Johansen Ida B, Sandblom Erik, Skov Peter V, Gräns Albin, Ekström Andreas, Lunde Ida G, Vindas Marco A, Zhang Lili, Höglund Erik, Frisk Michael, Sjaastad Ivar, Nilsson Göran E, Øverli Øyvind
Department of Biosciences, University of Oslo, Blindern, 0316 Oslo, Norway
Bjørknes College, 0456 Oslo, Norway.
J Exp Biol. 2017 Jul 15;220(Pt 14):2545-2553. doi: 10.1242/jeb.135046. Epub 2017 May 5.
Stress and elevated cortisol levels are associated with pathological heart growth and cardiovascular disease in humans and other mammals. We recently established a link between heritable variation in post-stress cortisol production and cardiac growth in salmonid fish too. A conserved stimulatory effect of the otherwise catabolic steroid hormone cortisol is probably implied, but has to date not been established experimentally. Furthermore, whereas cardiac growth is associated with failure of the mammalian heart, pathological cardiac hypertrophy has not previously been described in fish. Here, we show that rainbow trout () treated with cortisol in the diet for 45 days have enlarged hearts with lower maximum stroke volume and cardiac output. In accordance with impaired cardiac performance, overall circulatory oxygen-transporting capacity was diminished as indicated by reduced aerobic swimming performance. In contrast to the well-known adaptive/physiological heart growth observed in fish, cortisol-induced growth is maladaptive. Furthermore, the observed heart growth was associated with up-regulated signature genes of mammalian cardiac pathology, suggesting that signalling pathways mediating cortisol-induced cardiac remodelling in fish are conserved from fish to mammals. Altogether, we show that excessive cortisol can induce pathological cardiac remodelling. This is the first study to report and integrate the etiology, physiology and molecular biology of cortisol-induced pathological remodelling in fish.
压力和皮质醇水平升高与人类和其他哺乳动物的病理性心脏生长及心血管疾病有关。我们最近也在鲑科鱼类中建立了应激后皮质醇产生的遗传变异与心脏生长之间的联系。可能意味着分解代谢类固醇激素皮质醇具有保守的刺激作用,但迄今为止尚未通过实验证实。此外,虽然心脏生长与哺乳动物心脏功能衰竭有关,但鱼类中此前尚未描述过病理性心脏肥大。在此,我们表明,在饮食中用皮质醇处理45天的虹鳟鱼心脏增大,最大搏出量和心输出量降低。与心脏功能受损一致,有氧游泳能力下降表明整体循环氧运输能力降低。与鱼类中观察到的众所周知的适应性/生理性心脏生长不同,皮质醇诱导的生长是适应不良的。此外,观察到的心脏生长与哺乳动物心脏病理学的标志性基因上调有关,这表明介导鱼类皮质醇诱导的心脏重塑的信号通路从鱼类到哺乳动物是保守的。总之,我们表明过量的皮质醇可诱导病理性心脏重塑。这是第一项报告并整合鱼类中皮质醇诱导的病理性重塑的病因、生理学和分子生物学的研究。