English  |  正體中文  |  简体中文  |  全文筆數/總筆數 : 45384/58560 (78%)
造訪人次 : 2509030      線上人數 : 178
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/987654321/5062


    題名: 銀杏、人參、五味子萃取物複方對四氯化碳誘發肝傷害老鼠肝功能的影響
    Effects of Ginkgo biloba, Panax ginseng, and Schizandra chinensis extract on the functions of damaged liver induced by carbon tetrachlorede
    作者: 張馨方
    Hsin-Fang Chang
    貢獻者: 保健營養學研究所
    關鍵詞: 銀杏
    人參
    五味子
    肝傷害
    Ginkgo biloba
    Panax ginseng
    Schizandra chinensis
    liver damage
    日期: 2005
    上傳時間: 2009-09-10 18:03:02 (UTC+8)
    摘要: 本研究是探討銀杏(Ginkgo biloba)、人參(Panax ginseng)、五味子(Schizandra chinensis)萃取物複方,對CCl4誘發肝傷害老鼠肝功能,抗氧化力及脂質代謝的影響。Sprague-Dawley老鼠以隨機方式分為正常組、CCl4組、CCl4+sliymarin (200 mg/kg/day)組、CCl4+一倍劑量(150 mg/kg/day)組及CCl4+五倍劑量(750 mg/kg/day)組,實驗為期六週。結果顯示,第四週時CCl4組血漿GOT、GPT值顯著高於正常組,CCl4+sliymarin組和CCl4+一倍劑量組之GOT有較CCl4組顯著下降的情形,CCl4+一倍劑量組之GPT值也較CCl4組顯著下降。肝臟抗氧化方面,CCl4組之SOD活性顯著低於正常組,其餘三組與正常組間則無顯著差異,而CCl4+五倍劑量組之catalase活性顯著高於CCl4組,肝臟總抗氧化狀態,CCl4組顯著低於其他四組,CCl4組肝臟中脂質過氧化物MDA含量顯著高於正常組,CCl4+一倍劑量組及CCl4+五倍劑量組則與正常組間無顯著差異,病理切片發現,CCl4+一倍劑量組及CCl4+五倍劑量組肝纖維化有較CCl4組改善。CCl4+一倍劑量組及CCl4+五倍劑量組血漿總膽固醇含量顯著低於CCl4組。由結果推測,此複方可改善因CCl4誘發肝傷害老鼠之肝臟抗氧化能力,並延緩肝纖維化之發生。
    This study investigated the effects of herbal cocktail (Ginkgo biloba, Panax ginseng, and Schizandra chinensis extract) on hepatic functions, antioxidation and lipid metabolism in rats with CCl4-induced liver damage. Sprague-Dawley rats were randomly divided into control, CCl4, CCl4+silymarin(200 mg/kg), CCl4+1herbal extract cocktail(HEC; 150 mg/kg), and CCl4+5HEC(750 mg/kg) groups. The experimental period was 6 weeks. The results showed that the CCl4 group significantly increased plasma GOT and GPT activities at week 4 compared with the control group. However, the 1HEC group significantly decreased plasma GOT and GPT activities at week 4 compared with the CCl4 group. Hepatic SOD activity in the CCl4 group showed significantly lower than that in the control group. The activity of SOD in other three CCl4 groups was not significantly different compared with that in the control group. Hepatic catalase activity in the CCl4+5HEC group showed significantly higher than that in the CCl4 group. The total antioxidant status in the CCl4 group significantly lower than that in other groups. Additionally, hepatic MDA concentration in the CCl4 group was significantly higher than that in the control group. However, MDA concentration in both CCl4+1HEC and CCl4+5HEC groups’ was not significantly different compared with that in the control group. The pathologic results showed that liver fibrosis was ameliorated in the CCl4+1HEC and CCl4+5HEC groups compared with that in the CCl4 group. In addition, both CCl4+1HEC and 5HEC groups significantly decreased plasma total cholesterol compared with the CCl4 group. These results suggest that HEC can improve hepatic antioxidative capacity and decrease liver fibrosis occurring in rats with CCl4-induced liver damage.
    資料類型: thesis
    顯示於類別:[保健營養學系暨研究所] 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.doc29KbMicrosoft Word118檢視/開啟
    摘要.pdf60KbAdobe PDF151檢視/開啟
    摘要.ppt118KbMicrosoft Powerpoint235檢視/開啟
    摘要.ps316KbPostscript92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