Skip navigation

DSpace

機構典藏 DSpace 系統致力於保存各式數位資料(如:文字、圖片、PDF)並使其易於取用。

點此認識 DSpace
DSpace logo
English
中文
  • 瀏覽論文
    • 校院系所
    • 出版年
    • 作者
    • 標題
    • 關鍵字
    • 指導教授
  • 搜尋 TDR
  • 授權 Q&A
    • 我的頁面
    • 接受 E-mail 通知
    • 編輯個人資料
  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/123456789/40476
完整後設資料紀錄
DC 欄位值語言
dc.contributor.advisor賈景山,郭生興
dc.contributor.authorTuan-Yu Kaoen
dc.contributor.author高端佑zh_TW
dc.date.accessioned2021-06-14T16:48:45Z-
dc.date.available2017-10-01
dc.date.copyright2011-10-03
dc.date.issued2011
dc.date.submitted2011-08-12
dc.identifier.citation1. Nanci A: , Ten Cate's Oral Histology Development, Structure, and Function 7th edition, Mosby Elsevier 319~357
2. Sonntag CF: The comparative anatomy of the tongues of the Mammalia XII. Summary, classification and phylogeny, Proc Zool Soc Lond 1925, 701-762
3. Livingston RM: Some observations on the natural history of the tongue, Ann R Coll Surg Engl 1956, 19:185-200
4. Cortopassi D, Muhl ZF: Videofluorographic analysis of tongue movement in the rabbit (Oryctolagus cuniculus), J Morphol 1990, 204:139-146
5. Zhang GH, Zhang HY, Deng SP, Qin YM: Regional differences in taste bud distribution and alpha-gustducin expression patterns in the mouse fungiform papilla, Chem Senses 2008, 33:357-362
6. Marshall D, Hardman MJ, Byrne C: SPRR1 gene induction and barrier formation occur as coordinated moving fronts in terminally differentiating epithelia, J Invest Dermatol 2000, 114:967-975
7. Sonis ST: Mucositis as a biological process: a new hypothesis for the development of chemotherapy-induced stomatotoxicity, Oral Oncol 1998, 34:39-43
8. Lockhart PB, Sonis ST: Relationship of oral complications to peripheral blood leukocyte and platelet counts in patients receiving cancer chemotherapy, Oral Surg Oral Med Oral Pathol 1979, 48:21-28
9. Smith KP, Luong MX, Stein GS: Pluripotency: toward a gold standard for human ES and iPS cells, J Cell Physiol 2009, 220:21-29
10. Paris F: Endothelial Apoptosis as the Primary Lesion Initiating Intestinal Radiation Damage in Mice, Science 2001, 293:293-297
11. Etiz D, Erkal HS, Serin M, Kucuk B, Hepari A, Elhan AH, Tulunay O, Cakmak A: Clinical and histopathological evaluation of sucralfate in prevention of oral mucositis induced by radiation therapy in patients with head and neck malignancies, Oral Oncol 2000, 36:116-120
12. Handschel J, Sunderkotter C, Prott FJ, Meyer U, Kruse-Losler B, Joos U: Increase of RM3/1-positive macrophages in radiation-induced oral mucositis, J Pathol 2001, 193:242-247
13. Bonan PRF, Kaminagakura E, Pires FR, Vargas PA, de Almeida OP: Histomorphometry and immunohistochemical features of grade I (WHO) oral radiomucositis, Oral Diseases 2007, 13:170-176
14. Sonis ST, Peterson RL, Edwards LJ, Lucey CA, Wang L, Mason L, Login G, Ymamkawa M, Moses G, Bouchard P, Hayes LL, Bedrosian C, Dorner AJ: Defining mechanisms of action of interleukin-11 on the progression of radiation-induced oral mucositis in hamsters, Oral Oncol 2000, 36:373-381
15. Logan RM, Gibson RJ, Sonis ST, Keefe DM: Nuclear factor-kappaB (NF-kappaB) and cyclooxygenase-2 (COX-2) expression in the oral mucosa following cancer chemotherapy, Oral Oncol 2007, 43:395-401
