Yang Z L, Jia X A, Zhao J Y, Li T L, Xu G L
Department of Biochemistry, Xi'an Medical University, Shaanix, P.R. of China.
J Trace Elem Electrolytes Health Dis. 1992 Sep;6(3):161-7.
Six groups of weanling rats were fed a low-selenium based diet containing less than 0.01 mg/kg of Se in the diet or the basal diet supplemented with five levels of selenium as selenite (0.1, 0.2, 0.3, 0.4 and 0.5 mg/kg) for at least 16 to 18 weeks. For determination of the effect of selenium on ribonucleic acid (RNA) synthesis in rat liver, rats of each dietary group were injected with a single dose of (5-3H)-uridine, and 3 hours later their livers were removed and subjected to cell fractionation. The radioactivities in the nuclear and cytoplasmic RNA were taken as a measure of the RNA synthesis rate. With selenium supplementation between 0.2 and 0.5 mg/kg diet, the radioactivities, amounts of RNA, as well as RNA/DNA ratios in both nuclear and cytoplasmic fractions of rat liver all increased significantly. In addition, at similar levels of selenium supplementation, statistically significant increments of glutathione peroxidase (GSH-Px) activity and reductions in lipid peroxide in liver were also observed. For assessment of RNA degradation, activities of ribonucleases (RNase) and RNase inhibitor in rats fed the low-selenium diet or a selenium-supplemented diet were determined. The activities of acid RNase and both free and latent alkaline RNase in liver homogenate were not affected by selenium deficiency; however, the level of RNase inhibitor present in the supernatant fraction increased significantly with selenium supplementation at 0.2 mg/kg diet.(ABSTRACT TRUNCATED AT 250 WORDS)
将六组断乳大鼠分别喂食低硒基础日粮(日粮中硒含量低于0.01毫克/千克)或添加五种亚硒酸钠水平(0.1、0.2、0.3、0.4和0.5毫克/千克)的基础日粮,持续至少16至18周。为了测定硒对大鼠肝脏核糖核酸(RNA)合成的影响,给每个日粮组的大鼠注射单剂量的(5-3H)-尿苷,3小时后取出肝脏并进行细胞分级分离。细胞核和细胞质RNA中的放射性被用作RNA合成速率的指标。日粮中硒添加量在0.2至0.5毫克/千克之间时,大鼠肝脏细胞核和细胞质部分的放射性、RNA含量以及RNA/DNA比率均显著增加。此外,在相似的硒添加水平下,还观察到肝脏中谷胱甘肽过氧化物酶(GSH-Px)活性有统计学意义的增加以及脂质过氧化物减少。为了评估RNA降解,测定了喂食低硒日粮或硒补充日粮大鼠体内核糖核酸酶(RNase)和RNase抑制剂的活性。肝脏匀浆中酸性RNase以及游离和潜在碱性RNase的活性不受硒缺乏的影响;然而,当日粮中硒添加量为0.2毫克/千克时,上清液部分中RNase抑制剂的水平随硒补充而显著增加。(摘要截选至250字)