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作 者:尚雁君[1] 郭跃伟[2] 黄才国[1] 贾睿[2] 许强芝[1] 魏善建[1] 焦炳华[1] 张建荣[3]
机构地区:[1]第二军医大学基础医学部生物化学及分子生物学教研室,上海200433 [2]中国科学院上海药物研究所,上海201203 [3]第二军医大学长海医院实验诊断科,上海200433
出 处:《第二军医大学学报》2006年第1期25-27,共3页Academic Journal of Second Military Medical University
基 金:上海市中药现代化专项基金(05DZ19714).~~
摘 要:目的:本实验的目的是探讨中国南海海绵提取物renierol对黄嘌呤氧化酶的抑制作用及对小鼠高尿酸血症的影响。方法:从海绵中分离提取renierol成分,将20、40、60μg/ml renierol或1μg/ml阳性对照别嘌呤醇(1μg/ml),分别加入黄嘌呤溶液(50μmol/ml)和0.1 U/ml黄嘌呤氧化酶中,利用5 min超氧离子生成量来测定黄嘌呤氧化酶活性(NBT显色法)。再将20、40、60μg/ml renierol或100 U/ml阳性对照SOD加入25℃预热过的邻苯三酚,在波长420 nm处测定吸光值,观察renierol对自由基的直接清除作用。建立尿酸酶抑制剂氧嗪酸钾造成小鼠高尿酸血症模型,并给高、中、低剂量renierol组小鼠口服10、203、0 mg.kg-1renierol,别嘌呤醇组给药量为2 mg.kg-1,用全自动生化分析仪测定实验鼠的血清尿酸值,观察renierol体内降尿酸作用。结果:Renierol体外是黄嘌呤氧化酶的竞争性抑制剂,其IC50为1.36μg.ml-1,在体内也有明显的降尿酸作用。结论:Renierol通过抑制黄嘌呤氧化酶来降血尿酸。Objective:To study the inhibition of xanthine oxidase by renierol extracted from South China Sea sponge and study the influence of renierol on hyperuricemia in mice. Methods: After extracted from South China Sea sponge, renierol (20, 40, 60 μg/ml) was added to a system containing xanthine oxidase (0. 1 μ/ml) and xanthine (50 μmol/ml); allopurinol (1 μg/ml)was also addded to the system as positive control. The5 min-fomation of superoxide anions was used to determine the activity of xanthine oxidase (Nitro Blue Btetrazolium reduction). Renierol (20, 40, 60 μg/ml) was added to 25℃ pre heated pyrogallol autoxidation to observe its eliminating effect on free radicals through determining the absorbance rate at 420 nm wavelength. Potassium oxonate, a uricaseinhibitor, was used to induce hyperuricemia in mice and the mice were then treated withoral renierol (10, 20, 30 mg·kg^-1) orallopurinol (2 mg/kg) as positive control. The decrease of serum uric acid induced byrenierol was determined by automatic biochemical analyzer. Results: Renierol was demonstrated to be a competitive inhibitor of xanthine oxidase in vitru, with its IC〉 value being 1.36μg·ml^-1. It also decreased uric acid in vivo. Conclusion: Renierol can decrease serum uric acid through inhibiting the xanthine oxidase .
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