跳到主要內容

臺灣博碩士論文加值系統

(98.82.140.17) 您好!臺灣時間:2024/09/10 12:30
字體大小: 字級放大   字級縮小   預設字形  
回查詢結果 :::

詳目顯示

: 
twitterline
研究生:劉婕
研究生(外文):Jie Liu
論文名稱:黃柏在治療異位性皮膚炎中的應用
論文名稱(外文):Application of Huang Bo in Treating Atopic Dermatitis
指導教授:賴政宏賴政宏引用關係
指導教授(外文):Cheng-Hung Lai
口試委員:董光中詹昆衛
口試委員(外文):Kwong -Chung TungKun-Wei Chan
口試日期:2017-01-13
學位類別:碩士
校院名稱:國立中興大學
系所名稱:獸醫學系所
學門:獸醫學門
學類:獸醫學類
論文種類:學術論文
論文出版年:2017
畢業學年度:105
語文別:中文
論文頁數:87
中文關鍵詞:黃柏異位性皮膚炎
外文關鍵詞:Huang BoAtopic Dermatitis
相關次數:
  • 被引用被引用:0
  • 點閱點閱:562
  • 評分評分:
  • 下載下載:125
  • 收藏至我的研究室書目清單書目收藏:0
異位性皮膚炎(atopic dermatitis; AD)屬於慢性、復發性、炎症性並伴隨著強烈搔抓、潮紅病灶的皮膚疾病。它是一種皮膚的過度免疫,主要由於炎症細胞受到各種過敏反應的活化所造成。黃柏是一種常用的傳統中草藥,近年來有越來越多的相關研究指出,黃柏具有一定的抑制細胞免疫反應和抗炎性作用,常常作為治療異位性皮膚炎的重要的藥物成分之一。本實驗之目的為評估黃柏對於誘導異位性皮膚炎大鼠之治療效用,並針對三種不同的給藥劑量進行治療效力差異性的比較。
實驗動物為25只雄性、七周齡之Sprague Dawley品系大鼠,利用化學性半抗原(haptens):2,4-二硝基氯苯(2,4-dinitrochlorobenzene; DNCB)試劑,一周兩次塗抹於大鼠背頸部皮膚,以達到誘導異位性皮膚炎的狀態,並維持誘導處置至實驗結束,共六周。誘導成功後,操作組按體重分別給予150 mg/kg,300 mg/kg,600 mg/kg的順天堂黃柏濃縮散灌胃治療,每週兩次,持續四周,四周後進行大鼠犧牲。本實驗進行評估的項目包括:皮膚炎臨床狀態評分、皮膚鏡觀察、血清總IgE抗體力價、皮膚組織切片H&E(Hematoxylin-Eosin)染色下之表皮厚度及炎症細胞之浸潤情形、皮膚組織切片TB(Toluidine Blue)染色下肥大細胞之浸潤情形。
結果顯示,黃柏治療的組別在表皮厚度與炎症細胞浸潤計數的部分,與陽性控制組相比,三組皆有不同程度的下降(P<0.05);在肥大細胞浸潤計數的部分,與陽性控制組相比,三組皆有下降的趨勢,但僅中等劑量組和高等劑量組有顯著性差異(P<0.05);在皮膚炎臨床狀態評分數值上,與陽性控制組相比,治療組皆有顯著性下降(P<0.05),但在組內比較上,低等劑量組的皮膚炎臨床狀態評分數值在治療前後數值雖有下降,差異卻不顯著;在IgE 數值上,與陽性控制組相比,三組皆有下降的趨勢,但僅中等劑量組和高等劑量組有顯著性差異(P<0.05)。體重改變在黃柏治療的組別與陽性控制組之間,不存在顯著性差異(P>0.05)。實驗過程中亦無產生其他明顯異常或副作用。
本實驗結果顯示黃柏的治療可以減輕異位性皮膚炎的病程變化、調節免疫系統並緩解皮膚發炎的情形,並且治療效果隨著藥物劑量的增加而變得更好。
中草藥治療異位性皮膚炎本身具有副作用少、安全性高等優點,在證明黃柏治療異位性皮膚炎的效果後,期許未來可以更多加應用在獸醫臨床治療的領域中。
Atopic Dermatitis (AD) is a kind of skin disease, because of excessive immunity of skin mainly due to the activation of inflammatory cells by all kinds of allergic reactions. Huang Bo, which contain Cortex Phellodendri as the main ingredients, has the ability of immunosuppression and anti-inflammatory, which could inhibit the growth of a variety of bacteria. The aim of this study is to evaluate the effect of Huang Bo in treating rats suffered from AD, and compare the difference between the effects of three doses Huang Bo.
