Taipei Medical University Institutional Repository:Item 987654321/51011
English  |  正體中文  |  简体中文  |  Items with full text/Total items : 45422/58598 (78%)
Visitors : 2548803      Online Users : 189
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version
    Please use this identifier to cite or link to this item: http://libir.tmu.edu.tw/handle/987654321/51011


    Title: 以D型半乳糖誘導老化動物模式評估之天然物抗氧化活性研究
    Study on Antioxidant Activities of Natural Products in D-Galatose-Induced Aging Mice
    Authors: 李泰霖
    Lee, Tai-Lin
    Keywords: d型半乳糖;薑黃素;老化;氧化壓力;d-galactose;curcumin;aging;oxidative stress
    Date: 2012-07-19
    Issue Date: 2018-10-05 10:09:14 (UTC+8)
    Abstract: 薑黃素 (curcumin) 是植物薑黃 (turmeric) 內主要具活性的成分,包含抗發炎、抗氧化、神經保護等活性。本篇研究探討薑黃素及其二十三個結構衍生物改善D型半乳糖誘導之老化鼠學習記憶能力及其抗氧化活性。經由細胞存活率測試 (Resazurin assay) ,發現結構衍生物七號及八號在10 ?嵱下對於以6-羥基多巴胺誘導人類母細胞瘤SH-SY5Y之神經毒性有顯著的保護作用。在同樣的條件下,也發現結構衍生物七號及八號有抑制細胞內ROS產生的能力。
    在抗氧化能力方面,ORAC (oxygen radical absorption capacity) 總抗氧化能力試驗中,發現結構衍生物七號及八號在20 ?嵱、40 ?嵱、80 ?嵱都有優於薑黃素的抗氧化能力。抑制AAPH誘導紅血球溶血試驗中,發現結構衍生物七號及八號在20 ?嵱、40 ?嵱、80 ?嵱對於抑制紅血球溶血的時間都較同濃度的薑黃素為長,顯示出較好的抗氧化活性。
    在動物實驗上,以D型半乳糖 (1.2 g/Kg bw/day) 的劑量誘導老化。透過被動迴避試驗評估其改善記憶能力的效果,在本篇研究中結構衍生物七號及八號沒有明顯的增加記憶恐懼的時間,故在行為學上沒有明顯的表現。在血清及組織的ORAC總抗氧化能力的實驗中,餵食結構衍生物七號及八號的組別,相較於實驗對照組在血清裡的ORAC值有顯著的提升,但在全腦組織中則沒有效果。而在丙二醛含量試驗中,餵食結構衍生物七號及八號的組別,在血清裡的丙二醛含量,相較於實驗對照組,有顯著的減少;而在全腦組織中只有在高濃度組 (10 mg/Kg bw) 顯示出其減少脂質過氧化的能力。
    而在抗發炎活性方面,利用LPS誘導RAW 264.7細胞株產生NO的方法,評估結構衍生物七號及八號抑制NO產生的能力。結構衍生物七號及八號在10 ?嵱下有顯著的減少NO產生,且皆較薑黃素為優。
    在本篇研究中,發現薑黃素結構衍生物七號及八號皆具有抗氧化及抗發炎的活性,但是在改善記憶功能的行為學研究上則沒有效果。

    Curcumin is the primary bioactive constituent of turmeric, which is an herbal medicine used in Asia for a long time. It has been shown to possess anti-inflammatory, antioxidant, and neuroprotection. In this study, curcumin and 23 different kinds of curcumin analogs were evaluated for antioxidant, anti-inflammatory and the ability to improve the learning and memory function in D-galactose-induced aging mice. According to the results of cell viability assay, analog 7 and 8 showed stronger neuroprotection and ROS inhibition activities against 6-OHDA, neurotoxic agent, in SH-SY5Y cell lines than curcumin under concentration of 10 μM. Besides, analogs 7 and 8 also showed better oxygen radical absorption capacity (ORAC) and the inhibitory effect of RBC hemolysis induced by AAPH than curcumin under concentration of 20, 40, 80 ?嵱 and were selected as test candidates for animal model.
    Taking 1.2g/Kg bw/day D-galatose subcutaneous injection on BALB/c male mice as the animal model for aging. By the step-through passive avoidance test, analog 7 and 8 didn’t improve the memory function at all. By ORAC and TBARS assay, analog 7 and 8 show the antioxidant activities through compare with the group D-galactose only on serum and whole brain. In anti-inflammatory activities, it was found that analog 7 and 8 could inhibit iNOS on whole brain and decrease NO production more than curcumin on RAW 264.7 induced inflammatory by LPS (1 ?慊/mL) .
    Description: 碩士
    委員-陳佩燁
    委員-蕭哲志
    指導教授-侯文琪
    Data Type: thesis
    Appears in Collections:[Graduate Institute of Pharmacognosy Science] Dissertation/Thesis

    Files in This Item:

    File Description SizeFormat
    index.html0KbHTML188View/Open


    All items in TMUIR are protected by copyright, with all rights reserved.


    著作權聲明 Copyright Notice
    • 本平台之數位內容為臺北醫學大學所收錄之機構典藏,包含體系內各式學術著作及學術產出。秉持開放取用的精神,提供使用者進行資料檢索、下載與取用,惟仍請適度、合理地於合法範圍內使用本平台之內容,以尊重著作權人之權益。商業上之利用,請先取得著作權人之授權。

      The digital content on this platform is part of the Taipei Medical University Institutional Repository, featuring various academic works and outputs from the institution. It offers free access to academic research and public education for non-commercial use. Please use the content appropriately and within legal boundaries to respect copyright owners' rights. For commercial use, please obtain prior authorization from the copyright owner.

    • 瀏覽或使用本平台,視同使用者已完全接受並瞭解聲明中所有規範、中華民國相關法規、一切國際網路規定及使用慣例,並不得為任何不法目的使用TMUIR。

      By utilising the platform, users are deemed to have fully accepted and understood all the regulations set out in the statement, relevant laws of the Republic of China, all international internet regulations, and usage conventions. Furthermore, users must not use TMUIR for any illegal purposes.

    • 本平台盡力防止侵害著作權人之權益。若發現本平台之數位內容有侵害著作權人權益情事者,煩請權利人通知本平台維護人員([email protected]),將立即採取移除該數位著作等補救措施。

      TMUIR is made to protect the interests of copyright owners. If you believe that any material on the website infringes copyright, please contact our staff([email protected]). We will remove the work from the repository.

    Back to Top
    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback