論文使用權限 Thesis access permission:校內校外均不公開 not available
開放時間 Available:
校內 Campus:永不公開 not available
校外 Off-campus:永不公開 not available
論文名稱 Title |
藻類及海羊齒乙酸乙酯粗萃液調節peroxisome proliferator response element表現之初步研究 Preliminary study on the expression of peroxisome proliferator response element by ethyl acetate extract of algae and Echinodermata Crinoidea |
||
系所名稱 Department |
|||
畢業學年期 Year, semester |
語文別 Language |
||
學位類別 Degree |
頁數 Number of pages |
80 |
|
研究生 Author |
|||
指導教授 Advisor |
|||
召集委員 Convenor |
|||
口試委員 Advisory Committee |
|||
口試日期 Date of Exam |
2009-03-14 |
繳交日期 Date of Submission |
2009-07-30 |
關鍵字 Keywords |
藻、萃取 PPAR, Luciferase, MTT |
||
統計 Statistics |
本論文已被瀏覽 5730 次,被下載 0 次 The thesis/dissertation has been browsed 5730 times, has been downloaded 0 times. |
中文摘要 |
PPAR (peroxisome proliferator activated receptors)為調控脂質代謝相關酵素基因之轉錄因子,與PPRE (peroxisome proliferator response element)作用可促進或抑制基因表現。本研究以建構於肝癌細胞(Huh-7)之PPRE-Luciferase 偵測不同藻類及海羊齒乙酸乙酯萃粗取物對PPAR/PPRE 之影響,並以(3-(4,5-imethylthiazol-2-yl)-2,5- diphenyltetrazolium bromide, MTT )進行細胞活性分析以區別細胞毒性之差異。大型藻類,龍鬚菜(Gracilaria coronopifolia J. Agardh)粗萃取物具有促進PPRE 效應且沒有細胞毒性。石花菜之細翼枝菜(Pterocladiella capillacea Santelices)與日本石花菜(Gelidium japonicum Okamura)及麒麟菜(Euchema sp.)粗萃取物具有促進PPRE 效應但卻有細胞毒性。安曼司石花菜(Gelidium amansii Lamouroux)粗萃物沒有PPRE 效應且沒有細胞毒性。紫菜(Porphyra sp.)粗萃取液抑制PPRE 效應且有細胞毒性。微細藻類,南寶公司提供之冷凍乾燥螺旋藻類 (spirulina sp.)粉粗萃物具促進PPRE 效應,且不具細胞毒性。由輔英科技大學周德珍老師提供之小球藻粗萃物會抑制PPRE 效應,卻不具細胞毒性。海洋齒(Echinodermata sp.) 粗萃物具有殺死蚊子幼蟲孑孓(toxicity)及防止蚊子接近(repellent)效果,但沒有PPRE 效應且沒有細胞毒性。本研究指出不同藻類及海洋齒具有不同之PPRE 效應及細胞毒性,龍鬚菜及螺旋藻具有PPRE調控之開發價值,海洋齒則有有綠色農藥之潛力。 |
Abstract |
PPAR (peroxisome proliferator activated receptors) is a transcription factor that regulates activity and transcription of enzymes of lipid metabolism and thought PPAR-PPRE (peroxisome proliferator activated receptors – peroxisome prolierator response element) interaction. Cell toxicity was also tested by (3-(4,5-dimethylthiaz ol-2-yl)-2,5-diphenyltetrazolium bromide (MTT assay)). The effects of ethyl acetate (EA) extracts of algae and Echinodermata sp. on PPRE-luciferase activity in Huh-7 cell and cell cytotoxicity were conducted. EA extracts of Gracilaria coronopifolia can induce PPRE-luciferase activity without cytotoxity. EA extracts of Pterocladiella capillacea, Gelidium japonicum, and Euchema sp. showed PPRE-luciferase activity and cytotoxicity. Gelidium amansii and Porphyra sp. did not show PPRE-Luciferase activity but had cyotoxicity. EA extracts of Spirulina sp. had PPRE-Luciferase activity but no cytotoxicity, while that of Chlorella sorokiniana inhibited PPRE-Luciferase activity but did not show cytotoxicity. EA extracts of Echinodermata sp. can kill larva and repellent of mosquito, but had no PPRE-Luciferase activity and cytotoxicity. These results demonstrated that the effects of EA extracts on PPRE-luciferase activity are different between algae. EA extract of Gracilaria and Spirulina showed PPRE regulation activity and Echinodermata sp. EA extract have the potential to become green chemical. |
目次 Table of Contents |
謝辭----------------------------------------------------------------i 中文摘要----------------------------------------------------------ii 英文摘要----------------------------------------------------------iii 目錄----------------------------------------------------------------iv 圖目錄-------------------------------------------------------------v 表目錄-------------------------------------------------------------ix 附錄目錄----------------------------------------------------------x 縮寫字對照-------------------------------------------------------xi 一、前言----------------------------------------------------------1 二、實驗進行之策略-------------------------------------------7 三、實驗流程圖-------------------------------------------------7 四、材料與方法-------------------------------------------------8 五、結果----------------------------------------------------------17 六、討論----------------------------------------------------------21 七、參考文獻----------------------------------------------------27 八、附錄----------------------------------------------------------53 |
