Shedden R, Dunham J, Bitensky L, Catterall A, Chayen J
Calcif Tissue Res. 1976 Nov 24;22(1):19-25. doi: 10.1007/BF02010342.
The quantitative changes in alkaline phosphatase activity in the periosteal cells close to the fracture in rat metatarsal bones has been measured during the first 5 days postfracture. This study has been made possible by two technological advances, firstly the development of cryostat microtomy for cutting unfixed, undemineralised bone, and secondly the use of scanning and integrating microdensitometry for quantifying the activity in each periosteal cell. The results showed a loss of alkaline phosphatase activity close to the fracture site, with activity rising to normal values 0.8-1.0 mm from the site. No alkaline phosphatase activity was found in the cells which proliferated from the periosteum. It is suggested that reduced glutathione could cause such inhibition.
在大鼠跖骨骨折后的前5天,对靠近骨折部位的骨膜细胞中碱性磷酸酶活性的定量变化进行了测量。两项技术进步使这项研究成为可能,首先是用于切割未固定、未脱矿骨的低温切片技术的发展,其次是使用扫描和积分显微密度测定法来量化每个骨膜细胞中的活性。结果显示,骨折部位附近的碱性磷酸酶活性降低,距该部位0.8 - 1.0毫米处活性升至正常值。从骨膜增殖的细胞中未发现碱性磷酸酶活性。有人认为还原型谷胱甘肽可能导致这种抑制作用。