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  1. NTU Theses and Dissertations Repository
  2. 醫學院
  3. 牙醫專業學院
  4. 臨床牙醫學研究所
請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/40999
完整後設資料紀錄
DC 欄位值語言
dc.contributor.advisor姚宗珍(Chung-Chen Jane Yao)
dc.contributor.authorYa-Hui Yangen
dc.contributor.author楊雅慧zh_TW
dc.date.accessioned2021-06-14T17:11:03Z-
dc.date.available2008-08-08
dc.date.copyright2008-08-08
dc.date.issued2008
dc.date.submitted2008-07-25
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32. Kruse-Losler B, Meyer U, Floren C, Joos U. Influence of distraction rates on the temporomandibular joint position and cartilage morphology in a rabbit model of mandibular lengthening. Journal of Oral & Maxillofacial Surgery 2001;59:1452-1459; discussion 1460-1451.
33. Liu ZJ, King GJ, Herring SW. Alterations of morphology and microdensity in the condyle after mandibular osteodistraction in the rat. Journal of Oral & Maxillofacial Surgery 2003;61:918-927.
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40. Weil TS, Van Sickels JE, Payne CJ. Distraction osteogenesis for correction of transverse mandibular deficiency: a preliminary report. Journal of Oral & Maxillofacial Surgery 1997;55:953-960.
41. Li KK, Powell NB, Riley RW. Distraction osteogenesis in adult obstructive sleep apnea surgery: A preliminary study. Journal of Oral & Maxillofacial Surgery 2002;60:6.
42. 曾慧. 生長期迷你豬施行單側下顎骨牽引性骨生成術之骨骼三度空間形態變化 臨床牙醫學研究所. 台北: 國立臺灣大學; 2003.
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44. 鄭位明, 王佩華, 章浩宏, 宋永義. 小耳種李宋系迷你豬乳齒萌發順序之研究. 中國畜牧學會會誌 1999;28:347-358.
45. Stuart A, Smith D. Use of the fluorochromes xylenol orange, calein green, and tetracycline to document bone deposition and remodeling in healing fractures in chickens. Avian diseases 1992;36:447-449.
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47. Roth S, Muller K, Fischer DC, Dannhauer KH. Specific properties of the extracellular chondroitin sulphate proteoglycans in the mandibular condylar growth centre in pigs. Archives of Oral Biology 1997;42:63-76.
48. Erben RG. Bone-labeling techniques. In: An YHKLM, editor. Handbook of histology methods for bone and cartilage. Totowa, New Jersey: Humana Press Inc.; 2003. p. 99-118.
49. Ghafari J, Heeley JD. Condylar adaptation to muscle alteration in the rat. Angle Orthodontist 1982;52:26-37.
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52. Meyer U, Kruse-Losler B, Meyer T, Joos U. Influence of distraction rates on compression-related degenerative alterations in temporomandibular joints. In: Diner PA VM, editor. 2nd International Congress on Cranial and Facial Bone Distraction Progress. Paris, France, Bologna, Italy: Monduzzi Editore; 1999.
53. Salter RB, Simmonds DF, Malcolm BW, Rumble EJ, MacMichael D, Clements ND. The biological effect of continuous passive motion on the healing of full-thickness defects in articular cartilage. An experimental investigation in the rabbit. Journal of Bone & Joint Surgery - American Volume 1980;62:1232-1251.
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55. Benske J, Schunke M, Tillmann B. Subchondral bone formation in arthrosis. Polychrome labeling studies in mice. Acta Orthopaedica Scandinavica 1988;59:536-541.
56. Nakai H, Niimi A, Ueda M. The influence of compressive loading on growth of cartilage of the mandibular condyle in vitro. Archives of Oral Biology 1998;43:505-515.
57. Tominaga K, Hirashima S, Fukuda J. An experimental model of osteoarthrosis of the temporomandibular joint in monkeys. British Journal of Oral & Maxillofacial Surgery 2002;40:232-237.
58. Mankin HJ. The response of articular cartilage to mechanical injury. Journal of Bone & Joint Surgery - American Volume 1982;64:460-466.
59. Hinton RJ, McNamara JA, Jr. Temporal bone adaptations in response to protrusive function in juvenile and young adult rhesus monkeys (Macaca mulatta). European Journal of Orthodontics 1984;6:155-174.
60. Troulis MJ, Glowacki J, Perrott DH, Kaban LB. Effects of latency and rate on bone formation in a porcine mandibular distraction model. Journal of Oral & Maxillofacial Surgery 2000;58:507-513; discussion 514.
61. Wehrbein H, Glatzmaier J, Yildirim M. Orthodontic anchorage capacity of short titanium screw implants in the maxilla. An experimental study in the dog. Clinical Oral Implants Research 1997;8:131-141.