參考文獻 References |
行政院農委會漁業署 87-96年度漁業年報,台灣,中華民國。 行政院衛生署95年度全民健康保險醫療統計年報,台灣,中華民國。 孫乃云,2005,石花菜水萃取液抗氧化及抗癌活性之探討,國立台灣海洋大學水產養殖學系碩士論文,台灣,中華民國。 Berger, J., Moller, D.E., 2002. The mechanisms of action of PPARs. Annual Review of Medicine 53, 409-435. Bradford, M.M., 1976. A rapid and sensitive method for quantitation of microgram quantities of protein utilizing the principle of protein-dye-binding. Analytical Biochemistry 72, 248-254. Brun, R.P., Kim, J.B., Hu, E., M., S.B., 1997. Peroxisome proliferator-activated receptor gamma and the control of adipogenesis. Current Opinion in Lipidology 8, 212-218. Carr, A., Workman, C., Carey, D., Rogers, G., Martin, A., Baker, D., Wand, H., Law, M., Samaras, K., Emery, S., Coope, D.A., 2004. No effect of rosiglitazone for treatment of HIV-1 lipoatrophy: randomised, double-blind, placebo-controlled trial. Lancet 363, 429-438. Carter, A.B., A.Misyak, S., Hontecillas, R., Bassaganya-Riera, J., 2009. Dietary modulation of inflammation-induced colorectal cancer through PPARγ. PPAR Research 2009, 1-9. Chio, E.H., 2007. A quick insecticide bioassay with mosquitoes. Formosan Entomol 27, 183-188. Chou, Y.-C., Prakash, E., Huang, C.-F., Lien, T.-W., Chen, X., Su, I.-J., Chao, Y.-S., Hsieh, H.-P., Hsu, J.T.-A., 2008. Bioassay-guided purification and identification of PPAR α/γ agonists from Chlorella sorokiniana. Phytotherapy Research 22, 605-613. Desvergne, B.a., Wahli, W., 1999. Peroxisome proliferator-activated receptors: nuclear control of metabolism. Endocrine Reviews 20, 649-688. Ford, E.S., Giles, W.H., Dietz, W.H., 2002. Prevalence of the metabolic syndrome among US adults: findings from the third national health and nutrition examination survey. The Journal of the American Medical Association 287, 356-359. Gottlicher, M., Widmark, E., Li, Q., Gustafsson, J.A., 1992. Fatty-acids activate a chimera of the clofibric acid-activated receptor and the glucocorticoid receptor. Proceedings of the National Academy of Sciences of the United States of America 89, 4653-4657. Grundy, S.M., Becker, D., Clark, L.T., Cooper, R.S., Denke, M.A., Howard, W.J., Hunninghake, D.B., Illingworth, D.R., Luepker, R.V., McBride, P., McKenney, J.M., Pasternak, R.C., Stone, N.J., Horn, L.V., 2002. Third report of the national cholesterol education program expert panel on detection evaluation and treatment of high blood chloesterol in adults final report. Circulation 106, 3143-3421. Haffner, S., Valdez, R., Hazuda, H., Mitchell, B., orales, P., Stern, M., 1992. Prospective analysis of the insulin-resistance syndrome (syndrome X). Diabetes 41, 715-722. Hess, R., staubli, W., Riess, W., 1965. Nature of the hepatomegalic effect produced by ethyl-hlorophenoxy-isobutyrate in the rat. Nature 208, 856-858. Hosokawa, M., Kudo, M., Maeda, H., Kohno, H., Tanaka, T., Miyashita, K., 2004. Fucoxanthin induces apoptosis and enhances the antiproliferative effect of the PPARγ ligand, troglitazone, on colon cancer cells. Biochimica et Biophysica Acta 1675, 113-119. Issemann, I., Green, S., 1990. Activation of a member of the steroid hormone receptor superfamily by peroxisome proliferators. Nature 347, 645-650. Kaplan, N.M., 1989. The deadly quartet. Upper-body obesity, glucose intolerance, hypertriglyceridemia, and hypertension. Archives of Internal Medicine 149, 1514-1520. Krey, G., Braissant, O., Horset, F.L., Kalkhoven, E., Perroud, M., Parker, M.G., Wahli, W., 1997. Fatty acids, eicosanoids, and hypolipidemic agents identified as ligands of peroxisome proliferator- activated receptors by