The effects of high levels of vitamin E supplementation on immune reponses and disease progress in autoimmune-prone MRL/lpr mice

碩士 === 國立臺灣大學 === 農業化學系研究所 === 86 === The MRL/lpr mice develop a syndrome that resembles human systemic lupus erythematosus ( SLE ), including production of autoantibodies and formation of immune complexes. They have a strikingly short life span and die a...

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Bibliographic Details
Main Authors: Fang, Su-Chi, 方素琦
Other Authors: Bi-Fong Lin
Format: Others
Language:zh-TW
Published: 1998
Online Access:http://ndltd.ncl.edu.tw/handle/19942765694751212340
Description
Summary:碩士 === 國立臺灣大學 === 農業化學系研究所 === 86 === The MRL/lpr mice develop a syndrome that resembles human systemic lupus erythematosus ( SLE ), including production of autoantibodies and formation of immune complexes. They have a strikingly short life span and die at the age of 6~8 months secondary to renal failure. The purpose of this study was to investigate the effects of high levels of vitamin E supplementation on the autoimmune disease courses. Ninety weanling MRL/lpr female mice were randomly divided into three groups and respectively fed on an AIN-76 diet containing 5% fresh soybean oil ( Control ), control diet supplemented with vitamin E at 10 times levels of AIN-76 ( E10 ), or 20 times levels ( E20 ).After 14 weeks, half of the mice were killed for in vitro experiments at 5 months of age. The results showed that the relative weights of spleen and kidney were reduced in E10 and E20 groups. Supplementation with all-rac--tocopheryl acetate elevated the -tocopherol content and reduced TBARS in liver and kidney. With respect to the antioxidant enzyme activities, the hepatic SOD and GSH-Px activity were significantly ( p<0.05 ) higher in E20 group and the renal SOD activity was significantly higher in E10 group. The E10 and E20 groups had lower IL-6 and PGE2 secreted from peritoneal cells than the control group. PGE2 production by spleen cells was also reduced in E10 and E20 groups. But there were no effects on TNF-、IL-6 and IL-10 production. In conclusion, vitamin E supplementation decreases the oxidative stress and the PGE2 production from splenocytes and peritoneal macrophage, but it neither reduce the autoantibody production nor prolong the life span through the Th1、Th2 cells regulation in MRL/lpr mice.