62. Wehrbein H, Diedrich P. Endosseous titanium implants during and after orthodontic load--an experimental study in the dog. Clinical Oral Implants Research 1993;4:76-82.
63. Liou EJW, Pai BCJ, Lin JCY. Do miniscrews remain stationary under orthodontic forces? American Journal of Orthodontics & Dentofacial Orthopedics 2004;126:42-47.
64. Majzoub Z, Finotti M, Miotti F, Giardino R, Aldini NN, Cordioli G. Bone response to orthodontic loading of endosseous implants in the rabbit calvaria: early continuous distalizing forces. European Journal of Orthodontics 1999;21:223-230.
65. Gristina AG. Implant failure and the immuno-incompetent fibro-inflammatory zone. Clinical Orthopaedics & Related Research 1994:106-118.
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68. Sant'Anna EF, Gomez DF, Polley JW, Sumner RD, Williams JM, Figueroa AA et al. Histological evaluation of the temporomandibular joint after bilateral vertical ramus mandibular distraction in a canine model. Journal of Craniofacial Surgery 2007;18:155-162; discussion 163-154.
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/40999-
dc.description.abstract牽引性骨生成術(Distraction Osteogenesis)廣泛應用於治療成長期中顱顏部發育異常的病患,使之能夠提早建立正常的生理性功能。然而文獻中關於下顎牽引性骨生成術造成顳顎關節的變化尚無定論,其中又很少將生長因素列入考量。本實驗的目的即為以生長期迷你豬為實驗對象,探討下顎進行單側牽引性骨生成術後,顳顎關節骨質組織學的變化。
實驗共計6隻具有生長潛力的迷你豬(年齡分布為5週至12週大,處於混合齒列),分成三組:(1)實驗組A,n=1,實驗側施行單側下顎骨截斷並裝置口內延長器,術後經過7天的延遲期,每天以0.9公厘的速度逐漸延長下顎,共延長14天,延長完成後固定4週再進行犧牲。(2)實驗組B,n=2,延長完成後固定8週再進行犧牲,以觀察長期的變化。(3)控制組,n=1,以相同之規則進行牽引,開始牽引四天後,因牽引軸被豬隻撞落而無法繼續牽引,停止牽引後固定8週再進行犧牲;將之歸入控制組,以觀察同樣經過單側下顎骨截斷及放置口內延長器,但僅經過少量牽引,對顳顎關節影響之差異。(4)對照組,n=2,為與實驗組B犧牲時年齡相近的健康迷你豬,作為提供對照組織的對照。為了研究骨頭的動態變化,在實驗期間以皮下注射生物螢光染色劑的方式,進行活體的骨頭標定,再以倒立螢光顯微鏡觀察不同螢光層線之部位及分布,以觀察顳顎關節周圍骨質沈積的速率與部位。
研究結果發現,在關節軟骨下方的骨質,不論是實驗組或是對照組,由關節髁的前端到後端,都只看到在犧牲前所標定的calcein,只能顯現出成長中的豬隻,在整個下顎關節髁有相當旺盛的骨質沈積及代謝。然而在顳顎關節窩,卻可以發現到在靠近關節腔的部位,骨沈積的速率即使在固定期一個月及兩個月後,比對照組的骨沈積速率來的快,代表下顎的牽引延長,不僅外側關節髁頭受牽引的力量往關節窩接近,而影響關節髁及關節盂窩的形態、軟骨厚度及下方基質的分解,也會影響到顳顎關節窩的骨生成速率。
另外在牽引器的固定骨釘周圍,也發現大量的骨質吸收及發炎反應,而造成固定骨釘的提早鬆脫,無法提供良好的固定功能,因此無法將牽引的力量完全傳達至截斷骨的兩端,導致預期牽引量與實際牽引量產生落差。
因此,牽引性骨生成術能夠有效地延長下顎,對顳顎關節的形態及骨生成速率會產生影響,惟在形態上的變化以及可能對下顎運動功能的影響仍須更長期的追蹤觀察。
zh_TW
dc.description.abstractDistraction osteogenesis has been widely used in congenital anomalies to correct craniofacial deficiency. Clinically it is frequently conducted on growing patients for early establishment of normal physiological functions. However, the effects on temporomandibular joints undergoing mandibular distraction are still controversial, and the influence of growth was not taken into consideration in most of the research. In this study, we investigated the effects on bone remodeling of TMJs in growing mini-pigs in which unilateral mandibular distraction osteogenesis was performed.
