Pirttiniemi Pertti, Kantomaa Tuomo, Sorsa Timo
Department of Orthodontics and Oral Development, Institutes of Dentistry, University of Oulu, Finland.
Eur J Orthod. 2004 Feb;26(1):1-5. doi: 10.1093/ejo/26.1.1.
The aim of this study was to measure the effect of decreased temporomandibular loading on the proliferative activity and the level of matrix production of the condylar cartilage. The effect of reduced joint loading on the activity of stromelysin-1 (MMP-3), which has been associated with conditions of articular cartilage matrix breakdown, was also examined. Eighty 14-day-old female rats were assigned to two groups. Following weaning at 20 days, the experimental group was fed a soft diet and the incisors were shortened regularly to keep them out of occlusion. The controls were fed a hard diet. The activity of tritiated thymidine incorporation and the incorporation of radiolabelled sulphur were measured 2, 6, 12, 24 and 48 hours after initiation of the experiment. The radiolabelled sulphur intake was significantly lower in the condylar cartilage of the experimental group 6-24 hours after initiation of the experiment, and tritiated thymidine activity was lower after 12-24 hours, indicating lower proliferation and matrix production. The cartilage in the experimental group showed marked immunostaining against MMP-3 in all cartilage layers 9 days after initiation of the experiment. In the control group, the staining was clearly seen only in the superficial fibrous layer and in the erosion front. A marked reduction in proliferative activity and proteoglycan synthesis in mandibular condylar cartilage was found after a continuous soft diet and suppressed incisal mastication in the rat. The results show that sufficient loading is important for condylar cartilage growth, to maintain both ideal proliferation and matrix chondrocyte production.
本研究的目的是测量颞下颌负荷降低对髁突软骨增殖活性和基质产生水平的影响。还研究了关节负荷降低对基质金属蛋白酶-1(MMP-3)活性的影响,MMP-3与关节软骨基质分解的情况有关。80只14日龄雌性大鼠被分为两组。在20日龄断奶后,实验组喂食软食,并定期缩短门齿以使其不处于咬合状态。对照组喂食硬食。在实验开始后2、6、12、24和48小时测量氚标记胸腺嘧啶核苷掺入活性和放射性标记硫的掺入情况。实验开始后6 - 24小时,实验组髁突软骨中放射性标记硫的摄入量显著降低,12 - 24小时后氚标记胸腺嘧啶核苷活性降低,表明增殖和基质产生较低。实验开始9天后,实验组软骨在所有软骨层均显示出针对MMP-3的明显免疫染色。在对照组中,仅在浅表纤维层和侵蚀前沿可见染色。在大鼠持续喂食软食并抑制切牙咀嚼后,下颌髁突软骨的增殖活性和蛋白聚糖合成明显降低。结果表明,足够的负荷对髁突软骨生长很重要,以维持理想的增殖和基质软骨细胞产生。