A total of 25 7-week-old male SD rats, were treated with chemical haptens (2, 4-dinitrochlorobenzene; DNCB) on the bank to induce AD for a total of six weeks. After successfully induced AD, the rats of treatment groups were given 150 mg/kg, 300 mg/kg, 600 mg/kg of Huang Bo by i.g. for 4 weeks. The evaluating projects in this experiment contain Dermatitis Score, serum total Ig E levels and skin histological characteristics including epidermis thickness, infiltration of inflammatory cells, and the infiltration of mast cell infiltration.
As aresult, compared with the positive control group, there was a decrease of the degree of epidermal thickness and inflammatory cell infiltration in the treatment of Huang Bo. The mast cell infiltration count decreased in the three groups compared with the positive control group. Treatment with Huang Bo can significantly decrease the Dermatitis Score. In the IgE values, there was a decreasing trend in the three treatment groups compared with the positive control group. No other significant abnormalities or side effects were observed during the course of the experiment.
The results of this study support that being treated with Huang Bo can reduce the course of atopic dermatitis changes, regulate the immune system and relieve skin inflammation, and the treatment effect becomes better as dose increasing.
誌謝 1
摘要 i
Abstract iii
第一章 緒言 1
第二章 文獻探討 4
第一節 異位性皮膚炎 4
一、 異位性皮膚炎之定義 4
二、 異位性皮膚炎之病因及致病機制 5
三、 犬、貓異位性皮膚炎於臨床上傳統治療方式 7
四、 誘導異位性皮膚炎之實驗動物模型 11
五、 異位性皮膚炎改善效力之評估 15
第二節 黃柏 20
一、 中醫上對異位性皮膚炎病因的看法 20
二、 黃柏的化學成分 20
三、 黃柏的藥理作用 23
四、 黃柏對小鼠 DTH 及其體內幾種細胞因數的影響 29
第三章 材料與方法 31
第一節 實驗動物 31
第二節 實驗材料 31
一、 實驗藥物與試劑 31
二、 實驗儀器與設備 32
三、 其他 33
第三節 實驗設計 33
一、 實驗分組 33
二、 藥物劑量的選擇 34
三、 建立異位元性皮膚炎模型 35
四、 異位性皮膚炎改善效力之評估 36
第四節 資料分析 40
第四章 結果 42
第一節 臨床狀態觀察 42
第二節 血清總IgE抗體力價檢測 43
第三節 皮膚狀態觀察與皮膚炎臨床狀態評分 45
第四節 皮膚組織切片H&E染色下皮膚厚度觀察 47
第五節 皮膚組織切片H&E染色下炎症細胞之浸潤情形 48
第六節 皮膚組織切片TB染色下肥大細胞之浸潤情形 49
第五章 討論 50
第一節 誘導效果評估 50
第二節 治療評估-血清總IgE抗體力價檢測 51
第三節 治療評估-皮膚炎臨床狀態評分 53
第四節 治療評估-皮膚厚度、皮膚組織切片H&E及TB染色 55
一、 皮膚組織切片 H&E 染色下皮膚厚度 55
二、 皮膚組織切片H&E染色下炎症細胞之浸潤 56
三、 皮膚組織切片TB染色下肥大細胞之浸潤 56
第六章 結論 58
參考文獻 60
附錄圖表 74
丁紅濤,顏瑜。中藥黃柏粉配合紅黴素治療72例子宮頸炎患者的臨床療效分析。中外醫療:28-29,2013。
中華本草編委會。中華本草(精選本上冊):1042,1998。
