硒
谷胱甘肽过氧化物酶
化学
谷胱甘肽
硫氧还蛋白还原酶
抗氧化剂
GPX1型
谷胱甘肽还原酶
硫氧还蛋白
生物化学
GPX3型
氧化应激
酶
有机化学
作者
Jinsong Zhang,Xue‐Yun Gao,Lide Zhang,Yongping Bao
出处
期刊:Biofactors
[Wiley]
日期:2001-01-01
卷期号:15 (1): 27-38
被引量:501
标识
DOI:10.1002/biof.5520150103
摘要
Abstract A novel selenium form, nano red elemental selenium (Nano‐Se) was prepared by adding bovine serum albumin to the redox system of selenite and glutathione. Nano‐Se has a 7‐fold lower acute toxicity than sodium selenite in mice (LD 50 113 and 15 mg Se/kg body weight respectively). In Se‐deficient rat, both Nano‐Se and selenite can increase tissue selenium and GPx activity. The biological activities of Nano‐Se and selenite were compared in terms of cell proliferation, enzyme induction and protection against free racial‐mediated damage in human hepatoma HepG2 cells. Nano‐Se and selenite are similarly cell growth inhibited and stimulated synthesis of glutathione peroxidase (GPx), phospholipid hydroperoxide glutathione peroxidase (PHGPx) and thioredoxin reductase (TR). When HepG2 cells were co‐treated with selenium and glutathione, Nano‐Se showed less pro‐oxidative effects than selenite, as measured by cell growth. These results demonstrate that Nano‐Se has a similar bioavailability in the rat and antioxidant effects on cells.
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