S-腺核苷同半胱胺酸對RAW264.7巨噬細胞在LPS誘發免疫反應下的機制探討

CNU IR > College of Sustainable Environment and Recreation > Dept. of Recreation and Health-Care Management > Chna Project > Item 310902800/9931

jsp.display-item.identifier=請使用永久網址來引用或連結此文件: https://ir.cnu.edu.tw/handle/310902800/9931

题名:	S-腺核苷同半胱胺酸對RAW264.7巨噬細胞在LPS誘發免疫反應下的機制探討
作者:	蔡新茂
贡献者:	休閒保健管理系
日期:	2008
上传时间:	2009-02-20 11:44:22 (UTC+8)
出版者:	台南縣：嘉南藥理科技大學休閒保健管理系
摘要:	The limited research has been performed regarding the s-adenosylhomocysteine (SAH) or homocysteine (Hcy)-evoked cell damage in hepatic and neuronal cells. In this study we assessed effects of SAH or Hcy in hepatic and neuronal cells on cell cytotoxicity and DNA damage, and attempted to find the underlying mechanism. Cell cytotoxicity and DNA damage were evaluated in murine hepatic cells (BNL CL.2 cell line) and microglia cells (BV-2 cell line) with SAH or Hcy treatment for 48 hours. The influences of SAH or Hcy on lipid peroxidation and DNA methylation were also measured in both cell lines. SAH (5-20 M) or Hcy (1-5 mM) dose dependently inhibited cell cytotoxicity and enhanced DNA damage in both types of cells. Furthermore, SAH treatment markedly increased intracellular SAH levels and DNA hypomethylation, the effect of SAH was much stronger than that of Hcy. The findings were also obtained that Hcy significantly induced lipid peroxidation, but not SAH. The present results show that SAH might cause cellular DNA damage in hepatic and microglia cells by DNA hypomethylation, further resulting in irreversible DNA damage and decrement of cell cytotoxicity. Additionally, higher Hcy could induce cellular DNA damage through increased lipid peroxidation and DNA hypomethylation. We suggest that SAH is more informative to cell damage than that of Hcy in hepatic and microglia cells.
關聯:	計畫編號：CN9737
显示于类别:	[Dept. of Recreation and Health-Care Management] Chna Project

文件中的档案:

档案	描述	大小	格式	浏览次数
97CN9737.pdf		186Kb	Adobe PDF	1134	检视/开启

在CNU IR中所有的数据项都受到原著作权保护.

TAIR相关文章

数据加载中.....