantly large callus, compared with the control, only in C-100 group at 4 weeks but not at 2 weeks. Both linear labeled surface (LS) and eroded surface (ES) decreased significantly in C-10 and C-100 groups at 2 weeks and 4 weeks. Osteoclast number (N.Oc) decreased significantly in C-10 and C-100 groups at 2 weeks but increased slightly at 4 weeks. However, there was no significant difference in the above parameters in P-10 and P-100 groups at 4 weeks. Apoptotic osteoclasts were observed only in the C-100 group at 4 weeks. A time-course decrease in incadronate concentration was detected in P-10 and P-100 groups whereas an increase was observed in C-10 and C-100 groups. These findings suggest that larger callus under incadronate treatment may result from the inhibition of bone resorption, histological characteristics of callus may be correlated with incadronate concentration, and metabolism of incadronate in bone may be related to the rate of bone turnover.

摘要

本研究的目的是探讨因卡膦酸盐对骨折愈合早期阶段的影响,并检测其在骨痂区域(Ca.Ar)的浓度。每周给大鼠注射三次两种剂量的因卡膦酸盐(10微克/千克和100微克/千克)或赋形剂,持续2周。然后将股骨骨折并固定,动物被分为预处理组(P - 10和P - 100)和持续治疗组(C - 10和C - 100)。P - 10和P - 100组停止因卡膦酸盐治疗,而C - 10和C - 100组继续治疗。在骨折后2周和4周处死动物。结果显示,与对照组相比,仅在4周时的C - 100组有明显更大的骨痂,而在2周时没有。在2周和4周时,C - 10和C - 100组的线性标记表面(LS)和侵蚀表面(ES)均显著降低。在2周时,C - 10和C - 100组的破骨细胞数量(N.Oc)显著减少,但在4周时略有增加。然而,在4周时,P - 10和P - 100组的上述参数没有显著差异。仅在4周时的C - 100组观察到凋亡破骨细胞。在P - 10和P - 100组中检测到因卡膦酸盐浓度随时间下降,而在C - 10和C - 100组中观察到浓度增加。这些发现表明,因卡膦酸盐治疗下更大的骨痂可能是由于骨吸收的抑制,骨痂的组织学特征可能与因卡膦酸盐浓度相关,并且因卡膦酸盐在骨中的代谢可能与骨转换率有关。

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