Ren Xianyun, Wang Zhuqing, Gao Baoquan, Liu Ping, Li Jian
Key Laboratory for Sustainable Utilization of Marine Fisheries Resources, Ministry of Agriculture, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao, PR China; Function Laboratory for Marine Fisheries Science and Food Production Processes, Qingdao National Laboratory for Marine Science and Technology, Qingdao, PR China.
Key Laboratory for Sustainable Utilization of Marine Fisheries Resources, Ministry of Agriculture, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao, PR China; Function Laboratory for Marine Fisheries Science and Food Production Processes, Qingdao National Laboratory for Marine Science and Technology, Qingdao, PR China; College of Fisheries and Life Science, Dalian Ocean University, Dalian, PR China.
Ecotoxicol Environ Saf. 2017 Sep;143:6-11. doi: 10.1016/j.ecoenv.2017.05.003. Epub 2017 May 6.
Florfenicol (FLR) is the most commonly used antibacterial agent in aquaculture because of its wide spectrum of activity and few side-effects. We characterized the toxicokinetics of FLR in the swimming crab (Portunus trituberculatus) after intravenous (IV) dosing (20, 40 and 80mg/kg). The results showed that FLR significantly suppressed the antioxidant system of the hepatopancreas. FLR induced transcriptional expression of phase I and phase II detoxification genes (CYP3 and GST, respectively) in a dose- and clearance time-dependent manner and altered the expression of their corresponding enzymes (erythromycin N-demethylase and glutathione S-transferase, respectively). Moreover, FLR induced the transcription of ATP-binding cassette (ABC) transporter subfamily B (ABCB) and subfamily G (ABCG), although ABCG transcription was not induced by FLR at 20mg/kg. Additionally, higher FLR doses caused significant biomolecule damage during the first 48h after delivery. This study will provide an improved understanding of the exact mechanism underlying toxicity in aquatic organisms.
氟苯尼考(FLR)因其抗菌谱广、副作用少,是水产养殖中最常用的抗菌剂。我们对静脉注射(20、40和80mg/kg)后三疣梭子蟹体内氟苯尼考的毒代动力学进行了表征。结果表明,氟苯尼考显著抑制了肝胰腺的抗氧化系统。氟苯尼考以剂量和清除时间依赖性方式诱导I相和II相解毒基因(分别为CYP3和GST)的转录表达,并改变了其相应酶(分别为红霉素N-脱甲基酶和谷胱甘肽S-转移酶)的表达。此外,氟苯尼考诱导了ATP结合盒(ABC)转运蛋白B亚家族(ABCB)和G亚家族(ABCG)的转录,尽管20mg/kg的氟苯尼考未诱导ABCG转录。此外,较高剂量的氟苯尼考在给药后的前48小时内造成了显著的生物分子损伤。本研究将有助于更好地理解水生生物中毒的确切机制。