Peng A, Wang W H, Wang C X, Wang Z J, Rui H F, Wang W Z, Yang Z W
SKLEAC, Research Center for Eco-environmental Sciences, Chinese Academy of Sciences, Beijing 100085, P. R. China.
Environ Health Perspect. 1999 Apr;107(4):293-6. doi: 10.1289/ehp.99107293.
We conducted in vitro and in vivo assays in a selenium-deficient system to determine if organic matter (mainly fulvic acid; FA) is involved in a free radical mechanism of action for Kashin-Beck disease. Cartilage cell culture experiments indicated that the oxy or hydroxy functional groups in FA may interfere with the cell membrane and result in enhancement of lipid peroxidation. Experiments with rats demonstrated that toxicity from FA was reduced when the hydroxy group was blocked. Induction of lipid peroxidation by FA in liver and blood of rats was similar to that exhibited by acetyl phenyl hydrazine. FA accumulated in bone and cartilage, where selenium rarely concentrates. In addition, selenium supplementation in rats' drinking water inhibited the generation of oxy-free radicals in bone. We hypothesized that FA in drinking water is an etiological factor of Kashin-Beck disease and that the mechanism of action involves the oxy and hydroxy groups in FA for the generation of free radicals. Selenium was confirmed to be a preventive factor for Kashin-Beck disease.
我们在缺硒体系中进行了体外和体内试验,以确定有机物(主要是富里酸;FA)是否参与大骨节病的自由基作用机制。软骨细胞培养实验表明,FA中的氧基或羟基官能团可能干扰细胞膜并导致脂质过氧化增强。大鼠实验表明,当羟基被阻断时,FA的毒性降低。FA在大鼠肝脏和血液中诱导的脂质过氧化与乙酰苯肼所表现的相似。FA在骨骼和软骨中蓄积,而硒很少在这些部位聚集。此外,在大鼠饮用水中补充硒可抑制骨骼中氧自由基的产生。我们推测,饮用水中的FA是大骨节病的一个病因,其作用机制涉及FA中的氧基和羟基产生自由基。已证实硒是大骨节病的预防因素。