Ersozlu Salim, Sarisozen Bartu, Ozer Ozgur, Adim Saduman Balaban, Sahin Orcun
Faculty of Medicine, Department of Orthopaedics and Traumatology, Istinye University, Liv Hospital, İstanbul, Turkey.
Faculty of Medicine, Department of Orthopaedics and Traumatology, Uludag University, Bursa, Turkey.
J Exp Orthop. 2017 Dec;4(1):25. doi: 10.1186/s40634-017-0100-x. Epub 2017 Jul 20.
Although, glucocorticoid (GC) and calcitonin-induced changes in bone repair have been studied previously, the exact effects of these on fracture healing remain controversial. Hence, the purpose of this experimental study is to determine biochemical and histological effects of locally administrated GC and systemically administrated calcitonin on the kinetics of healing response after bone marrow ablation in rats.
After having undergone marrow ablation, a steroid-treated group of rats (n = 24) received a single dose of intramedullary methylprednisolone (2 mg/kg), a calcitonin-treated group (n = 24) received intermittently administrated subcutaneous salmon calcitonin (16 IU/kg), and a control group (n = 24) received intramedullary saline (25 μl).
Blood samples taken on days 1, 3, 7, 9, and 15 after ablation showed an increase in serum calcium, alkaline phosphatase (ALP), and phosphate levels in the Calcitonin and Control groups. Levels of calcium and ALP peaked on day 7 after ablation. However, an increase in phosphate levels indicated a biphasic reaction that peaked on the third and ninth day after ablation. Hypercalcemia was not observed in Steroid group because of the inhibition of osteoclastic bone resorption. In that group, the serum levels of ALP and phosphate were lower than baseline levels. The levels of urinary calcium excretion peaked 3 to 7 days after marrow ablation in the control group and 7 to 9 days after that procedure in the steroid group. Histologic evaluation showed that the rats in the control group demonstrated the expected healing period according to the histological grades and that a delay in healing occurred in the calcitonin group after day 9 because of the inhibition of osteoclastic bone resorption. All rats in the steroid group exhibited a decrease and delayed healing response.
Total serum calcium, phosphate, and ALP levels increased after bilateral tibial bone marrow ablation and urine calcium and hydroxyproline excretion also increased as a factor of bone resorption. Subcutaneously administrated salmon calcitonin did not affect biochemical changes after marrow ablation. Single-dose intramedullary methylprednisolone inhibited extra-tibial bone resorption induced by cytokines after bone marrow ablation.
尽管此前已对糖皮质激素(GC)和降钙素诱导的骨修复变化进行了研究,但它们对骨折愈合的确切影响仍存在争议。因此,本实验研究的目的是确定局部给予GC和全身给予降钙素对大鼠骨髓消融后愈合反应动力学的生化和组织学影响。
在进行骨髓消融后,一组接受类固醇治疗的大鼠(n = 24)接受单剂量髓内甲基强的松龙(2 mg/kg),一组接受降钙素治疗的大鼠(n = 24)间歇性皮下注射鲑鱼降钙素(16 IU/kg),对照组(n = 24)接受髓内生理盐水(25 μl)。
在消融后第1、3、7、9和15天采集的血样显示,降钙素组和对照组的血清钙、碱性磷酸酶(ALP)和磷酸盐水平升高。钙和ALP水平在消融后第7天达到峰值。然而,磷酸盐水平的升高表明出现双相反应,在消融后第3天和第9天达到峰值。由于破骨细胞骨吸收受到抑制,类固醇组未观察到高钙血症。在该组中,ALP和磷酸盐的血清水平低于基线水平。对照组尿钙排泄水平在骨髓消融后3至7天达到峰值,类固醇组在该操作后7至9天达到峰值。组织学评估显示,对照组大鼠根据组织学分级表现出预期的愈合期,但由于破骨细胞骨吸收受到抑制,降钙素组在第9天后出现愈合延迟。类固醇组的所有大鼠均表现出愈合反应降低和延迟。
双侧胫骨骨髓消融后,血清总钙、磷酸盐和ALP水平升高,尿钙和羟脯氨酸排泄也因骨吸收而增加。皮下注射鲑鱼降钙素对骨髓消融后的生化变化无影响。单剂量髓内甲基强的松龙可抑制骨髓消融后细胞因子诱导的胫骨外骨吸收。