Department of Basic Sciences and Aquatic Medicine, Norwegian School of Veterinary Science, P.O. Box 8146 Dep, Ullevålsveien 72, N-0033, Oslo, Norway.
Physiol Behav. 2009 Dec 7;98(5):625-30. doi: 10.1016/j.physbeh.2009.09.018. Epub 2009 Oct 6.
The present study has investigated the effect of exogenous cortisol on aggression in juvenile rainbow trout, along with the involvement of mineralocorticoid (MR) and glucocorticoid receptors (GR) mediating the effects of cortisol. Fish were fed pellets supplemented with cortisol, the GR antagonist mifepristone (RU486) in combination with cortisol, the MR antagonist spironolactone (SA) in combination with cortisol or both antagonists in combination with cortisol. Aggressive behaviour was then assessed 1h subsequent to feeding. Our results showed that the attack latency was increased by exogenous cortisol, an effect that was not abolished by the antagonists. The intensity of aggression was not changed by exogenous cortisol. However, the intensity of aggression was significantly reduced by both antagonists. These results are discussed with regard to cortisol affecting aggressive behaviour through genomic and non-genomic pathways. Our results have demonstrated the involvement of both MR and GR in regulating behavioural responses during social interactions in teleost fish. The intensity of aggression seen in control and cortisol treated fish is probably mediated by the basal levels of cortisol through the intracellular MRs and GRs. We conclude that the initiative to engage in social confrontations is mediated through a non-genomic pathway, which could involve extracellular corticoid receptors. Further, the majority of arguments lean towards the MR and GR antagonists blocking the effect of cortisol on aggressive intensity through intracellular receptors. If this is the case, then it is probable that these two aspects of aggressive behaviour are based on different neuronal mechanisms.
本研究调查了外源性皮质醇对幼彩虹鳟鱼攻击性的影响,以及参与皮质醇作用的盐皮质激素(MR)和糖皮质激素受体(GR)。鱼被喂食补充了皮质醇的颗粒,皮质醇与 GR 拮抗剂米非司酮(RU486)联合,皮质醇与 MR 拮抗剂螺内酯(SA)联合,或两种拮抗剂与皮质醇联合。然后在喂食后 1 小时评估攻击行为。我们的结果表明,外源性皮质醇增加了攻击潜伏期,而拮抗剂并没有消除这种作用。攻击性的强度没有被外源性皮质醇改变。然而,两种拮抗剂都显著降低了攻击性的强度。这些结果与皮质醇通过基因组和非基因组途径影响攻击性行为有关。我们的结果表明,MR 和 GR 都参与了调节硬骨鱼在社会互动中的行为反应。对照组和皮质醇处理组鱼的攻击性强度可能是通过细胞内的 MR 和 GR 由基础水平的皮质醇介导的。我们得出结论,参与社会对抗的主动权是通过非基因组途径介导的,这可能涉及细胞外皮质激素受体。此外,大多数观点倾向于 MR 和 GR 拮抗剂通过细胞内受体阻断皮质醇对攻击性强度的影响。如果是这样,那么这两种攻击性行为可能基于不同的神经元机制。