孔令東,楊澄,仇熙。黃柏炮製品清除氧自由基和抗脂質過氧化作用。中國中藥雜誌,245,2001。
王小燕,劉麗,陳光亮。二妙散及其衍生方的現代研究概況。時珍國醫國藥,105-106,2006。
王利。三妙散的鎮痛抗炎作用實驗研究。中獸醫學雜誌 142:16-18,2008。
王思謙。複方黃柏液保留灌腸治療大腸濕熱型潰瘍性結腸炎臨床研究。湖北中醫藥大學,2012。
王飛,郭力。加味三妙膠囊及黃柏對前列腺滲透作用的實驗觀察。成都醫藥29:42,2003。
王萌,吉騰飛,楊建波。川黃柏化學成分研究。中藥材,2: 208-210,2009。
王萌。常用中藥川黃柏和黃連化學成分及生物活性比較研究。北京協和醫學院研究生院,2009。
王楠楠,汪冶,楊建瓊。禿葉黃皮樹葉子的化學成分研究。天然產物研究與開發22:419-421,2010。
王德全,胡俊英。黃柏膠囊抗炎療效臨床分析。中華實用中西雜誌 4: 839,2004。
丘珍,王嘉英,呂紅斌。行氣消腫類中藥對體外培養的軟骨細胞代謝的影響。中國運動醫學雜誌17:34-37,1998。
同心。消化系統疾病的漢方治療: 黃柏提取物的抗潰瘍效果。國外醫學•中醫中藥分冊 18: 34,1996。
呂燕甯邱全瑛。黃柏對小鼠DTH及其體內幾種細胞因數的影響。北京中醫藥大學學報,48-50,1999。
呂嬪果,陳朝良。複方黃柏液換藥治療皮肌炎皮膚潰爛的療效觀察。海峽藥學25:100-101,2013。
宋雅梅,李智。防己黃柏凝膠鎮痛抗炎藥理作用研究。遼寧中醫學院學報,7-8,2006。
李中輝,魏躍鋼。中藥大青葉、黃柏、龍膽草對小鼠皮膚炎症反應的影響。中國麻風皮膚病雜誌第31卷第5期,288-291,2015。
李丹丹,江培,楊書美,高尚。黃柏的化學成分、藥理作用及臨床應用研究進展。黑龍江醫藥。601-605,2004。
李元紅。複方黃柏液皮膚科新用。中國中醫急診,672,2006。
李敬峰,張鵬飛,姜紅英。複方黃柏液保留灌腸治療潰瘍性結腸炎的療效。實用臨床醫學14:12-14,2013。
杜平化,朱世真,呂品。20種藥材對幽門螺桿菌體外抗菌活性的研究。中藥材,188,2001。
周道洪,沈元珊,趙曼瑞。測定淋巴細胞轉化和鼠白細胞介素2活性的新方法——MTT比色法。中國免疫學雜誌,39-44,1986。
邱全瑛,譚允育,趙岩松,康娟娟,張希林。黃柏和小檗堿對小鼠免疫功能的影響。中國病理生理雜誌:664-664。1996。
范積平,張貞良,廖曉玲。不同產地黃柏藥材中4種主要生物鹼類成分的含量測定。廣東藥學院學報,54-57,2010。
烏日娜,都日娜。黃柏的研究進展。中國民族醫藥雜誌,75-76,2008。
秦民堅,王橫奇。黃皮樹樹皮的化學成分研究。林產化學與工業23:42-46,2003。
國家藥典委員會。中華人民共和國藥典:287,2010。
張志軍。黃柏提取物的抗潰瘍效果。國外醫學•中醫中藥分冊16: 29,1994。
張義虎,孫靜。黃柏的臨床應用總述。中國醫學創新7:182-183,2010
郭志堅,郭書好,何康明。黃柏葉中黃酮醇苷含量測定及其抑菌實驗。暨南大學學報(自然科學版),64,2002。
郭金銘,馮曉娟,宋立江,徐穎,劉長青。白速消皮膚黏膜消毒液亞急性毒性研究。職業與健康,2049-2051,2009。
陳蕾,邸大琳。黃柏體外抑菌作用研究。時珍國醫國藥17:759-760,2006。
黃超培,覃輝豔,王彥武,趙鵬。黃柏洗消劑的安全性試驗觀察。中國消毒學雜誌:281-282,2010。
楊澄,朱繼孝,王穎,等。鹽制對黃柏抗痛風作用的影響。中國中藥雜誌30:145,2005。
楊磊,張延英,李卉,萬學中,吳建軍。 黃柏煎劑的抗炎,抗菌作用研究。實驗動物科學4:14-17,2014。
賈紅慧,王曙,袁潔,李代英,勾倞。比較兩種黃柏組方二妙膠囊的抗炎作用。華西藥學雜誌 22:619-621,2007。
廖靜,鄂征,聶毓秀。中藥黃柏的光敏抗癌作用研究,首都醫科大學學報20:153-155,1999。
趙子劍。黃柏與蒼術共煎對黃柏中小檗堿提取率的影響實驗。中華中醫藥學刊27:1237-1238,2009。
趙向忠,董群。不同劑量黃柏組方大補陰丸(湯)對CJ小鼠IL-2/IL-4免疫調節作用的初步研究。皖南醫學院學報24:164-166,2005。
劉玉東。異位性皮膚炎的病因探討。中外健康文摘:377-378,2010。
劉壽山。中藥研究文獻摘要:608-614,1963。
蔡寶昌,潘揚,吳皓。國外天然藥物抗病毒研究簡況 19: 48,1997。
Alenius H, Laouini D, Woodward A, Mizoguchi E, Bhan AK, Castigli E, Geha RS. Mast cells regulate IFN-γ expression in the skin and circulating IgE levels in allergen-induced skin inflammation. Journal of Allergy and Clinical Immunology, 109: 106-113. 2002.
