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硒多糖、亚砷酸钠对大鼠肝微粒体酶和GSH-Px等的影响
引用本文:程继忠,邬惠琼,海涛,宋瑞琨.硒多糖、亚砷酸钠对大鼠肝微粒体酶和GSH-Px等的影响[J].卫生毒理学杂志,1999,13(1):4-7.
作者姓名:程继忠  邬惠琼  海涛  宋瑞琨
作者单位:同济医科大学环境毒理学教研室,同济医科大学职业医学研究所
摘    要:研究了硒多糖、亚砷酸钠在体内、外对大鼠肝微粒体酶细胞色素P-450、b5、NAD(P)H-细胞色素C还原酶、谷胱甘肽硫转移酶(GST)的影响;并通过测定硒多糖、亚砷酸钠对肝谷胱甘肽过氧化物酶(GSH-Px)和脂质过氧化(LPO)的影响,探讨了硒、砷相互作用的机理。结果表明:连续7天腹腔注射0.2mg/kg硒多糖,细胞色素P-450、b5的含量、GST的活性降低(P<0.05);硒多糖明显诱导GSH-Px的活性,降低脂质过氧化,拮抗亚砷酸钠对LPO的作用。亚砷酸钠显著增强肝细胞脂质过氧化(P<0.05),对GSH-Px和肝微粒体酶无明显影响

关 键 词:硒多糖  亚砷酸钠  微粒体酶  谷胱甘肽过氧化物酶  脂质过氧化

Effects of selenium polysaccharide and sodium arsenite on rat liver mitocrosomal enzymes and glutathione peroxidase activity
Cheng Ji zhong\ Wu Hui qiong\ Hai Tao\ et al..Effects of selenium polysaccharide and sodium arsenite on rat liver mitocrosomal enzymes and glutathione peroxidase activity[J].Journal of Health Toxicology,1999,13(1):4-7.
Authors:Cheng Ji zhong\ Wu Hui qiong\ Hai Tao\
Abstract:The effects of selenium polysaccharide and sodium arsenite on the contents of microsomal cytochrome P450,b5 and activities of NAD(P)H cytochrome C reductase and glutathione S transferase in rat were studied in vivo and in vitro experiments.And the mechanism was also illuminated by determining their effects on the activity of glutathione peroxidase(GSH Px) and the lipid peroxidation.The results indicated:the contents of microsomal cytochrome P450 and b5 were decreased, activity of glutathione S transferase was inhibited after seleniunm polysaccharide administered by intraperitoneal injection daily for 7 days at a dose of 0 2mg/kg. The GSH Px activity was increased to 1 7 times of control group and the lipid peroxidation was decreased significantly by selenium polysaccharide( P <0 05).While sodium arsenite induced to increase the content of lipid peroxidation obviously( P <0 05) and had not appear to affect the liver cytosolic glutathione peroxidase and microsomal enzyme activities in vivo.These finding suggested that selenium polysaccharide could protect against lipid peroxidation induced by arsenic. \ \
Keywords:selenium polysaccharide  sodium arsenite  microsome engymes  glutathion peroxidase  lipid peroxidation
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