Physiologisches Institut, Justus-Liebig-Universität, 35392 Gießen, Germany.
Universitätsklinikum Gießen, Klinik für Herz-, Kinderherz- und Gefäßchirurgie, 35392 Gießen, Germany.
Cells. 2020 Feb 27;9(3):552. doi: 10.3390/cells9030552.
The cardiac expression of the mitochondrial uncoupling protein (UCP)-2 is increased in patients with heart failure. However, the underlying causes as well as the possible consequences of these alterations during the transition from hypertrophy to heart failure are still unclear. To investigate the role of UCP-2 mechanistically, expression of UCP-2 was silenced by small interfering RNA in adult rat ventricular cardiomyocytes. We demonstrate that a downregulation of UCP-2 by siRNA in cardiomyocytes preserves contractile function in the presence of angiotensin II. Furthermore, silencing of UCP-2 was associated with an upregulation of glucose transporter type (Glut)-4, increased glucose uptake, and reduced intracellular lactate levels, indicating improvement of the oxidative glucose metabolism. To study this adaptation in vivo, spontaneously hypertensive rats served as a model for cardiac hypertrophy due to pressure overload. During compensatory hypertrophy, we found low UCP-2 levels with an upregulation of Glut-4, while the decompensatory state with impaired function was associated with an increase of UCP-2 and reduced Glut-4 expression. By blocking the aldosterone receptor with spironolactone, both cardiac function as well as UCP-2 and Glut-4 expression levels of the compensated phase could be preserved. Furthermore, we were able to confirm this by left ventricular (LV) biopsies of patients with end-stage heart failure. The results of this study show that UCP-2 seems to impact the cardiac glucose metabolism during the transition from hypertrophy to failure by affecting glucose uptake through Glut-4. We suggest that the failing heart could benefit from low UCP-2 levels by improving the efficiency of glucose oxidation. For this reason, UCP-2 inhibition might be a promising therapeutic strategy to prevent the development of heart failure.
心脏线粒体解偶联蛋白(UCP)-2 的表达在心力衰竭患者中增加。然而,在从心肌肥厚向心力衰竭转变过程中,这些改变的潜在原因以及可能的后果仍不清楚。为了从机制上研究 UCP-2 的作用,我们通过小干扰 RNA 沉默成年大鼠心室肌细胞中的 UCP-2 表达。我们证明,在血管紧张素 II 存在的情况下,心肌细胞中 UCP-2 的下调通过 siRNA 可维持收缩功能。此外,UCP-2 的沉默与葡萄糖转运体类型(Glut)-4 的上调、葡萄糖摄取增加和细胞内乳酸水平降低有关,表明氧化葡萄糖代谢得到改善。为了在体内研究这种适应,自发性高血压大鼠作为心脏肥厚的模型,由于压力超负荷。在代偿性肥厚期间,我们发现 UCP-2 水平低,Glut-4 上调,而功能受损的失代偿状态与 UCP-2 增加和 Glut-4 表达减少有关。通过用螺内酯阻断醛固酮受体,可以维持代偿期的心脏功能以及 UCP-2 和 Glut-4 的表达水平。此外,我们还可以通过心力衰竭终末期患者的左心室(LV)活检来证实这一点。这项研究的结果表明,UCP-2 通过影响 Glut-4 摄取来影响从肥厚到衰竭的心脏葡萄糖代谢,因此在从肥厚向衰竭的转变过程中似乎会影响心脏葡萄糖代谢。我们认为,通过改善葡萄糖氧化效率,衰竭的心脏可能会受益于低水平的 UCP-2。因此,UCP-2 抑制可能是预防心力衰竭发展的一种有前途的治疗策略。