Interdisciplinary Centre of Marine and Environmental Research (CIIMAR/CIMAR), University of Porto (U.Porto), Terminal de Cruzeiros do Porto de Leixões, Av. General Norton de Matos s/n, 4450-208 Matosinhos, Portugal; Institute of Biomedical Sciences Abel Salazar (ICBAS), University of Porto (U. Porto), Laboratory of Histology and Embryology, Department of Microscopy, Rua Jorge Viterbo Ferreira 228, P 4050-313 Porto, Portugal.
Interdisciplinary Centre of Marine and Environmental Research (CIIMAR/CIMAR), University of Porto (U.Porto), Terminal de Cruzeiros do Porto de Leixões, Av. General Norton de Matos s/n, 4450-208 Matosinhos, Portugal; Institute of Biomedical Sciences Abel Salazar (ICBAS), University of Porto (U. Porto), Laboratory of Histology and Embryology, Department of Microscopy, Rua Jorge Viterbo Ferreira 228, P 4050-313 Porto, Portugal.
Comp Biochem Physiol C Toxicol Pharmacol. 2018 Oct;212:1-17. doi: 10.1016/j.cbpc.2018.06.001. Epub 2018 Jun 7.
Lipid metabolism involves complex pathways, which are regulated in a similar way across vertebrates. Hormonal and hypolipidemic deregulations cause lipid imbalance from fish to humans, but the underlying mechanisms are far from understood. This study explores the potential of using juvenile brown trout to evaluate the in vivo interferences caused by estrogenic (17α-ethinylestradiol - EE2), androgenic (testosterone - T), and hypolipidemic (clofibrate - CLF) compounds in lipidic and/or peroxisomal pathways. Studied endpoints were from blood/plasma biochemistry, plasma fatty acid profile, ultrastructure of hepatocytes and abundance of their peroxisomes to mRNA expression in the liver. Both T and CLF caused minimal effects when compared to EE2. Estrogenized fish had significantly higher hepatosomatic indexes, increased triglycerides and very-low density lipoproteins (VLDL) in plasma, compared with solvent control. Morphologically, EE2 fish showed increased lipid droplets in hepatocytes, and EE2 and T reduced volume density of peroxisomes in relation to the hepatic parenchyma. Polyunsaturated fatty acids (PUFA) in plasma, namely n-3 PUFA, increased with EE2. EE2 animals had increased mRNA levels of vitellogenin A (VtgA), estrogen receptor alpha (ERα), peroxisome proliferator-activated receptor alpha (PPARα), PPARαBa and acyl-CoA long chain synthetase 1 (Acsl1), while ERβ-1, acyl-CoA oxidase 1-3I (Acox1-3I), Acox3, PPARγ, catalase (Cat), urate oxidase (Uox), fatty acid binding protein 1 (Fabp1) and apolipoprotein AI (ApoAI) were down-regulated. In summary, in vivo EE2 exposure altered lipid metabolism and peroxisome dynamics in brown trout, namely by changing the mRNA levels of several genes. Our model can be used to study possible organism-level impacts, viz. in gonadogenesis.
脂质代谢涉及复杂的途径,这些途径在脊椎动物中以相似的方式受到调节。从鱼类到人类,激素和降血脂紊乱会导致脂质失衡,但潜在机制还远未被理解。本研究探索了利用幼年褐鳟鱼来评估雌激素(17α-乙炔基雌二醇 - EE2)、雄激素(睾酮 - T)和降血脂(氯贝特 - CLF)化合物在脂质和/或过氧化物酶体途径中引起的体内干扰的潜力。研究的终点是从血液/血浆生化、血浆脂肪酸谱、肝细胞超微结构及其过氧化物酶体的丰度到肝脏中的 mRNA 表达。与 EE2 相比,T 和 CLF 的影响最小。与溶剂对照相比,雌激素化鱼类的肝体比指数显著升高,血浆中的甘油三酯和极低密度脂蛋白(VLDL)增加。形态学上,EE2 鱼类的肝细胞中出现了更多的脂质滴,EE2 和 T 降低了过氧化物体相对于肝实质的体积密度。血浆中多不饱和脂肪酸(PUFA),即 n-3 PUFA,随着 EE2 的增加而增加。EE2 动物的卵黄蛋白原 A(VtgA)、雌激素受体 α(ERα)、过氧化物酶体增殖物激活受体 α(PPARα)、PPARαBa 和长链酰基辅酶 A 合成酶 1(Acsl1)的 mRNA 水平升高,而 ERβ-1、酰基辅酶 A 氧化酶 1-3I(Acox1-3I)、Acox3、PPARγ、过氧化氢酶(Cat)、尿酸氧化酶(Uox)、脂肪酸结合蛋白 1(Fabp1)和载脂蛋白 AI(ApoAI)的 mRNA 水平下调。总之,体内 EE2 暴露改变了褐鳟鱼的脂质代谢和过氧化物体动态,即通过改变几个基因的 mRNA 水平。我们的模型可用于研究可能的机体水平影响,例如在性腺发生中。