Du Jin-Liang, Cao Li-Ping, Liu Ying-Juan, Jia Rui, Yin Guo-Jun
Key Laboratory of Freshwater Fisheries and Germplasm Resources Utilization, Ministry of Agriculture, Freshwater Fisheries Research Center, Chinese Academy of Fishery Sciences, Wuxi, 214081, China.
International Joint Research Laboratory for Fish Immunopharmacology, Freshwater Fisheries Research Center, Chinese Academy of Fishery Sciences, Wuxi, 214081, China.
Bull Environ Contam Toxicol. 2016 Jan;96(1):55-61. doi: 10.1007/s00128-015-1683-5. Epub 2015 Oct 27.
The aim of this study was to establish a model for the study of liver injury induced by 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) in Jian carp using precision-cut liver slices (PCLS). PCLS were treated with TCDD at concentrations of 0, 0.05, 0.1, 0.3, and 0.6 μg/L for 6 h, followed by collection of the culture supernatant and PCLS for analysis. Several biochemical indices were analyzed, including glutamic pyruvic transaminase (GPT), glutamic oxaloacetic transaminase (GOT), lactate dehydrogenase (LDH), superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), and malondialdehyde (MDA). Expression of mRNA was also estimated for cytochrome P4501A (CYP1A), aryl hydrocarbon receptor2 (AhR2), and aryl hydrocarbon receptor nuclear translocator2 (ARNT2). Results showed that some significant effects (p < 0.05) in MDA, GSH-Px and PCLS viability were observed at a TCDD concentration as low as 0.05 µg/L, and the observed effects increased with exposure concentration. Following exposure to TCDD for 6 h at a concentration of 0.3 μg/L, significant increases (p < 0.01) in the content of GPT, GOT, MDA, and LDH were observed, while SOD activity, GSH-Px activity, and PCLS viability were decreased (p < 0.01 or p < 0.05). Exposure to 0.3 μg/L TCDD also resulted in increased expression of mRNA for CYP1A, AhR2, and ARNT2. Overall, these results provide evidence of TCDD-induced liver injury and oxidative stress in Jian carp. These results also support the use of PCLS as an in vitro model for the evaluation of hepatotoxicity in Jian carp.
本研究的目的是建立一个使用精密肝切片(PCLS)研究2,3,7,8-四氯二苯并对二恶英(TCDD)诱导建鲤肝损伤的模型。将PCLS分别用浓度为0、0.05、0.1、0.3和0.6μg/L的TCDD处理6小时,随后收集培养上清液和PCLS进行分析。分析了几种生化指标,包括谷丙转氨酶(GPT)、谷草转氨酶(GOT)、乳酸脱氢酶(LDH)、超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GSH-Px)和丙二醛(MDA)。还评估了细胞色素P4501A(CYP1A)、芳烃受体2(AhR2)和芳烃受体核转运蛋白2(ARNT2)的mRNA表达。结果表明,在TCDD浓度低至0.05μg/L时,MDA、GSH-Px和PCLS活力出现了一些显著影响(p<0.05),且观察到的影响随暴露浓度增加而增大。在0.3μg/L浓度下暴露于TCDD 6小时后,观察到GPT、GOT、MDA和LDH含量显著增加(p<0.01),而SOD活性、GSH-Px活性和PCLS活力降低(p<0.01或p<0.05)。暴露于0.3μg/L TCDD还导致CYP1A、AhR2和ARNT2的mRNA表达增加。总体而言,这些结果提供了TCDD诱导建鲤肝损伤和氧化应激的证据。这些结果也支持将PCLS用作评估建鲤肝毒性的体外模型。