Muhonen Arja, Muhonen Jarkko, Minn Heikki, Kulmala Jarmo, Klossner Jorma, Teräs Mika, Knuuti Juhani, Happonen Risto-Pekka
Department of Oral and Maxillofacial Surgery, University of Turku, FIN-20520, Turku, Finland.
Arch Oral Biol. 2002 Oct;47(10):701-7. doi: 10.1016/s0003-9969(02)00051-1.
[18F-]fluoride positron-emission tomography (PET) was used to assess bone formation during mandibular distraction osteogenesis. There were three study groups: irradiation, irradiation+hyperbaric oxygen and control. The two experimental groups received a tumoricidal dose of irradiation to the mandible, and one group was also given hyperbaric oxygen (2.5 ATA (atmospheres absolute) for 90 min) 18 times preoperatively. Control animals received neither irradiation nor oxygen. A unilateral osteotomy was made and, after a period of latency, bone distraction was started, continued for 2 weeks, and the distraction generated was then allowed to consolidate for 4 weeks. The first PET study was performed at the end of distraction and the second at the end of consolidation. At the end of distraction, the metabolic activity of bone in the distracted area was significantly higher in the controls than in either experimental group; differences between the experimental groups were not statistically significant. By the end of consolidation, activity in the control group had diminished to the same as in the two experimental groups, in which no significant change had occurred. Radioactivity was still significantly higher at second imaging on the distracted than non-distracted side in the control and irradiation+hyperbaric oxygen groups, but not in the group that was only irradiated. The results indicate that previous irradiation disturbs bone formation during mandibular distraction osteogenesis. Hyperbaric oxygen was not able to prevent the suppression of osteogenesis caused by radiotherapy but it might improve bone formation by prolonging high osteogenic activity.
[18F]氟化物正电子发射断层扫描(PET)用于评估下颌骨牵张成骨过程中的骨形成情况。研究分为三组:放疗组、放疗+高压氧组和对照组。两个实验组接受了对下颌骨的肿瘤杀伤剂量放疗,其中一组在术前还接受了18次高压氧治疗(2.5个绝对大气压,持续90分钟)。对照动物既未接受放疗也未接受吸氧。进行单侧截骨术,经过一段潜伏期后开始骨牵张,持续2周,然后让牵张产生的骨段巩固4周。第一次PET研究在牵张结束时进行,第二次在巩固结束时进行。在牵张结束时,对照组牵张区域骨的代谢活性显著高于两个实验组;实验组之间的差异无统计学意义。到巩固结束时,对照组的活性已降至与两个实验组相同的水平,而两个实验组的活性未发生显著变化。在对照组和放疗+高压氧组中,第二次成像时牵张侧的放射性仍显著高于未牵张侧,但仅接受放疗的组中并非如此。结果表明,先前的放疗会干扰下颌骨牵张成骨过程中的骨形成。高压氧不能预防放疗引起的成骨抑制,但可能通过延长高成骨活性来改善骨形成。