Wientroub S, Reddi A H
Department of Orthopaedic Surgery, Tel-Aviv Medical Centre, Israel.
Calcif Tissue Int. 1988 Apr;42(4):255-60. doi: 10.1007/BF02553752.
Samples of demineralized bone matrix (DBM) were exposed to graduated doses of radiation (1-15 Megarad) (Mrad) utilizing a linear accelerator and then implanted into the thoracic region of Long-Evans rats. Subcutaneous implantation of DBM into allogenic rats induces endochondral bone. In response to matrix implantation, a cascade of events ensues; mesenchymal cell proliferation on day 3 postimplantation, chondrogenesis on day 7, calcification of the cartilagenous matrix and chondrolysis on day 9, and osteogenesis on day 11 resulting in formation of an ossicle containing active hemopoietic tissue. Bone formation was assessed by measuring alkaline phosphatase activity, the rate of mineralization was determined by measuring 45Ca incorporation to bone mineral, and 40Ca content measured the extent of mineralization; acid phosphatase activity was used as a parameter for bone resorption. The dose of radiation (2.5 Mrad) currently used by bone banks for sterilization of bone tissue did not destroy the bone induction properties of DBM. Furthermore, radiation of 3-5 Mrad even enhanced bone induction, insofar as it produced more bone at the same interval of time than was obtained from unirradiated control samples. None of the radiation doses used in these experiments abolished bone induction, although the response induced by matrix irradiated with doses higher than 5 Mrad was delayed.
利用线性加速器将脱矿骨基质(DBM)样本暴露于不同剂量的辐射(1 - 15兆拉德)(Mrad)下,然后植入Long - Evans大鼠的胸部区域。将DBM皮下植入同种异体大鼠可诱导软骨内成骨。响应基质植入,一系列事件随之发生:植入后第3天间充质细胞增殖,第7天软骨形成,第9天软骨基质钙化和软骨溶解,第11天骨生成,导致形成含有活跃造血组织的小骨。通过测量碱性磷酸酶活性评估骨形成,通过测量45Ca掺入骨矿物质来确定矿化速率,通过测量40Ca含量来测量矿化程度;酸性磷酸酶活性用作骨吸收的参数。目前骨库用于骨组织灭菌的辐射剂量(2.5 Mrad)并未破坏DBM的骨诱导特性。此外,3 - 5 Mrad的辐射甚至增强了骨诱导,因为在相同的时间间隔内,它比未辐照的对照样本产生了更多的骨。尽管用高于5 Mrad剂量辐照的基质诱导的反应有所延迟,但这些实验中使用的任何辐射剂量均未消除骨诱导。