Vijayan M M, Reddy P K, Leatherland J F, Moon T W
Ottawa-Carleton Institute of Biology, Department of Biology, University of Ottawa, Ontario, Canada.
Gen Comp Endocrinol. 1994 Oct;96(1):75-84. doi: 10.1006/gcen.1994.1160.
The objective of this study was to examine if RU486, a corticosteroid antagonist, modified hepatocyte metabolism and blocked the metabolic effects of exogenously administered cortisol in rainbow trout (Oncorhynchus mykiss). The fish were given a single intraperitoneal implant of either coconut oil alone or coconut oil containing RU486 (100 mg.kg-1), cortisol (100 mg.kg-1), or a combination of RU486 and cortisol and were sampled 7 days postimplantation. The RU486 implants had no effect on plasma cortisol and glucose concentrations, hepatocyte glycogen content, and total glucose production, but increased in vitro hepatocyte glycogen breakdown. Cortisol implantation had no effect on plasma glucose concentration, hepatocyte glycogen content, glycogen breakdown, or total glucose production, while it significantly increased alanine oxidation and gluconeogenesis in rainbow trout hepatocytes. Hepatocyte responsiveness to epinephrine and glucagon stimulation of total glucose production was not modified by either RU486 or cortisol treatment, whereas the insulin response on total glucose production was decreased with cortisol. RU486 treatment modified hepatocyte glycogen metabolism and blocked the cortisol-induced increases in alanine gluconeogenesis and glycogen mobilization for endogenous use by the hepatocytes. These results indicate that cortisol enhances the metabolic potential of hepatocytes, thereby adapting the fish to cope with stress. This study provides further validation of RU486 as a tool for studying metabolic actions of cortisol in fish.
本研究的目的是检验皮质类固醇拮抗剂RU486是否会改变虹鳟鱼(Oncorhynchus mykiss)肝细胞的代谢,并阻断外源性给予皮质醇的代谢作用。给鱼腹腔内单次植入单独的椰子油或含RU486(100毫克·千克⁻¹)、皮质醇(100毫克·千克⁻¹)或RU486与皮质醇组合的椰子油,并在植入后7天取样。植入RU486对血浆皮质醇和葡萄糖浓度、肝细胞糖原含量以及总葡萄糖生成没有影响,但增加了体外肝细胞糖原分解。植入皮质醇对血浆葡萄糖浓度、肝细胞糖原含量、糖原分解或总葡萄糖生成没有影响,而它显著增加了虹鳟鱼肝细胞中的丙氨酸氧化和糖异生。RU486或皮质醇处理均未改变肝细胞对肾上腺素和胰高血糖素刺激总葡萄糖生成的反应性,而皮质醇降低了胰岛素对总葡萄糖生成的反应。RU486处理改变了肝细胞糖原代谢,并阻断了皮质醇诱导的丙氨酸糖异生增加以及肝细胞内源性糖原动员增加。这些结果表明,皮质醇增强了肝细胞的代谢潜力,从而使鱼能够适应应激。本研究进一步验证了RU486作为研究鱼类皮质醇代谢作用工具的有效性。