16. Sonis ST, Scherer J, Phelan S, Lucey CA, Barron JE, O'Donnell KE, Brennan RJ, Pan H, Busse P, Haley JD: The gene expression sequence of radiated mucosa in an animal mucositis model, Cell Prolif 2002, 35 Suppl 1:93-102
17. Sonis ST: The pathobiology of mucositis, Nature Reviews Cancer 2004, 4:277-284
18. Dorr W, Heider K, Spekl K: Reduction of oral mucositis by palifermin (rHuKGF): dose-effect of rHuKGF, Int J Radiat Biol 2005, 81:557-565
19. Sonis S, Haddad R, Posner M, Watkins B, Fey E, Morgan TV, Mookanamparambil L, Ramoni M: Gene expression changes in peripheral blood cells provide insight into the biological mechanisms associated with regimen-related toxicities in patients being treated for head and neck cancers, Oral Oncol 2007, 43:289-300
20. Mothersill C, Seymour CB: Radiation-induced bystander effects--implications for cancer, Nat Rev Cancer 2004, 4:158-164
21. Aprile G, Ramoni M, Keefe D, Sonis S: Application of distance matrices to define associations between acute toxicities in colorectal cancer patients receiving chemotherapy, Cancer 2008, 112:284-292
22. Denham JW, Hauer-Jensen M: The radiotherapeutic injury--a complex 'wound', Radiother Oncol 2002, 63:129-145
23. Criswell T, Leskov K, Miyamoto S, Luo G, Boothman DA: Transcription factors activated in mammalian cells after clinically relevant doses of ionizing radiation, Oncogene 2003, 22:5813-5827
24. Andrieu-Abadie N, Levade T: Sphingomyelin hydrolysis during apoptosis, Biochim Biophys Acta 2002, 1585:126-134
25. Sonis ST: The biologic role for nuclear factor-kappaB in disease and its potential involvement in mucosal injury associated with anti-neoplastic therapy, Crit Rev Oral Biol Med 2002, 13:380-389
26. Sonis ST: Mucositis: The impact, biology and therapeutic opportunities of oral mucositis, Oral Oncology 2009, 45:1015-1020
27. Frieling JT, Mulder JA, Hendriks T, Curfs JH, van der Linden CJ, Sauerwein RW: Differential induction of pro- and anti-inflammatory cytokines in whole blood by bacteria: effects of antibiotic treatment, Antimicrob Agents Chemother 1997, 41:1439-1443
28. Albrecht M, Muller K, Kohn FM, Meineke V, Mayerhofer A: Ionizing radiation induces degranulation of human mast cells and release of tryptase, International Journal of Radiation Biology 2007, 83:535-541
29. Sonis ST, O'Donnell KE, Popat R, Bragdon C, Phelan S, Cocks D, Epstein JB: The relationship between mucosal cyclooxygenase-2 (COX-2) expression and experimental radiation-induced mucositis, Oral Oncol 2004, 40:170-176
30. Tran KT, Griffith L, Wells A: Extracellular matrix signaling through growth factor receptors during wound healing, Wound Repair Regen 2004, 12:262-268
31. Basson MD: In vitro evidence for matrix regulation of intestinal epithelial biology during mucosal healing, Life Sci 2001, 69:3005-3018
32. Barasch A, Peterson DE: Risk factors for ulcerative oral mucositis in cancer patients: unanswered questions, Oral Oncol 2003, 39:91-100
33. Chansky K, Benedetti J, Macdonald JS: Differences in toxicity between men and women treated with 5-fluorouracil therapy for colorectal carcinoma, Cancer 2005, 103:1165-1171
34. Schwab M, Zanger UM, Marx C, Schaeffeler E, Klein K, Dippon J, Kerb R, Blievernicht J, Fischer J, Hofmann U, Bokemeyer C, Eichelbaum M: Role of Genetic and Nongenetic Factors for Fluorouracil Treatment-Related Severe Toxicity: A Prospective Clinical Trial by the German 5-FU Toxicity Study Group, Journal of Clinical Oncology 2008, 26:2131-2138
