English  |  正體中文  |  简体中文  |  全文筆數/總筆數 : 45422/58598 (78%)
造訪人次 : 2521787      線上人數 : 181
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜尋範圍 查詢小技巧:
  • 您可在西文檢索詞彙前後加上"雙引號",以獲取較精準的檢索結果
  • 若欲以作者姓名搜尋,建議至進階搜尋限定作者欄位,可獲得較完整資料
  • 進階搜尋
    請使用永久網址來引用或連結此文件: http://libir.tmu.edu.tw/handle/987654321/6736


    題名: Quercetin及其衍生物抑制RAW 264.7細胞因LPS刺激而產生的NO與其結構-活性關係
    Inhibitory Effects of Quercetin and Its Derivatives on LPS-Induced NO Production in RAW 264.7 Cells and Their Structure-Activity Relationships
    作者: 陳姿廷
    Tzu-Ting Chen
    貢獻者: 藥理學研究所
    關鍵詞: 一氧化氮
    誘導型一氧化氮酶
    類黃鹼素
    老鼠巨噬細胞
    脂多醣體
    Nitric oxide
    inducible nitric oxide synthase
    quercetin
    RAW 264.7
    lipopolysaccharides
    日期: 2004
    上傳時間: 2009-09-11 17:32:49 (UTC+8)
    摘要: Quercetin及其衍生物對Phosphodiesterase(PDE)isozyme分別有不同程度的抑制作用,特別Quercetin對PDE 4/3有選擇性及競爭性的抑制作用,並對氣喘治療具有潛力,因此它們應有抗發炎的作用,但很少有此報告,特別是它們抗發炎的構造-活性之關係更是缺如。我們擬將RAW 264.7細胞以LPS(100 ng/ml)刺激RAW 264.7細胞使產生NO,NO含量的測定採用Griess reaction。根據結果顯示Quercetin抑制NO產生的能力最強,這可能因C3,C5,C7,C3’,C4’位上都有-OH group,因此很容易與其標的蛋白質形成氫鍵,因這些OH group若被-CH3取代越多,其抑制NO產生的能力就越弱,但以4個OH group被取代為最,如QTME就完全沒有作用(IC50>100μM)。此種抑制NO產生的IC50值與抑制iNOS蛋白質表現的IC50值非常吻合,顯示抑制NO產生主要來自於iNOS蛋白質受抑制,因以cell-free system研究SNP產生的NO或SNP產生NO後被捕抓的情形,顯示這些Quercetin及其衍生物並無作用。此構造-活性關係之探討,有助於合成有用的抗發炎藥物。
    Quercetin and its derivatives have been reported to inhibit phosphodiesterase(PDE)isozyme in various extent. Especially, quercetin selectively and competitively inhibits PDE 4/3, and has potential in the treatment of asthma. Therefore, they have anti-inflammatory effect. However, there are few reports about that, especially the relationships between structure and activity is little known. We plan to determine NO production according to the method of Griess in LPS(100 ng/ml)—activated RAW 264.7 cells. In the present results, quercetin and its derivatives except QTME, concentration-dependently inhibited the NO production. It revealed quercetin the most potently inhibited the NO production with an IC50 value of 2.17 ± 0.06μM. The IC50 values of other derivatives are presented in Table 2, Quercetin had the most potency among these compounds, suggesting its C3-, C5-, C7-, C3’- and C4’-hydroxyl groups may bind to the binding sites of target proteins. It seems the more hydroxyl group are substituted by methoxy groups the more potency decreases. However the number of substitution maximally occurs at four. For example, QTME almost had no effect(IC50 > 100μM)on the NO production. The IC50 values of quercetin and its derivativeson NO production were similar to those of iNOS protein expression, suggesting the NO production is mainly due to iNOS protein expression, because in cell-free system, they had no effect on SNP-induced NO production and NO release. It may be helpful to syntheaize useful anti-inflammatory drugs, after the study of relationships between their structures and activities.
    資料類型: thesis
    顯示於類別:[藥學系] 博碩士論文

    文件中的檔案:

    檔案 描述 大小格式瀏覽次數
    摘要.doc28KbMicrosoft Word141檢視/開啟
    摘要.pdf743KbAdobe PDF237檢視/開啟
    摘要.ppt111KbMicrosoft Powerpoint187檢視/開啟
    摘要.ps442KbPostscript67檢視/開啟


    在TMUIR中所有的資料項目都受到原著作權保護.

    TAIR相關文章

    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 ©   - 回饋