Barnes PJ. How corticosteroids control inflammation: Quintiles Prize Lecture 2005. British Journal of Pharmacology, 148: 245–254, 2006.
Cardini F, Weixin H. Moxibustion for correction of breech presentation: a randomized controlled trial. JAMA, 280: 1580-1584, 1998.
Chan CL, Hon LE, Leung PC, Sam SW, Fung KP, Lee YH, Lau YA. Traditional Chinese medicine for atopic eczema: PentaHerbs formula suppresses inflammatory mediators release from mast cells. Journal of Ethnopharmacology, 120: 85-91, 2008.
Chen FP, Chen TJ, Kung YY, Chen YC, Chou LF, Chen FJ, Hwang SJ. Use frequency of traditional Chinese medicine in Taiwan. BMC Health Services Research, 7: 726, 2007.
Chen G, Li KK, Fung CH, Liu CL, Wong HL, Leung PC, Ko CH. Er-Miao-San, a traditional herbal formula containing Rhizoma Atractylodis and Cortex Phellodendri inhibits inflammatory mediators in LPS-stimulated RAW264. 7 macrophages through inhibition of NF-κB pathway and MAPKs activation. Journal of Ethnopharmacology, 154: 711-718. 2014.
Chiu SW, Wang ZM, Leung TM, Moore D. Nutritional value of Ganoderma extract and assessment of its genotoxicity and antigenotoxicity using comet assays of mouse lymphocytes. Food and Chemical Toxicology, 38: 173–178, 2000.
Choi JK, Kim SH. Inhibitory effect of galangin on atopic dermatitis-like skin lesions. Food and Chemical Toxicology, 68: 135-141. 2014.
Choi JK, Kim SH. Rutin suppresses atopic dermatitis and allergic contact dermatitis. Experimental Biology and Medicine 238: 410-417, 2013.
Choi YY, Kim MH, Kim JH, Jung HS, Sohn Y, Choi YJ, Hwang MK, Kim SH, Kim J, Yang WM. Schizonepeta tenuifolia inhibits the development of atopic dermatitis in mice. Phytotherapy Research, 27: 1131-1135, 2013.
Choi YY, Kim MH, Lee JY, Hong J, Kim SH, Yang WM. Topical application of Kochia scoparia inhibits the development of contact dermatitis in mice. Journal of Ethnopharmacology, 154: 380-385, 2014.
Coca AF, Cooke RA. On the classification of the phenomena of hypersensitiveness. The Journal of Immunology, 8: 163-182,1923.
Spergel JM., Mizoguchi E, Oettgen H, Bhan AK, Geha RS. Roles of T H 1 and T H 2 cytokines in a murine model of allergic dermatitis. The Journal of Clinical Investigation, 103: 1103-1111, 1999.
Davidson P, Hancock K, Leung D, Ang E, Chang E, Thompson DR, Daly J. Traditional Chinese medicine and heart disease: what does Western medicine and nursing science know about it? European Journal of Cardiovascular Nursing, 2: 171–181, 2003.
DeBoer DJ. Canine atopic dermatitis: new targets, new therapies. The Journal of Nutrition, 134: 2056-2061, 2004.
Del RJ, Friedlander SF.. Corticosteroids: options in the era of steroid-sparing therapy. Journal of the American Academy of Dermatology, 53: 50-58, 2005
Eisenberg DM, Davis RB, Ettner SL, Appel S, Wilkey S, Van RM, Kessler RC. Trends in alternative medicine use in the United States 1990–1997: results of a follow-up national survey. The Journal of the American Medical Association, 280: 1569–1575. 1998.