35. Bogunia-Kubik K, Polak M, Lange A: TNF polymorphisms are associated with toxic but not with aGVHD complications in the recipients of allogeneic sibling haematopoietic stem cell transplantation, Bone Marrow Transplantation 2003, 32:617-622
36. Ambrosone CB, Tian C, Ahn J, Kropp S, Helmbold I, von Fournier D, Haase W, Sautter-Bihl ML, Wenz F, Chang-Claude J: Genetic predictors of acute toxicities related to radiation therapy following lumpectomy for breast cancer: a case-series study, Breast Cancer Res 2006, 8:R40
37. Ostman A, Augsten M: Cancer-associated fibroblasts and tumor growth – bystanders turning into key players, Current Opinion in Genetics & Development 2009, 19:67-73
38. Bodey GP, Rodriguez V, Chang HY, Narboni: Fever and infection in leukemic patients: a study of 494 consecutive patients, Cancer 1978, 41:1610-1622
39. Donnelly J, Bellm L, Epstein J, Sonis S, Symonds R: Antimicrobial therapy to prevent or treat oral mucositis, The Lancet Infectious Diseases 2003, 3:405-412
40. El-Sayed S: Prophylaxis of Radiation-Associated Mucositis in Conventionally Treated Patients With Head and Neck Cancer: A Double-Blind, Phase III, Randomized, Controlled Trial Evaluating the Clinical Efficacy of an Antimicrobial Lozenge Using a Validated Mucositis Scoring System, Journal of Clinical Oncology 2002, 20:3956-3963
41. Rand KH, Kramer B, Johnson AC: Cancer chemotherapy associated symptomatic stomatitis: role of Herpes simplex virus (HSV), Cancer 1982, 50:1262-1265
42. Woo SB, Sonis ST, Sonis AL: The role of herpes simplex virus in the development of oral mucositis in bone marrow transplant recipients, Cancer 1990, 66:2375-2379
43. Djuric M, Jankovic L, Jovanovic T, Pavlica D, Brkic S, Knezevic A, Markovic D, Milasin J: Prevalence of oral herpes simplex virus reactivation in cancer patients: a comparison of different techniques of viral detection, Journal of Oral Pathology & Medicine 2008, 38:167-173
44. Raber-Durlacher JE, Elad S, Barasch A: Oral mucositis, Oral Oncology 2010, 46:452-456
45. Keefe DM, Schubert MM, Elting LS, Sonis ST, Epstein JB, Raber-Durlacher JE, Migliorati CA, McGuire DB, Hutchins RD, Peterson DE: Updated clinical practice guidelines for the prevention and treatment of mucositis, Cancer 2007, 109:820-831
46. Spielberger R, Stiff P, Bensinger W, Gentile T, Weisdorf D, Kewalramani T, Shea T, Yanovich S, Hansen K, Noga S, McCarty J, LeMaistre CF, Sung EC, Blazar BR, Elhardt D, Chen MG, Emmanouilides C: Palifermin for oral mucositis after intensive therapy for hematologic cancers, N Engl J Med 2004, 351:2590-2598
47. Barasch A, Epstein J, Tilashalski K: Palifermin for management of treatment-induced oral mucositis in cancer patients, Biologics 2009, 3:111-116
48. ClinicalTrials.gov: (http://clinicaltrials.gov/),
49. Tran CD, Sundar S, Howarth GS: Dietary zinc supplementation and methotrexate-induced small intestinal mucositis in metallothionein-knockout and wild-type mice, Cancer Biol Ther 2009, 8:1662-1667
50. Buchsel PC, Forgey A, Grape FB, Hamann SS: Granulocyte macrophage colony-stimulating factor: current practice and novel approaches, Clin J Oncol Nurs 2002, 6:198-205
