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作 者:吴迪[1] 周诗珈 李霞[1,2] 秦艳杰[1] 白丽雯[1] 王文文[1] WU Di ZHOU Shi-jia LI Xia QIN Yan -jie BAI Li-w e n WANG Wen -wen(Key Laboratory of Marine Bio-resources Restoration and Habitat Reparation in Liaoning Province,Dalian Ocean Lniversity,Dalian 116023,China Key Laboratory of Mariculture & Stock Enhancement in North China’s Sea,Ministry of Agriculture,Dalian Ocean Lniversity,Dalian 116023, China)
机构地区:[1]大连海洋大学辽宁省海洋生物资源恢复与生境修复重点实验室,辽宁大连116023 [2]大连海洋大学农业部北方海水增养殖重点实验室,辽宁大连116023
出 处:《大连海洋大学学报》2016年第6期646-650,共5页Journal of Dalian Ocean University
基 金:国家自然科学基金资助项目(31272650)
摘 要:为探究重铬酸钾的毒性机制,建立适合监测铬污染的体外检测系统,以体外培养的泥鳅Misgurnus anguillicaudatus鳍细胞系(DIMF)为试验材料,研究了重铬酸钾的毒性效应。结果表明:通过噻唑蓝(MTT)比色法测定重铬酸钾染毒后细胞的24 h半致死浓度为(25.3±1.2)滋mol/L;暴露在浓度为0~30滋mol/L的重铬酸钾中,细胞超氧化物歧化酶(SOD)活性随着染毒浓度的增加而增大;谷胱甘肽超氧化物酶(GSH-Px)在重铬酸钾浓度为0~20滋mol/L时活性升高,当染毒浓度为30 mol/L时,活力开始下降;谷胱甘肽S-转移酶(GST)活性则随重铬酸钾浓度的升高而降低;微核试验显示,DIMF微核率随染毒浓度的增加呈先升高后降低的趋势,其中最大微核率为0.733%;实时定量PCR结果显示,对照组的金属硫蛋白(MT)基因表达量很低,经重铬酸钾诱导后MT基因表达量显著升高(P〈0.01)。研究表明,重铬酸钾可对细胞的酶系统和遗传物质造成一定的损伤。Loach Misgurnus anguillicaudatus fin cell line ( D I M F ) was used to assess toxicity of potassium dichro-mate in vitro to study toxicity mechanism of potassium dichromate and establish suitable for chrome pollution detec-tion system. The results showed that the median lethal concentration ( LC50) was (25. 3 ± 1 . 2 )μmo l / L in D I M F exposed to potassium dichromate for 24 h measured by thiazole blue ( M TT ) method. T he activities of superoxide dismutase ( SOD ) in DIMF were increased with the increase in concentration within potassium dichromate concen-tration of 0-30 滋 mo^L and the activities of glutathione peroxidase ( G S H -P x ) were increased at 0-20 μmol/ L po-tassium dichromate, and then decreased at concentration of 30 μmol/L,with gradual decrease in glutathione S transferase( GST ) activity. Micronucleus test revealed that the rate of micronucleus was increased first and then de-creased with the increase in potassium dichromate concentration,with the m a x i m u m micronucleus rate of 0.733%. Real-time PCR showed that metallothionein (MT ) gene expression quantity was very low in control group,and in-creased significantly due to the induction by potassium dichromate( P〈0. 01). T he findings indicate that potassium bichromate can damage enzyme system and genetic materials in cells.
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