Eskinazi, DP. Factors that shape alternative medicinep. The Journal of the American Medical Association, 280: 1621–1623, 1998.
Fartasch M. pidermal barrier in disorders of the skin. Microsc Res Tech: 361-372, 1997.
Forrest S, Dunn K, Elliott K, Fitzpatrick E, Fullerton J, McCarthy M, Brown J, Hill D, Williamson R. Identifying genes predisposing to atopic eczema. Journal of Allergy and Clinical Immunology, 104: 1066-1070, 1999.
Geha RS. Allergy and hypersensitivity: nature versus nurture in allergy and hypersensitivity. Current Opinion in Immunology, 15: 603-608, 2003.
Hanifin JM, Chan SC, Cheng JB, Tofte SJ, Henderson WR Jr, Kirby DS, Weiner ES. Type 4 phosphodiesterase inhibitors have clinical and in vitro anti-inflammatory effects in atopic dermatitis. Journal of Investigative Dermatology, 107: 51-56, 1996.
Hattori T, Yamada S, Furuta K. [Studies on anti-nephritic effects of plant components (5). Effects of pherodendrin on original and crescentic-type anti-GBM nephritis in rats].Nihon yakurigaku zasshi. Folia Pharmacologica Japonica, 99: 391-399, 1992.
Hnilica KA. Small animal dermatology: a color atlas and therapeutic guide. Elsevier Health Sciences, 2010.
Ho YW, Yeung JS, Chiu PK, Tang WM, Lin ZB., Man RY, Lau CS. Ganoderma lucidum polysaccharide peptide reduced the production of proinflammatory cytokines in activated rheumatoid synovial fibroblast. Molecular and Cellular Biochemistry, 301: 173–179. 2007
Howell MD, Jones JF, Kisich KO, Streib JE, Gallo RL, Leung DY. Selective killing of vaccinia virus by LL-37: implications for eczema vaccinatum. The Journal of Immunology, 172: 1763-1767, 2004.
Hu YM, Su GH, Sze SCW, Ye W, Tong Y. Quality assessment of Cortex Phellodendri by high‐performance liquid chromatography coupled with electrospray ionization mass spectrometry. Biomedical Chromatography, 24: 438-453, 2010.
Huang CH, Kuo IC, Xu H, Lee YS, Chua KY. Mite allergen induces allergic dermatitis with concomitant neurogenic inflammation in mouse. Journal of Investigative Dermatology, 121: 289-293, 2003.
Huang YY, Chen AC, Carroll JD, Hamblin MR. Biphasic dose response in low level light therapy. Dose Response, 7: 358-583, 2009.
Ikuta A, Nakamura T, Vrabe H. Indolopyridoquinazoline, furoquinoline and canthinone type alkaloids from Phellodendron amurense callus tissues. Phytochemistry, 48: 285-291, 1998.
Jin H, He R, Oyoshi M, Geha RS. Animal models of atopic dermatitis. Journal of Investigative Dermatology, 129: 31-40, 2009.
Kawaguchi H, Kim M, Ishida M, Ahn YJ, Yamamoto T, Yamaoka R, Takahashi S. Several antifeedants from Phellodendron amurense against Reticulitermes speratus. Agricultural and Biological Chemistry, 53: 2635-2640, 1989.
Kawakami T, Ando T, Kimura M, Wilson BS, Kawakami Y. Mast cells in atopic dermatitis. Current Opinion in Immunology, 21: 666-678, 2009.
Kert J, Rose L. Clinical laser therapy – low level laser therapy. Ballerup, Denmark Scandinavian Medical Laser Technology: 146-150, 1989.
Kim GD, Lee SE, Park YS, Shin DH, Park GG, Park CS. Immunosuppressive effects of fisetin against dinitrofluorobenzene-induced atopic dermatitis-like symptoms in NC/Nga mice. Food and Chemical Toxicology: 341-349, 2014.
Kim MC, Lee CH, Yook TH. Effects of anti-inflammatory and Rehmanniae radix pharmacopuncture on atopic dermatitis in NC/Nga mice. Journal of Acupuncture and Meridian Studies, 6: 98-109, 2013.