51. Aspinall RJ, Pockros PJ: SCV-07 (SciClone Pharmaceuticals/Verta), Curr Opin Investig Drugs 2006, 7:180-185
52. Hunter A, Mahendra P, Wilson K, Fields P, Cook G, Peniket A, Crawley C, Hickling R, Marcus R: Treatment of oral mucositis after peripheral blood SCT with ATL-104 mouthwash: results from a randomized, double-blind, placebo-controlled trial, Bone Marrow Transplantation 2008, 43:563-569
53. Porozov S, Cahalon L, Weiser M, Branski D, Lider O, Oberbaum M: Inhibition of IL-1β and TNF-α Secretion from Resting and Activated Human Immunocytes by the Homeopathic Medication TraumeelR S, Clinical and Developmental Immunology 2004, 11:143-149
54. Keefe DM, Sonis ST, Bowen JM: Emerging drugs for chemotherapy-induced mucositis, Expert Opin Emerg Drugs 2008, 13:511-522
55. Dorr W, Spekl K, Martin M: Radiation-induced oral mucositis in mice: strain differences, Cell Prolif 2002, 35 Suppl 1:60-67
56. Muanza TM, Cotrim AP, McAuliffe M, Sowers AL, Baum BJ, Cook JA, Feldchtein F, Amazeen P, Coleman CN, Mitchell JB: Evaluation of radiation-induced oral mucositis by optical coherence tomography, Clin Cancer Res 2005, 11:5121-5127
57. Zheng C, Cotrim AP, Sunshine AN, Sugito T, Liu L, Sowers A, Mitchell JB, Baum BJ: Prevention of Radiation-Induced Oral Mucositis after Adenoviral Vector-Mediated Transfer of the Keratinocyte Growth Factor cDNA to Mouse Submandibular Glands, Clinical Cancer Research 2009, 15:4641-4648
58. Ryu SH, Kang KM, Moon SY, Chai GY, Hong JP, Cho KO, Kang MI, Choi EK, Lee SW: Therapeutic effects of recombinant human epidermal growth factor (rhEGF) in a murine model of concurrent chemo- and radiotherapy-induced oral mucositis, J Radiat Res (Tokyo) 2010, 51:595-601
59. Haagen J, Krohn H, Rollig S, Schmidt M, Wolfram K, Dorr W: Effect of selective inhibitors of inflammation on oral mucositis: Preclinical studies, Radiotherapy and Oncology 2009, 92:472-476
60. Li CY, Chen XH, Tao XA, Xia J, Cheng B: The development and inflammatory features of radiotherapy-induced glossitis in rats, Med Oral Patol Oral Cir Bucal 2011, 16:e348-353
61. Watkins B, Pouliot K, Fey E, Tuthill C, Sonis S: Attenuation of radiation- and chemoradiation-induced mucositis using gamma-d-glutamyl-l-tryptophan (SCV-07), Oral Diseases 2010, 16:655-660
62. Kitagawa J, Nasu M, Okumura H, Shibata A, Makino K, Terada H, Matsumoto S: Allopurinol gel mitigates radiation-induced mucositis and dermatitis, J Radiat Res (Tokyo) 2008, 49:49-54
63. Cassatt D, Fazenbaker C, Bachy C, Kifle G, McCarthy M: Amifostine (ETHYOL) protects rats from mucositis resulting from fractionated or hyperfractionated radiation exposure, International Journal of Radiation OncologyBiologyPhysics 2005, 61:901-907
64. Zang M, and Su CH: Ganoderma comphoratum, a new taxon in genus Ganoderma from Taiwan., China Acta Bot Yunnanica 1990, 12:395-396
65. Chang TT, Chou WN: Antrodia cinnamomea sp. nov. on Cinnamomum kanehirai in Taiwan, Mycol Res 1995, 99:750-758
66. Wu SH, Ryvarden L, Chang TT: Antrodia camphorate (“niu-chang-chih”), new combination of a medicinal fungus in Taiwan., Bot Bull Acad Sin 1997, 38:273-275
67. Chang TT, Chou WN: Antrodia cinnamomea reconsidered and A. salmonea sp. nov. on Cunninghamia konishii in Taiwan, Bot Bull Acad Sin 2004, 45:347-352
68. Tsai ZT, Liaw SL: The use and the effect of Ganoderma., Taichung 1985, 116-117
