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. .98學年度
  5. 正常光暗周期下大鼠海馬迴中誘導型一氧化氮生成酶之基因表達與機制研究
 
  • Details
Options

正常光暗周期下大鼠海馬迴中誘導型一氧化氮生成酶之基因表達與機制研究

Other Title
The Expression and Mechanism of Inducible Nitric Oxide Synthase in Hippocampus of Rats under Normal Light-Dark Cycle
Type
thesis
Date Issued
2010-06-30
Author(s)
謝家瑜
Advisor
王家儀
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:王家儀
共同指導教授:李怡萱
口試委員:胡朝榮;呂思潔;宋俊松
中文關鍵字:光暗周期;海馬迴;誘導型一氧化氮生成酶cAMP response element binding protein (CREB)
Abstract
摘要
「日變節律」是動物經由光照刺激透過視交叉上核,將體內每日的生理週期與外界環境,約略以24小時的節律作同步化規律性循環。研究指出CREB及nNOS在視交叉上核中有節律性表達,而當日變節律受到干擾則會造成iNOS增加,然而在目前仍未知正常光暗周期下iNOS的表達變化。
為了解iNOS在日變節律受到干擾後大量表現的機轉,首先探討iNOS在日變節律中的節律變化,12小時光照-12小時黑暗及24小時全暗的條件下,以RT-PCR探測大鼠大腦皮質、海馬迴及血中iNOS之表達,以及西方墨點分析法觀察海馬迴iNOS及phospho-CREB蛋白質量的變化,並更進一步以染色質免疫沉澱分析法觀察轉錄因子phospho-CREB與iNOS啟動子結合的現象。結果發現海馬迴iNOS基因表達高峰期出現在ZT 6及ZT 22;海馬迴iNOS 蛋白質則呈現節律性的表達,而其高峰期出現在ZT 18出現,且發現iNOS蛋白質量於iNOS mRNA表達增加的時間點-ZT 22之後有逐漸增加的現象,於ZT 8達到高峰;再者調控日變節律基因表達之轉錄因子的實驗結果顯示,磷酸化態的CREB蛋白質量於黑暗期比光亮期多,其高峰則出現在ZT 18及ZT 22,而轉換到光亮期後,CREB磷酸化態蛋白質則呈現低點;而由在染色質免疫沉澱分析
法的實驗中也證實於ZT18,磷酸化態CREB會結合至iNOS啟動子上;再者我們發現血中iNOS基因表達與海馬迴iNOS基因表達呈現同步的現象。
綜合以上之研究顯示海馬迴iNOS在正常光暗周期中存在日變節律,且會透過CREB的磷酸化調節iNOS基因的表達。
URI
https://203.71.86.71/handle/123456789/13287

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