Kim SH, Kim EK, Choi EJ. High-intensity swimming exercise increases dust mite extract and 1-Chloro-2,4-dinitrobenzene-derived atopic dermatitis in BALB/c mice. Inflammation, 37: 1179-1185, 2014.
Kim SJ, Kim YY, Ko KH, Hong EK, Han YB, Kang BH, Kim H. Butanol extract of 1: 1 mixture of Phellodendron cortex and Aralia cortex stimulates PI3‐kinase and ERK2 with increase of glycogen levels in HepG2 cells. Phytotherapy Research, 12: 255-260, 1998.
Kimura M, Tsuruta S, Yoshida T. Correlation of house dust mite–specific lymphocyte proliferation with IL-5 production, eosinophilia, and the severity of symptoms in infants with atopic dermatitis. Journal of Allergy and Clinical Immunology, 101(1), 84-89, 1998.
Kishi K, Yoshikawa K, Arihara S. Limonoids and protolimonoids from the fruits of Phellodendron amurense. Phytochemistry, 31: 1335-1338, 1992.
Kline JN. Pathogen recognition and new insights into innate immunity. Allergy Frontiers: Classification and Pathomechanisms. Springer Japan, 19-30, 2009.
Kondo K, Nagami T, Teramoto S. Differences in hematopoietic death among inbred strains of mice. Nagoya Univ. Japan,: 20-29, 1969.
Lam FY, KoWM, Ng SK, Tam LS, Leung PC, Li KM. Analgesic and anti-arthritic effects of Lingzhi and San Miao San supplementation in a rat model of arthritis induced by Freund’s complete adjuvant. Journal of Ethnopharmacology, 120: 44–50, 2008.
Laouini D, Alenius H, Bryce P, Oettgen H, Tsitsikov E, Geha RS. IL-10 is critical for Th2 responses in a murine model of allergic dermatitis. The Journal of Clinical Investigation, 112: 1058-1066, 2003.
Lee MS, Choi TY, Shin BC, Han CH, Ernst E. Cupping for stroke rehabilitation: a systematic review. Journal of the Neurological Sciences, 294: 70-73, 2010.
Lee SY. Atopic Dermatitis. The Korean Academy of Family Medicine, ed. Textbook of Family Medicine. 1st ed, Hankook Book, Seoul: 1265-1270, 2007.
Lennie TA. Relationship of body energy status to inflammation-induced anorexia andweight loss. Physiology and Behavior, 64: 475-481, 1998.
Leung DY, Bieber T, Atopic dermatitis, Lancet 361: 151-160, 2003.
Leung DY, Diaz LA, DeLeo V, Soter NA. Allergic and immunologic skin disorders. Allergic and Immunologic Skin Disorders. JAMA, 278: 1914-1923, 1997.
Lim HM, Lew KK, Tay DK. A clinical investigation of the efficacy of low level laser therapy in reducing orthodontic postadjustment pain. American Journal of Orthodontics and Dentofacial Orthopedics, 108: 614-622, 1995.
Lis A, Zdrojewska A. Chemical Composition of the Essential Oil From Fruits of Phellodendron chinense CK Schneid. Journal of Essential Oil Research, 21: 231-234, 2009.
Liu FT, Goodarzi H, Chen HY. IgE, mast cells, and eosinophils in atopic dermatitis. Clinical Reviews in Allergy and Immunology 41: 298-310, 2011.
Ma W, Tong H, Xu W, Hu J, Liu N, Li H, Cao L. Perivascular space: possible anatomical substrate for the meridian. The Journal of Alternative and Complementary Medicine, 9: 851-859, 2003.
Matsuda H, Watanabe N, Geba GP, Sperl J, Tsudzuki M, Hiroi J, Matsumoto M, Ushio H, Saito S, Askenase PW , Ra C. Development of atopic dermatitis-like skin lesion with IgE hyperproduction in NC/Nga mice. International Immunology, 9): 461-466, 1997.
Matsumoto K, Mizukoshi K, Oyobikawa M, Ohshima H, Tagami H. Establishment of an atopicdermatitis-like skin model in a hairless mouse by repeated elicitation of contact hypersensitivity thatenables to conduct functional analyses of the stratum corneum with various non-invasive biophysical instruments. Skin Research and Technology, 10: 122-129, 2004.
Morar N, Cookson WO, Harper JI, Moffatt MF. Filaggrin mutations in children with severe atopic dermatitis. Journal of Investigative Dermatology, 127: 1667-1672, 2007.