69. Hseu YC, Wu FY, Wu JJ, Chen JY, Chang WH, Lu FJ, Lai YC, Yang HL: Anti-inflammatory potential of Antrodia Camphorata through inhibition of iNOS, COX-2 and cytokines via the NF-kappaB pathway, Int Immunopharmacol 2005, 5:1914-1925
70. Ao ZH, Xu ZH, Lu ZM, Xu HY, Zhang XM, Dou WF: Niuchangchih (Antrodia camphorata) and its potential in treating liver diseases, J Ethnopharmacol 2009, 121:194-212
71. Hseu YC, Chen SC, Yech YJ, Wang L, Yang HL: Antioxidant activity of Antrodia camphorata on free radical-induced endothelial cell damage, J Ethnopharmacol 2008, 118:237-245
72. Hseu YC, Chang WC, Hseu YT, Lee CY, Yech YJ, Chen PC, Chen JY, Yang HL: Protection of oxidative damage by aqueous extract from Antrodia camphorata mycelia in normal human erythrocytes, Life Sci 2002, 71:469-482
73. Kuo MC, Chang CY, Cheng TL, Wu MJ: Immunomodulatory effect of Antrodia camphorata mycelia and culture filtrate, J Ethnopharmacol 2008, 120:196-203
74. Chen YJ, Cheng PC, Lin CN, Liao HF, Chen YY, Chen CC, Lee KM: Polysaccharides from Antrodia camphorata mycelia extracts possess immunomodulatory activity and inhibits infection of Schistosoma mansoni, Int Immunopharmacol 2008, 8:458-467
75. Shen YC, Chou CJ, Wang YH, Chen CF, Chou YC, Lu MK: Anti-inflammatory activity of the extracts from mycelia of Antrodia camphorata cultured with water-soluble fractions from five different Cinnamomum species, FEMS Microbiol Lett 2004, 231:137-143
76. Yang J, Liu X, Bhalla K, Kim CN, Ibrado AM, Cai J, Peng TI, Jones DP, Wang X: Prevention of apoptosis by Bcl-2: release of cytochrome c from mitochondria blocked, Science 1997, 275:1129-1132
77. Adams JM, Cory S: The Bcl-2 protein family: arbiters of cell survival, Science 1998, 281:1322-1326
78. Tewari M, Quan LT, O'Rourke K, Desnoyers S, Zeng Z, Beidler DR, Poirier GG, Salvesen GS, Dixit VM: Yama/CPP32 beta, a mammalian homolog of CED-3, is a CrmA-inhibitable protease that cleaves the death substrate poly(ADP-ribose) polymerase, Cell 1995, 81:801-809
79. Michael H. Ross, Pawlina W: Histology: A Text and Atlas: With Correlated Cell and Molecular Biology. Edited by Lippincott Williams & Wilkins, 2010, p.pp. 182~187
80. Abul K. Abbas M, Andrew H. Lichtman M, PhD, Shiv Pillai M: Cellular and Molecular Immunology. Edited by Saunders/Elsevier, 2009, p.pp. 446-447
81. Kenneth Murphy, Paul Travers, Walport M: Janeway's immunobiology. Edited by New York, Garland Science, 2008, p.pp. 567-568
82. Maltby S, Khazaie K, McNagny KM: Mast cells in tumor growth: angiogenesis, tissue remodelling and immune-modulation, Biochim Biophys Acta 2009, 1796:19-26
83. Galli SJ, Tsai M: Mast cells: versatile regulators of inflammation, tissue remodeling, host defense and homeostasis, J Dermatol Sci 2008, 49:7-19
84. Weller K, Foitzik K, Paus R, Syska W, Maurer M: Mast cells are required for normal healing of skin wounds in mice, FASEB J 2006, 20:2366-2368
85. Crivellato E, Beltrami CA, Mallardi F, Ribatti D: The mast cell: an active participant or an innocent bystander?, Histol Histopathol 2004, 19:259-270
86. Zheng H, Wang J, Hauer-Jensen M: Role of mast cells in early and delayed radiation injury in rat intestine, Radiat Res 2000, 153:533-539
