Nolte P A, Klein-Nulend J, Albers G H, Marti R K, Semeins C M, Goei S W, Burger E H
Department of Orthopaedics, Academic Medical Center, University of Amsterdam, Netherlands.
J Orthop Res. 2001 Mar;19(2):301-7. doi: 10.1016/S0736-0266(00)00027-9.
Animal and clinical studies have shown an acceleration of bone healing by the application of low-intensity ultrasound. The objective of this study was to examine in vitro the influence of low-intensity ultrasound on endochondral ossification of 17-day-old fetal mouse metatarsal rudiments. Forty-six triplets of paired metatarsal rudiments were resected 'en block' and cultured for 7 days with and without low-intensity ultrasound stimulation (30 mw/cm2). At days 1, 3, 5, and 7, the total length of the metatarsal rudiments, as well as the length of the calcified diaphysis were measured. Histology of the tissue was performed to examine its vitality. The increase in length of the calcified diaphysis during 7 days of culture was significantly higher in the ultrasound-treated rudiments compared to the untreated controls (P = 0.006). The growth of the control diaphysis was 180 +/- 30 microm (mean +/- SEM), while the growth of the ultrasound-treated diaphysis was 530 +/- 120 microm. The total length of the metatarsal rudiments was not affected by ultrasound treatment. Histology revealed a healthy condition of both ultrasound-treated and control rudiments. In conclusion, low-intensity ultrasound treatment stimulated endochondral ossification of fetal mouse metatarsal rudiments. This might be due to stimulation of activity and/or differentiation of osteoblasts and hypertrophic chondrocytes. Our results support the hypothesis that low-intensity ultrasound activates ossification via a direct effect on osteoblasts and ossifying cartilage.
动物和临床研究表明,应用低强度超声可加速骨愈合。本研究的目的是在体外检测低强度超声对17日龄胎鼠跖骨原基软骨内成骨的影响。将46对三联体的配对跖骨原基“整块”切除,在有和没有低强度超声刺激(30 mw/cm2)的情况下培养7天。在第1、3、5和7天,测量跖骨原基的总长度以及钙化骨干的长度。对组织进行组织学检查以检测其活力。与未处理的对照组相比,超声处理的原基在培养7天期间钙化骨干长度的增加明显更高(P = 0.006)。对照骨干的生长为180±30微米(平均值±标准误),而超声处理的骨干的生长为530±120微米。跖骨原基的总长度不受超声处理的影响。组织学显示超声处理和对照原基均处于健康状态。总之,低强度超声处理刺激了胎鼠跖骨原基的软骨内成骨。这可能是由于刺激了成骨细胞和肥大软骨细胞的活性和/或分化。我们的结果支持这样的假设,即低强度超声通过对成骨细胞和正在骨化的软骨的直接作用来激活骨化。