Repository logo
  • English
  • 中文
  • Log In
    New user? Click here to register.Have you forgotten your password?
Repository logo
    Communities & Collections
    Research Outputs
    Fundings & Projects
    People
    Organizations
    Statistics
  • English
  • 中文
  • Log In
    New user? Click here to register.Have you forgotten your password?
  1. Home
  2. .TMU Publications / 北醫出版品(教師升等著作 / 教學實踐 / 學位論文)
  3. .博碩士學位論文
  4. .95學年度
  5. 厚朴酚對於尿壓素誘發心臟纖維細胞增生的作用
 
  • Details
Options

厚朴酚對於尿壓素誘發心臟纖維細胞增生的作用

Other Title
Effect of magnolol on urotensin II-induced cardiac fibroblast proliferation
Type
thesis
Date Issued
2006-05-23
Author(s)
陳燕玲
Advisor
洪傳岳
Subjects
系所名稱:醫學科學研究所
Description
學位別:碩士
語文別:中文
指導教授:洪傳岳
共同指導教授:劉如濟
口試委員:陳錦澤;羅時鴻;施能朗
中文關鍵字:厚朴酚;尿壓素;活性氧族群;胞外訊息調節激酶內皮素;心臟纖維細胞增生
Abstract
厚朴酚(Magnolol)是從中國草本植物厚朴所萃取出來的一種物質,具有抗氧化、抗血栓形成、抗焦慮、抗發炎、血管放鬆等藥理特性。近期的研究也發現會造成許多不同癌細胞株凋亡的作用。在心血管方面,厚朴酚會有抑制血管平滑肌細胞增生的作用,然而對於心臟纖維細胞的作用及相關的細胞分子機制都還不是很清楚。尿壓素(Urotensin-Ⅱ; U-Ⅱ)為目前已知具有強力促進血管收縮作用的內生性物質,而且與高血壓及心血管疾病如冠狀動脈硬化及心臟衰竭有密切關聯,動物實驗的結果顯示尿壓素對於心臟重塑及纖維化過程的發生會有促進的作用 (Lapp et al.,2004)。本研究目的即在於以培養的離體心臟纖維細胞,觀察尿壓素對於心臟纖維細胞的作用,並進一步探討厚朴酚是否會抑制由尿壓素所誘發心臟纖維細胞的作用,據以了解厚朴酚在尿壓素所誘發心臟纖維細胞作用的相關細胞分子機轉。
於培養的初生鼠心臟纖維細胞給予不同濃度尿壓素的處理後,發現尿壓素會促進心臟纖維細胞的增生,以及增加內皮素蛋白質的表現。至於細胞內的作用機制,尿壓素對細胞內活性氧族群以及胞外訊息調節激酶活性皆會有增加的作用。進一步觀察厚朴酚對於心臟纖維細胞的作用,單獨厚朴酚的處理,在30µM濃度以上,會造成細胞的毒性作用。厚朴酚在10µM濃度內,對於尿壓素增加細胞內活性氧族群、胞外訊息調節激酶活性、內皮素蛋白質表現以及細胞增生則會有抑制作用。
本研究結果發現尿壓素具有增加心臟纖維細胞內活性氧族群的產生、胞外訊息調節激酶活性、內皮素蛋白質表現,以及促進細胞增生的作用。尿壓素誘發心臟纖維細胞增生以及相關細胞內的作用則會被厚朴酚抑制,結果顯示厚朴酚或許將有助於尿壓素所誘發相關心臟纖維化之治療運用。
URI
https://203.71.86.71/handle/123456789/12110
https://hdl.handle.net/11296/u9474p
File(s)
No Thumbnail Available
Name

C0183246.pdf

Size

7.79 MB

Format

Adobe PDF

Checksum

(MD5):170d53213aa4ebdf18036c0340d4094b

Copyright Notice

● 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. Users must not use TMUIR for any illegal purposes.

● By utilising the platform, users are deemed to have fully accepted and understood all the regulations set out in this statement, relevant laws of the Republic of China, all international internet regulations, and usage conventions.

● TMUIR is committed to protecting the interests of copyright owners. If you believe that any material on this website infringes copyright, please contact our staff at libirtmu@gmail.com, and we will remove the work from the repository.

Built with DSpace-CRIS software - Extension maintained and optimized by 4Science

  • Cookie settings
  • Privacy policy
  • End User Agreement
  • Send Feedback