87. Richter KK, Langberg CW, Sung CC, Hauer-Jensen M: Increased transforming growth factor beta (TGF-beta) immunoreactivity is independently associated with chronic injury in both consequential and primary radiation enteropathy, Int J Radiat Oncol Biol Phys 1997, 39:187-195
88. Boerma M, Wang J, Wondergem J, Joseph J, Qiu X, Kennedy RH, Hauer-Jensen M: Influence of mast cells on structural and functional manifestations of radiation-induced heart disease, Cancer Res 2005, 65:3100-3107
89. Watanabe S, Watanabe K, Oishi T, Aiba M, Kageyama K: Mast cells in the rat alveolar septa undergoing fibrosis after ionizing irradiation. Ultrastructural and histochemical studies, Lab Invest 1974, 31:555-567
90. Ward WF, Molteni A, Ts'ao CH, Hinz JM: Captopril reduces collagen and mast cell accumulation in irradiated rat lung, Int J Radiat Oncol Biol Phys 1990, 19:1405-1409
91. Dvorak AM: New aspects of mast cell biology, Int Arch Allergy Immunol 1997, 114:1-9
92. Sara Szabo, Swarajit N. Ghosh, Brian L. Fish, Sreedhar Bodiga, Rade Tomic, Gagan Kumar, Natalya V. Morrow, John E. Moulder, Jacobs ER, Medhora M: Cellular Inflammatory Infiltrate in Pneumonitis Induced by a Single Moderate Dose of Thoracic X Radiation in Rats, Radiation Research 2010, 173:545-556
93. Hsiao G, Shen MY, Lin KH, Lan MH, Wu LY, Chou DS, Lin CH, Su CH, Sheu JR: Antioxidative and hepatoprotective effects of Antrodia camphorata extract, J Agric Food Chem 2003, 51:3302-3308
94. You WC, Hsieh CC, Huang JT: Effect of extracts from indigowood root (Isatis indigotica Fort.) on immune responses in radiation-induced mucositis, J Altern Complement Med 2009, 15:771-778
95. Stokman MA, Spijkervet FK, Wymenga AN, Burlage FR, Timens W, Roodenburg JL, de Vries EG: Quantification of oral mucositis due to radiotherapy by determining viability and maturation of epithelial cells, J Oral Pathol Med 2002, 31:153-157
96. Dorr W, Hamilton CS, Boyd T, Reed B, Denham JW: Radiation-induced changes in cellularity and proliferation in human oral mucosa, Int J Radiat Oncol Biol Phys 2002, 52:911-917
97. Scully C, Epstein JB: Oral health care for the cancer patient, Eur J Cancer B Oral Oncol 1996, 32B:281-292
98. Brien TP, Farraye FA, Odze RD: Gastric dysplasia-like epithelial atypia associated with chemoradiotherapy for esophageal cancer: a clinicopathologic and immunohistochemical study of 15 cases, Mod Pathol 2001, 14:389-396
99. Kovesi G, Szende B: Changes in apoptosis and mitotic index, p53 and Ki67 expression in various types of oral leukoplakia, Oncology 2003, 65:331-336
100. Marijnen CA, Kapiteijn E, Nagtegaal ID, Mulder-Stapel AA, van de Velde CJ, Schrier PI, Peltenburg LT, van Krieken JH: p53 expression in human rectal tissue after radiotherapy: upregulation in normal mucosa versus functional loss in rectal carcinomas, Int J Radiat Oncol Biol Phys 2002, 52:720-728
101. Jiang YL, Escano MF, Sasaki R, Fujii S, Kusuhara S, Matsumoto A, Sugimura K, Negi A: Ionizing radiation induces a p53-dependent apoptotic mechanism in ARPE-19 cells, Jpn J Ophthalmol 2004, 48:106-114
102. Blirando K, Milliat F, Martelly I, Sabourin J-C, Benderitter M, Francois A: Mast Cells Are an Essential Component of Human Radiation Proctitis and Contribute to Experimental Colorectal Damage in Mice, The American Journal of Pathology 2011, 178:640-651
103. He SH: Key role of mast cells and their major secretory products in inflammatory bowel disease, World J Gastroenterol 2004, 10:309-318