Mori H, Fuchigami M, Inoue N, Nagai H, Koda A, Nishioka I, Meguro K. Principle of the bark of Phellodendron amurense to suppress the cellular immune response: effect of phellodendrine on cellular and humoral immune responses. Planta Medica, 61, 45-49, 1995.
Mori H, Fuchigami M, Inoue N, Nagai H, Koda A, Nishioka I. Principle of the bark of Phellodendron amurense to suppress the cellular immune response. Planta Medica, 60: 445-449, 1994.
Napadow V, Ahn A, Longhurst J, Lao L, Stener-Victorin E, Harris R, Langevin HM, Nomura T, Sandilands A, Akiyama M, Liao H, Evans AT, Sakai K, Palmer CN. Unique mutations in the filaggrin gene in Japanese patients with ichthyosis vulgaris and atopic dermatitis. Journal of Allergy and Clinical Immunology, 119: 434-440, 2007.
Nedoszytko B, Sokołowska WM, Ruckemann DK, Roszkiewicz J, Nowicki RJ. Chemokines and cytokines network in the pathogenesis of the inflammatory skin diseases: atopic dermatitis, psoriasis and skin mastocytosis. Postepy Dermatologii I Alergologii, 31, 84-91, 2014.
Novak N, Bieber T, Leung DY. Immune mechanism leading to atopic dermatitis. Journal of Allergy and Clinical Immunology, 112: 128-139, 2003.
Nuttall T, Harvey RG, McKeever PJ. Canine atopic dermatitis. In: Nuttall T, Harvey RG, McKeever PJ, ed. A colour handbook of skin diseases of the dog and cat, 2nd ed,66 Manson Publishing, London, 20-30, 2009.
Olivry T, Mueller RS. Evidence-based veterinary dermatology: a systematic review of the pharmacology of canine atopic dermatitis. Veterinary dermatology, 14: 121-146, 2003.
Palmer CN, Irvine AD, Terron-Kwiatkowski A, Zhao Y, Liao H, Lee SP, Goudie DR, Sandilands A, Campbell LE, Smith FJ, O'Regan GM, Watson RM, Cecil JE,Bale SJ, Compton JG, DiGiovanna JJ, Fleckman P, Lewis-Jones S, Arseculeratne G, Sergeant A, Munro CS, El Houate B, McElreavey K, Halkjaer LB, Bisgaard H, Mukhopadhyay S, McLean WH. Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis. Nature Genetics 38: 441-446, 2006.
Pastore S, Fanales-Belasio E, Albanesi C, Chinni LM, Giannetti A, Girolomoni G. Granulocyte macrophage colony-stimulating factor is overproduced bykeratinocytes in atopic dermatitis. Implications for sustained dendritic cell activation in the skin. Journal of Clinical Investigation, 99: 3009-3017, 1997.
Rousseaux-Prevost R, Capron M, Bazin H, Capron A. IgE in experimental schistosomiasis. II. Quantitative determination of specific IgE antibodies against S. mansoni: a follow-up study of two strains of infected rats. Correlation with protective immunity. Immunology, 35: 33, 1978.
Ruud J, Wilhelms DB, Nilsson A, Eskilsson A, Tang YJ, Ströhle P, Caesar R, Schwaninger M, Wunderlich T, Bäckhed F, Engblom D, Inflammation-and tumor-induced anorexia and weight loss require MyD88 in hematopoietic/myeloid cells but not in brain endothelial or neural cells. The FASEB Journal, 27, 1973-1980, 2013.
Sampson HA. The evaluation and management of food allergy in atopic dermatitis. Clinics in Dermatology 21: 183-192., 2003.
Seicol NH. Consequences of cupping. New England Journal of Medicine, 335: 1281-1281, 1997.
Shintani F. Immunity and allergy disease. Shintani F, ed. Steps to internal medicine. Jungdam Publisher, Seoul, 3-27, 2005.
Spergel JM, Mizoguchi E, Brewer JP, Martin TR, Bhan AK, Geha RS. Epicutaneous sensitization with protein antigen induces localized allergicdermatitis and hyperresponsiveness to methacholine after single exposure to aerosolized antigen in mice. The Journal of Clinical Investigation, 101: 1614-1622, 1998.
