Park Jung Ho, Park Jong Hoon, Yu Hwa Young, Seok Hyun
Department of Orl and Maxillofacial Surgery, School of Dentistry, Jeonbuk National University, Jeonju 54896, Republic of Korea.
Department of Oral Pathology, School of Dentistry, Jeonbuk National University, Jeonju 54896, Republic of Korea.
Biomimetics (Basel). 2024 Aug 1;9(8):466. doi: 10.3390/biomimetics9080466.
The effects of aging on the healing capacity of maxillofacial bone defects have not been studied. The aim of this study was to evaluate the effects of aging on the regeneration of round bony defects in the mandible. We created a round-shaped bony defect in the mandibular angle area in rats of different ages (2-[2 M], 10-[10 M], and 20-month-old [20 M]) and evaluated new bone regeneration in these groups. Changes in bone turnover markers such as alkaline phosphatase, procollagen type I N-terminal propeptide (PINP), cross-linked C-telopeptide of type I collagen, and tartrate-resistant acid phosphatase 5B (TRAP5b) were investigated. The bone volume/total volume and bone mineral density of the 20 M group were significantly higher than those of the 2 M group ( = 0.029, 0.019). A low level of the bone formation marker PINP was observed in the 20 M group, and a high level of the bone resorption marker TRAP5b was observed in the 10 M and 20 M groups. Micro-computed tomography (µ-CT) results showed that older rats had significantly higher bone formation than younger rats, with lower serum levels of PINP and higher levels of TRAP5b. The local environment of the old rat bone defects, surrounded by thickened bone, may have affected the results of our study. In conclusion, old rats showed greater new bone regeneration and healing capacity for round mandibular bone defects. This result was related to the fact that the bone defects in the 20 M rat group provided more favorable conditions for new bone regeneration.
衰老对颌面部骨缺损愈合能力的影响尚未得到研究。本研究的目的是评估衰老对下颌骨圆形骨缺损再生的影响。我们在不同年龄(2个月龄[2M]、10个月龄[10M]和20个月龄[20M])的大鼠下颌角区域制造了一个圆形骨缺损,并评估了这些组中的新骨再生情况。研究了骨转换标志物的变化,如碱性磷酸酶、I型前胶原N端前肽(PINP)、I型胶原交联C端肽和抗酒石酸酸性磷酸酶5B(TRAP5b)。20M组的骨体积/总体积和骨密度显著高于2M组(P = 0.029,0.019)。在20M组中观察到骨形成标志物PINP水平较低,在10M和20M组中观察到骨吸收标志物TRAP5b水平较高。微计算机断层扫描(µ-CT)结果显示,老年大鼠的骨形成明显高于年轻大鼠,血清PINP水平较低,TRAP5b水平较高。老年大鼠骨缺损的局部环境被增厚的骨组织包围,这可能影响了我们的研究结果。总之,老年大鼠对圆形下颌骨缺损表现出更强的新骨再生和愈合能力。这一结果与20M大鼠组的骨缺损为新骨再生提供了更有利的条件这一事实有关。