Six (5~12 weeks, 6~15kg weight) Lee-Sung genus of mini-pigs were divided into 4 groups: 1) Experimental group A (n=1), received osteotomy and the distractor device (Leibinger intraoral distractor) was fixed on one side of the mandible. After one-week latency period, the mandible was distracted for 2 weeks with the velocity of 0.9 mm/day. The animals were sacrificed after a consolidation period of 4 weeks. 2) Experimental group B (n=2), the animals received the similar treatment as Experimental group A, except that they were sacrificed after a consolidation period of 8 weeks. 3) Control group (n=1), the distraction was little for the distractor was broken after 4 days of distraction. And 4) Normal group, 2 healthy mini-pigs without any operation were used. To examine the changes of bone remodeling of TMJs, polychrome labeling of bone was performed.
According to the bone labeling, the bone deposition and remodeling in the TMJs was very active during the entire experimental period. The thickness of cartilage of condyles decreased after 4 weeks of consolidation period, and it didn’t return to normal after 4 weeks later. The bone deposition of the glenoid fossa was more active in the experimental group then in the normal and control groups after 4 or 8 weeks of consolidation period. These findings revealed not only the condyle but also the glenoid fossa adapt to the distraction. Remarkable bone resorption around the fixation screws of distractors was also noted. Therefore, they cannot provide enough stability during the distraction.
In conclusion, distraction osteogenesis is an effective way to lengthen the mandible with subtle and transient changes in bone remodeling of TMJ. A longer-term observation will reveal whether these changes would last and affect the mandibular movement and function.
en
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en
dc.description.tableofcontents第一章 前言 1
1.1 牽引性骨生成術的發展及應用 1
1.1.1 牽引性骨生成術的發展 1
1.1.2 牽引器的分類 2
1.1.3 牽引性骨生成術在下顎骨的應用 3
1.2 牽引對周圍組織的影響 4
1.3 牽引對顳顎關節的影響 6
1.3.1 下顎牽引對顳顎關節的影響--動物實驗 6
1.3.2 下顎牽引對顳顎關節的影響--臨床研究 11
1.4 本系列研究先前之結果 11
第二章 實驗目的 13
第三章 材料與方法 14
3.1 研究材料 14
3.2 實驗設計與分組 14
3.3 手術過程 15
3.4 骨頭螢光標定 (Polychrome labeling of bone) 16
3.4.1原理 16
3.4.2螢光染色劑 17
3.4.3螢光染色劑標定的時間 17
3.5 犧牲過程 17
3.6 牽引量記錄 18
3.7 標本製備及包埋 18
3.8 螢光顯微鏡觀察及影像擷取 19
3.9 穿透光觀測和軟骨厚度的測量 20
3.10 甲苯胺藍(toluidine blue)染色及組織學觀察 20
第四章 結果 22
4.1 牽引量及中線偏移 22
4.2 牙齒的螢光表現 23
4.3 顳顎關節的螢光表現 25
4.3.1 對照組的螢光表現 25
4.3.2 控制組的螢光表現 30
4.3.3 實驗組的螢光表現 34
4.4 參考骨釘及固定骨釘周圍之組織學變化 45
4.4.1 參考骨釘(P35 左側下顎骨體) 46
4.4.2 固定骨釘 49
第五章 討論 62
5.1 實驗方法之檢討及改良 62
5.1.1 動物模型的選取 62
5.1.2 螢光染色劑的標定 64
5.2 顳顎關節的變化 65
5.2.1 關節軟骨的變化 65
5.2.2 關節髁軟骨下方骨質變化 68
5.2.3 關節盂窩的骨質變化 70
5.3 實際牽引量未達預期之探討 73
5.4 固定骨釘受力後周圍骨質的變化 75
第六章 結論 77
附錄 78
參考文獻 91
dc.language.isozh-TW
dc.subject顳顎關節zh_TW
dc.subject牽引性骨生成術zh_TW
dc.subject迷你豬zh_TW
dc.subject骨頭螢光標定zh_TW
dc.subjectmini-pigen
dc.subjectdistraction osteogenesisen
dc.subjectpolychrome labelingen
dc.subjecttemporomandibular jointen
dc.title生長期迷你豬施行單側下顎骨牽引性骨生成術之顳顎關節骨質組織學觀察zh_TW
dc.titleHistological changes of bone in TMJs Following Mandibular Distraction Osteogenesis in Growing Mini-Pigsen
dc.typeThesis
dc.date.schoolyear96-2
dc.description.degree碩士
dc.contributor.oralexamcommittee陳韻之(Alex Yunn-Jy Chen),許明倫(Ming-Lun Hsu)
dc.subject.keyword牽引性骨生成術,迷你豬,顳顎關節,骨頭螢光標定,zh_TW
dc.subject.keyworddistraction osteogenesis,mini-pig,temporomandibular joint,polychrome labeling,en
dc.relation.page96
dc.rights.note有償授權
dc.date.accepted2008-07-28
dc.contributor.author-college醫學院zh_TW
dc.contributor.author-dept臨床牙醫學研究所zh_TW
顯示於系所單位:臨床牙醫學研究所

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