coactivator-dependent receptor ligand assay. Molecular Endocrinology 11, 779-791. Kusunoki, J., Kanatani, A., Moller, D.E., 2006. Modulation of fatty acid metabolism as a potential approach to the treatment of obesity and the metabolic syndrome. Endocrine 29, 91-100. Latruffe, N., Vamecq, J., 1997. Peroxisome proliferators and peroxisome proliferator activated receptors (PPARs) as regulators of lipid metabolism. Biochimie 79, 81-94. Maeda, H., Hosokawa, M., Sashima, T., Funayama, K., Miyashita, K., 2005. Fucoxanthin from edible seaweed, Undaria pinnatifida, shows antiobesity effect through UCP1 expression in white adipose tissues. Biochemical and Biophysical Research Communications 332, 392-397. Maeda, H., Hosokawa, M., Sashima, T., Takahashi, N., Kawada, T., Miyashita, K., 2006. Fucoxanthin and its metabolite, fucoxanthinol, suppress adipocyte differentiation in 3T3-L1 cells. International Journal of Molecular Medicine 18, 147-152. Mannaerts, G.P., Van Veldhoven, P.P., 1993. Metabolic pathways in mammalian peroxisomes. Biochimie 75, 147-158. Marx, N., Sukhova, G.K., Collins, T., Libby, P., Plutzky, J., 1999. PPAR activators inhibit cytokine-induced vascular cell adhesion molecule-1 expression in human endothelial cells. Circulation 99, 3125-3131. Mora, F.D., Jones, D.K., Desai, P.V., Patny, A., Avery, M.A., Feller, D.R., Smillie, T., Zhou, Y.-D., Nagle, D.G., 2006. Bioassay for the identification of natural product-based activators of peroxisome proliferator-activated receptor-γ(PPARγ): The marine sponge metabolite psammaplin A activates PPARγ and induces apoptosis in human breast tumor cells. Journal of Natural Products 69, 547-552. Osumi, T., Wen, J.-K., Hashimoto, T., 1991. Two cis-acting regulatory sequences in the peroxisome proliferator-responsive enhancer region of rat acyl-CoA oxidase gene. Biochemical and Biophysical Research Communications 175, 866-871. Reaven, G.M., 1988. Banting lecture 1988. Role of insulin resistance in human disease. Diabetes 37, 1595-1607. Rival, Y., Benéteau, N., Taillandier, T., Pezet, M., Dupont-Passelaigue, E., Patoiseau, J.-F., Junquéro, D., Colpaert, F.C., Delhon, A., 2002. PPARα and PPARδ activators inhibit cytokine-induced nuclear translocation of NF-κB and expression of VCAM-1 in EAhy926 endothelial cells. European Journal of Pharmacology 435, 143-151. Rocchi, S., Picard, F., Vamecq, J., Gelman, L., NoellePotier, Zeyer, D., Dubuquoy, L., Bac, P., Champy, M.-F., Plunket, K.D., Leesnitzer, L.M., Blanchard, S.G., Desreumaux, P., Moras, D., Renaud, J.-P., Auwerx, J., 2001. A unique PPARγ ligand with potent insulin-sensitizing yet weak adipogenic activity. Molecular Cell 8, 737-747. Tontonoz, P., Hu, E.D., Spiegelman, B.M., 1994. Stimulation of adipogenesis in fibroblasts by PPAR-γ-2, a lipid-activated transcription factor. Cell 79, 1147-1156. Tugwood, J.D., Issemann, I., Anderson, R.G., Bundell, K.R., McPheat, W.L., Green, S., 1992. The mouse peroxisome proliferator activated receptor recognizes a response element in the 5' flanking sequence of the rat acyl-CoA oxidase gene. European Molecular Biology Organization Journal 11, 433-439. Yamamoto, Y., Nakajima, M., Yamazaki, H., Yokoi, T., 2001. Cytotoxicity and apoptosis produced by troglitazone in human hepatoma cells. Life Sciences 70, 471-482. |
電子全文 Fulltext |
本電子全文僅授權使用者為學術研究之目的,進行個人非營利性質之檢索、閱讀、列印。請遵守中華民國著作權法之相關規定,切勿任意重製、散佈、改作、轉貼、播送,以免觸法。 論文使用權限 Thesis access permission:校內校外均不公開 not available 開放時間 Available: 校內 Campus:永不公開 not available 校外 Off-campus:永不公開 not available 您的 IP(校外) 位址是 3.23.59.187 論文開放下載的時間是 校外不公開 Your IP address is 3.23.59.187 This thesis will be available to you on Indicate off-campus access is not available. |
紙本論文 Printed copies |
紙本論文的公開資訊在102學年度以後相對較為完整。如果需要查詢101學年度以前的紙本論文公開資訊,請聯繫圖資處紙本論文服務櫃台。如有不便之處敬請見諒。 開放時間 available 已公開 available |
QR Code |