Glutathione S-transferase and UDP-glucuronyltransferase activity in primary cultures of rainbow trout gill epithelial cells

Maria Sandbacka, Boris Isomaa
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引用次数: 10

Abstract

The objective of this study was to characterize rainbow trout (Oncorhynchus mykiss) gill epithelial cells in primary culture by evaluating their ability to maintain glutathione and glucuronide conjugating enzymes. The activity and inducibility of the phase II enzymes was investigated as a function of culture time. Glutathione S-transferase (GST) and UDP-glucuronyltransferase (UDPGT) enzyme activities were measured in freshly isolated cells and in cells cultured for 7 and 12 days. GST activity, determined with 1-chloro-2,4-dinitrobenzene, decreased gradually to 72% after 7 days and to 38% after 12 days in culture compared with freshly isolated cells. There was no significant difference between UDPGT activities in freshly isolated cells compared with cells cultured up to 12 days although a transient decrease in activity was observed at day 7. In vitro induction of the enzymes was studied using β-naphtoflavone (BNF) and 3-methylcholanthrene (3-MC) as inducers. GST activity increased 2-fold after exposure to BNF and 1.5-fold after 3-MC exposure for 48 h in 7 days old cultures. No induction was observed in 12 days old cultures. UDPGT activity was not induced either at day 7 or 12.

虹鳟鱼鳃上皮细胞谷胱甘肽s -转移酶和udp -葡萄糖醛基转移酶活性研究
本研究的目的是通过评估虹鳟鱼(Oncorhynchus mykiss)原代培养中鳃上皮细胞维持谷胱甘肽和葡萄糖醛酸盐偶联酶的能力来表征虹鳟鱼(Oncorhynchus mykiss)。研究了II期酶的活性和诱导性随培养时间的变化。在新鲜分离的细胞和培养7、12 d的细胞中测定谷胱甘肽s转移酶(GST)和udp -葡萄糖醛基转移酶(UDPGT)酶活性。用1-氯-2,4-二硝基苯测定GST活性,与新鲜分离的细胞相比,培养7天后逐渐下降到72%,12天后下降到38%。与培养12天的细胞相比,新分离的细胞中的UDPGT活性没有显著差异,尽管在第7天观察到活性短暂下降。以β-萘黄酮(BNF)和3-甲基胆蒽(3-MC)为诱导剂,研究了这些酶的体外诱导作用。在7天大的培养物中,暴露于BNF 48小时后,GST活性增加了2倍,暴露于3-MC 48小时后,GST活性增加了1.5倍。在12天龄的培养物中未观察到诱导。第7天和第12天均未诱导UDPGT活性。
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