Barcena Maria Luisa, Aslam Muhammad, Norman Kristina, Ott Christiane, Ladilov Yury
Department of Urology, Eberhard Karl University of Tuebingen, Tuebingen, Germany.
Experimental Cardiology, Department of Internal Medicine I, Justus Liebig University, Giessen, Germany.
Aging Dis. 2024 Dec 3. doi: 10.14336/AD.2024.1216.
Aging is a key risk factor for numerous diseases, including cardiac diseases. High energy demands of the heart require precise cellular energy sensing to prevent metabolic stress. AMPK and sirtuins are key intracellular metabolic sensors regulating numerous cell functions, like mitochondrial function and biogenesis, autophagy, and redox balance. However, their function is impaired during the aging process leading to mitochondrial dysfunction, oxidative stress, and inflammation culminating in cardiovascular diseases. The underlying molecular mechanisms leading to dysfunction of metabolic sensing in the aging heart are complex and comprise both intracellular and systemic age-related alterations. In this study, we overview the current knowledge on the impact of aging on cardiac metabolic sensing, with a focus on AMPK and sirtuins, while mTOR pathway was only marginally considered. A particular focus was given to systemic factors, e.g., inflammation, vascular diseases, and microbiome.
衰老 是包括心脏病在内的多种疾病的关键风险因素。心脏对能量的高需求需要精确的细胞能量感知,以防止代谢应激。腺苷酸活化蛋白激酶(AMPK)和沉默调节蛋白是调节众多细胞功能(如线粒体功能与生物发生、自噬和氧化还原平衡)的关键细胞内代谢传感器。然而,它们的功能在衰老过程中受损,导致线粒体功能障碍、氧化应激和炎症,最终引发心血管疾病。导致衰老心脏中代谢感知功能障碍的潜在分子机制很复杂,包括细胞内和全身与年龄相关的改变。在本研究中,我们概述了目前关于衰老对心脏代谢感知影响的知识,重点关注AMPK和沉默调节蛋白,而对雷帕霉素靶蛋白(mTOR)途径仅作了少量考虑。我们特别关注了全身因素,如炎症、血管疾病和微生物群。