104. Huaien Zheng: Role of Mast Cells in Early and Delayed Radiation Injury in Rat Intestine, Radiation Research 2000, 153:533-539
105. Tobita T, Izumi K, Feinberg SE: Development of an in vitro model for radiation-induced effects on oral keratinocytes, Int J Oral Maxillofac Surg 2010, 39:364-370
106. Malik IA, Moriconi F, Sheikh N, Naz N, Khan S, Dudas J, Mansuroglu T, Hess CF, Rave-Frank M, Christiansen H, Ramadori G: Single-dose gamma-irradiation induces up-regulation of chemokine gene expression and recruitment of granulocytes into the portal area but not into other regions of rat hepatic tissue, Am J Pathol 2010, 176:1801-1815
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/40476-
dc.description.abstract放射線照射引發口腔黏膜潰瘍是頭頸部癌症放射線治療中常見的副作用,但目前仍無有效的治療藥劑。臨床上的治療方法如給予含有麻醉劑的漱口藥水、維持好的口腔衛生、營養支持、感染控制、及給予角質細胞生長因子或輻射保護劑等支持性照護,上述方法雖然臨床上可達到部份的控制,然而卻無法經濟有效地以及於分子層級有針對性地減輕口腔黏膜潰瘍。發炎前驅物活性氧分子ROS及細胞激素IL-1β、TNF-α常見於口腔粘膜潰瘍組織中,證明口腔黏膜潰瘍是一種發炎相關疾病。牛樟芝Antrodia camphorata是台灣特有的傳統中草藥,具有抗發炎、抗氧化和免疫調節的功能。本實驗將建立小鼠吻部局部照射放射線單一劑量37.5 Gy所引發的口腔黏膜潰瘍模型,並以舌背黏膜為觀查對象,作為評估放射線引發口腔黏膜炎之臨床疾病理變化,以及觀察牛樟芝抗發炎作用緩解口腔潰瘍的有效性。實驗於放射線照射前五天起開始分別餵食水以及牛樟芝,並於照射後第0、3、6、9、12天分批犧牲小鼠,取其舌背黏膜作病理組織分析上皮厚度及肥大細胞,以及前發炎細胞激素基因的表現量偵測。實驗結果顯示,兩組小鼠體重於照射放射線後開始下降,但兩組無顯著差異;兩組舌背黏膜厚度普遍上都由舌根往舌尖方向依序遞減之現象,餵食牛樟芝組的平均舌背黏膜及舌頭各部位皆有比餵食水的組別更厚的趨勢;此外牛樟芝組亦有抑制肥大細胞數目增生或聚集的作用;發炎相關細胞激素基因表現的差異則不明顯;另外根據本實驗結果建立臨床小鼠之放射線引發口腔黏膜炎之分級方法。總結,本研究初步建立放射線治療引發口腔潰瘍之小鼠模型,此外餵食牛樟芝有緩和小鼠口腔黏膜炎的趨勢。zh_TW
dc.description.abstractRadiation-induced mucositis (RIM) is a common side effect of radiation therapy in head and neck cancer patients. So far, management has been directed to to supportive cares such as mouth rinse with anesthetics, nutritional support, infection treatment, or systemic administration of keratinocyte growth factor or radioprotectors. Whereas these interventions have been valuable for clinical management, they have not been efficiently or collectively directed to molecularly targeted prevention and treatment. RIM is an inflammation-associated disease, because reactive oxygen species and proinflammatory cytokine such as IL-1β and TNF-α were detected in mucositis tissue. Antrodia camphorata (AC) is a typical Chinese herb found only in Taiwan, and it has anti-inflammation, antioxidant and immunomodulatory properties. This study established a RIM mice model via local irradiation of single dose—37.5 Gy toward snout and observes the dorsal surface mucosa of tongue for evaluating the clinical and histopathological changes. Water or AC was feed from day 5 before iiradiation. After irradiated on day 0, each group of mice were sacrificed on day 0, 3, 6, 9, 12, and the tongue were incised for histopathological analysis of epithelial thickness, mast cells counts and pro-inflammatory cytokine gene expression. The body weight began to decline after radiation exposure, but there were no significant differences; epithelial thickness of dorsal surface mucosa revealed gradually descending amount of thickness from tongue posterior toward tip in both groups; AC group showed generalized thicker than the water group. In addition, AC group seemed to have the effect that inhibits mast cell hyperplasia or recruitment. Gene expression profiles of pro-inflammation cytokine showed no significant difference. We also established the grading system of dorsal surface mucosa in RIM mice model. In conclusion, the radiation induced mucositis mouse model was established and we founded that AC would ameliorate RIM in mice.en
