Department of Zoology/Zoophysiology, University of Gothenburg, Sweden.
Comp Biochem Physiol C Toxicol Pharmacol. 2011 Sep;154(3):234-41. doi: 10.1016/j.cbpc.2011.06.002. Epub 2011 Jun 15.
Medetomidine is under evaluation for use as an antifouling agent, and its effects on non-target aquatic organisms are therefore of interest. In this study, rainbow trout was exposed to low (0.5 and 5.0nM) concentrations of medetomidine for up to 54 days. Recently we have reported on effects on paleness and melanophore aggregation of medetomidine in these fish. Here, specific growth rates were investigated together with a broad set of physiological parameters including plasma levels of growth hormone (GH), insulin-like growth factor-I (IGF-I) and leptin, glucose and haemoglobin (Hb), hematocrit (Ht), condition factor, liver and heart somatic indexes (LSI, HSI). Hepatic enzyme activities of CYP1A (EROD activity), glutathione S-transferases (GST) and glutathione reductase (GR) were also measured. Additionally, hepatic mRNA expression was analysed through microarray and quantitative PCR in fish sampled after 31 days of exposure. Medetomidine at both concentrations significantly lowered blood glucose levels and the higher concentration significantly reduced the LSI. The mRNA expression analysis revealed few differentially expressed genes in the liver and the false discovery rate was high. Taken together, the results suggest that medetomidine at investigated concentrations could interfere with carbohydrate metabolism of exposed fish but without any clear consequences for growth.
美托咪定正被评估为一种防污剂,因此其对非目标水生生物的影响引起了人们的关注。在这项研究中,虹鳟鱼暴露于低浓度(0.5 和 5.0nM)的美托咪定中,长达 54 天。最近,我们报道了美托咪定对这些鱼类的苍白和黑色素聚集的影响。在这里,我们研究了特定生长率以及一系列广泛的生理参数,包括生长激素(GH)、胰岛素样生长因子-I(IGF-I)和瘦素、葡萄糖和血红蛋白(Hb)、血细胞比容(Ht)、条件因子、肝和心脏体指数(LSI、HSI)。还测量了 CYP1A(EROD 活性)、谷胱甘肽 S-转移酶(GST)和谷胱甘肽还原酶(GR)的肝酶活性。此外,在暴露 31 天后采集的鱼类中,通过微阵列和定量 PCR 分析了肝组织中的 mRNA 表达。两种浓度的美托咪定都显著降低了血糖水平,高浓度还显著降低了 LSI。mRNA 表达分析显示肝脏中差异表达的基因很少,错误发现率很高。综合来看,结果表明,在所研究的浓度下,美托咪定可能会干扰暴露鱼类的碳水化合物代谢,但对生长没有明显影响。