Spergel JM, Mizoguchi E, Oettgen H, Bhan AK, Geha RS. Roles of TH1 and TH2
Sridharan G, Shankar AA. Toluidine blue: a review of its chemistry and clinical utility. Journal of Oral and Maxillofacial Pathology,16: 251, 2012.
Suen LK, Wong TK, Chung JW, Yip VY. Auriculotherapy on low back pain in the elderly. Complementary Therapies in Clinical Practice,13: 63-69, 2007.
Sung YY, Lee AY, Kim HK. Forsythia suspensa fruit extracts and the constituent matairesinol confer anti-allergic effects in an allergic dermatitis mouse model. Journal of Ethnopharmacology 187: 49-56, 2016.
Surh YJ, Chun KS, Cha HH, Han SS, Keum YS, Park KK, Lee SS. Molecular mechanisms underlying chemopreventive activities of anti-inflammatory phytochemicals: down-regulation of COX-2 and iNOS through suppression of NF-κB activation. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, 480: 243-268, 2001.
Taieb A, Wallach D, Tilles G. The history of atopic eczema/dermatitis. Handbook of atopic eczema. Springer Berlin Heidelberg: 10-20, 2006.
Thorpe SC, Murdoch RD, Kemeny DM. The effect of the castor bean toxin, ricin, on rat IgE and IgG responses. Immunology, 68: 307-311, 1989.
Trautmann A, Akdis M, Kleemann D, Altznauer F, Simon HU, Graeve T, Noll M, Bröcker EB, Blaser K,Akdis CA. T cell-mediated Fas-induced keratinocyte apoptosis plays a keypathogenetic role in eczematous dermatitis. The Journal of Clinical Investigation, 106: 25-35, 2000.
Vocanson M, Hennino A, Cluzel-Tailhardat M, Saint-Mezard P, Benetiere J, Chavagnac C, Berard F, Kaiserlian D, Nicolas JF. CD8+ T cells are effector cells of contact dermatitis to common skin allergens in mice. Journal of Investigative Dermatology, 126: 815-820, 2006.
Wakita H, Sakamoto T, Tokura Y, Takigawa M. E‐selectin and vascular cell adhesion molecule‐1 as critical adhesion molecules for infiltration of T lymphocytes and eosinophils in atopic dermatitis. Journal of Cutaneous Pathology, 21: 33-39, 1994.
Wong HC, Wong NY, Wong JK. Moxibustion for breech presentation. Complementary Therapies in Nursing and Midwifery, 6: 176-179, 1999.
Xian YF, Mao QQ, Ip SP, Lin ZX, Che CT. Comparison on the anti-inflammatory effect of Cortex Phellodendri Chinensis and Cortex Phellodendri Amurensis in 12-O-tetradecanoyl- -phorbol-13-acetate-induced ear edema in mice. Journal of Ethnopharmacology 137: 1425–1430, 2011.
Yamamoto M, Haruna T, Ueda C, Asano Y, Takahashi H, Iduhara M, Takaki S, Yasui K, Matsuo Y,Arimura A. Contribution of itch-associated scratch behavior to the development of skin lesions in Dermatophagoides farinae-induced dermatitis model in NC/Nga mice. Archives of Dermatological Research, 301: 739-746, 2009.
Yamamoto M, Haruna T, Yasui K, Takahashi H, Iduhara M, Takaki S, Deguchi M, Arimura A. A novel atopic dermatitis model induced by topical application with dermatophagoides farinae extract in NC/Nga mice. Allergology International, 56: 139-148, 2012.
Yang JH, Yoo JM, Cho WK, Ma JY. Ethanol Extract of Sanguisorbae Radix Inhibits Mast Cell Degranulation and Suppresses 2, 4-Dinitrochlorobenzene-Induced Atopic Dermatitis-Like Skin Lesions. Mediators of Inflammation,2016, 2016.
Yonekawa H, Takada T, Shitara H, Taya C, Matsushima Y, Matsuoka K, Kikkawa Y. Mouse Models for atopic dermatitis developed in japan. INTECH Open Access Publisher, 2012.
連結至畢業學校之論文網頁點我開啟連結
註: 此連結為研究生畢業學校所提供,不一定有電子全文可供下載,若連結有誤,請點選上方之〝勘誤回報〞功能,我們會盡快修正,謝謝!
QRCODE
 
 
 
 
 
                                                                                                                                                                                                                                                                                                                                                                                                               
第一頁 上一頁 下一頁 最後一頁 top