dc.description.provenanceMade available in DSpace on 2021-06-14T16:48:45Z (GMT). No. of bitstreams: 1
ntu-100-R98422029-1.pdf: 253240613 bytes, checksum: 4593df919df2ebe60256db4376d21a70 (MD5)
Previous issue date: 2011
en
dc.description.tableofcontents口試委員會審定書 i
誌 謝 iii
中文摘要 v
ABSTRACT vii
目 錄 ix
圖目錄 xiii
表目錄 xv
附錄目錄 xvi
第1章 導論及文獻回顧 1
1.1 本章概要 1
1.2 口腔黏膜簡介 1
1.2.1 口腔黏膜之定義 1
1.2.2 口腔黏膜之增生與成熟 1
1.2.3 口腔黏膜之解剖構造 2
1.2.4 固有層之結構 2
1.2.5 小鼠舌背構造之簡介 2
1.3 口腔黏膜炎簡介 3
1.3.1 口腔黏膜炎發生機制之研究回顧 3
1.3.2 口腔黏膜炎發生之五階段模型 4
1.3.3 口腔黏膜炎之危險因子 8
1.3.4 口腔環境與口腔黏膜炎之關係 10
1.3.5 口腔黏膜炎之治療指引及未來研究方向 11
1.4 放射線引發黏膜炎於動物模型之回顧 12
1.5 牛樟芝簡介 13
1.5.1 命名及分類地位 13
1.5.2 牛樟芝型態特性 14
1.5.3 牛樟芝一般成份分析 15
1.5.4 生物功能活性研究 15
1.6 肥大細胞與放射線引發口腔黏膜炎之關係 19
1.6.1 肥大細胞簡介 19
1.6.2 肥大細胞與放射線引發口腔黏膜炎關係之回顧 20
1.6.3 肥大細胞與放射線引發腸道黏膜炎及肺炎關係之回顧 20
1.7 本實驗之研究動機 21
1.8 本實驗之研究主旨及目標 21
第2章 實驗材料與方法 23
2.1 本章概要 23
2.2 實驗動物 23
2.3 牛樟芝製備 23
2.3.1 牛樟芝來源 23
2.3.2 牛樟芝懸浮液製備 23
2.4 照射放射線 24
2.4.1 照射放射線之設備 24
2.4.2 照射放射線之方法 24
2.5 實驗用麻醉藥 25
2.5.1 若朋 25
2.5.2 舒泰 50 25
2.5.3 麻醉劑調配方式 25
2.6 實驗分組及流程 26
2.6.1 分組方式 26
2.6.2 實驗流程 26
2.7 檢體採集 26
2.7.1 檢體採集方式 26
2.7.2 檢體之固定與包埋 27
2.8 分析口腔黏膜炎之方法 27
2.8.1 觀察口腔黏膜炎之方法 27
2.8.2 切片拍照及分段方式 28
2.8.3 上皮層厚度之測量 28
2.9 組織染色 29
2.9.1 蘇木紫-伊紅染色 29
2.9.2 甲苯胺藍染色 29
2.10 訊息核糖核酸之抽取、反轉錄與定量 30
2.10.1 訊息核糖核酸之抽取與反轉 30
2.10.2 定量即時聚合酶連鎖反應 31
2.11 統計方法 31
第3章 實驗結果 33
3.1 本章概要 33
3.2 小鼠體重之變化趨勢 33
3.3 小鼠舌頭背側面之黏膜變化 34
3.4 小鼠舌背H&E染色切片之觀察比較 35
3.5 舌背黏膜厚度之變化趨勢 37
3.5.1 Vehicle組與AC組之厚度變化 37
3.5.2 Tongue posterior之厚度變化與比較 37
3.5.3 Tongue middle之厚度變化與比較 37
3.5.4 Tongue tip之厚度變化與比較 38
3.5.5 平均厚度之變化與比較 38
3.6 小鼠舌背toluidine blue染色切片之觀察比較 38
3.7 肥大細胞之變化趨勢 39
3.7.1 Vehicle組與AC組之變化 39
3.7.2 Tongue posterior之比較 39
3.7.3 Tongue middle之比較 40
3.7.4 Tongue tip之比較 40
3.7.5 肥大細胞總數之變化與比較 40
3.8 前發炎性細胞激素相關基因表現量 41
第4章 討論 43
4.1 本章概要 43
4.2 放射線引發口腔黏膜炎之舌黏膜外觀變化探討以及餵食牛樟芝之比較 43
4.2.1 分析方法之探討 43
4.2.2 實驗結果之探討 44
4.3 放射線引發口腔黏膜上皮層厚度變化以及餵食牛樟芝之比較 45
4.3.1 分析方法之探討 45
4.3.2 實驗結果之探討 47
4.4 肥大細胞於放射線引發口腔黏膜炎之探討以及餵食牛樟芝之比較 50
4.4.1 數量變化之探討 50
4.4.2 功能作用之探討 52
4.5 放射線引發口腔黏膜炎之發炎相關基因表現變化及餵食牛樟芝之比較 53
4.6 探討放射線引發口腔黏膜炎於小鼠模型之分級建立 54
參考文獻 55
圖 61
表 103
附錄 107
dc.language.isozh-TW
dc.subject放射線zh_TW
dc.subject口腔黏膜炎zh_TW
dc.subject小鼠模型zh_TW
dc.subjectmouse modelen
dc.subjectradiationen
dc.subjectoral mucositisen
dc.title建立放射線引發口腔潰瘍之小鼠模型及組織病理之分析zh_TW
dc.titleEstablishment and histopathological analysis of radiation induced mucositis mouse modelen
dc.typeThesis
dc.date.schoolyear99-2
dc.description.degree碩士
dc.contributor.oralexamcommittee成佳憲,江俊斌
dc.subject.keyword口腔黏膜炎,小鼠模型,放射線,zh_TW
dc.subject.keywordoral mucositis,mouse model,radiation,en
dc.relation.page123
dc.rights.note有償授權
dc.date.accepted2011-08-12
dc.contributor.author-college牙醫專業學院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

文件中的檔案:
檔案 大小格式 
ntu-100-1.pdf
  未授權公開取用
247.31 MBAdobe PDF
顯示文件簡單紀錄


系統中的文件,除了特別指名其著作權條款之外,均受到著作權保護,並且保留所有的權利。

社群連結
聯絡資訊
10617臺北市大安區羅斯福路四段1號
No.1 Sec.4, Roosevelt Rd., Taipei, Taiwan, R.O.C. 106
Tel: (02)33662353
Email: ntuetds@ntu.edu.tw
意見箱
相關連結
館藏目錄
國內圖書館整合查詢 MetaCat
臺大學術典藏 NTU Scholars
臺大圖書館數位典藏館
本站聲明
© NTU Library All Rights Reserved