Reproductive Medicine and Genetics, Chengdu Jinjiang Hospital for Maternal and Child Health Care, Chengdu 610066, China.
Translational Medical Center, Second Affiliated Hospital of Shantou University Medical College, Shantou, Guangdong 515041, China.
Aging (Albany NY). 2022 Mar 28;14(6):2695-2719. doi: 10.18632/aging.203967.
The beneficial effects of caloric restriction (CR) against cardiac aging and for prevention of cardiovascular diseases are numerous. However, to our knowledge, there is no scientific evidence about how a high-calorie diet (HCD) background influences the mechanisms underlying CR in whole heart tissue (WHT) in experimental murine models. In the current study, CR-treated mice with different alimentary backgrounds were subjected to transthoracic echocardiographic measurements. WHT was then analyzed to determine cardiac energetics, telomerase activity, the expression of energy-sensing networks, tissue-specific adiponectin, and cardiac precursor/cardiac stem cell markers. Animals with a balanced diet consumption before CR presented marked cardiac remodeling with improved ejection fraction (EF) and fractional shortening (FS), enhanced OXPHOS complex I, III, and IV, and CKMT2 enzymatic activity. Mice fed an HCD before CR presented moderate changes in cardiac geometry with diminished EF and FS values, but improved OXPHOS complex IV and CKMT2 activity. Differences in cardiac remodeling, left ventricular systolic/diastolic performance, and mitochondrial energetics, found in the CR-treated mice with contrasting alimentary backgrounds, were corroborated by inconsistencies in the expression of mitochondrial-biogenesis-related markers and associated regulatory networks. In particular, disruption of eNOS and AMPK -PGC-1α-mTOR-related axes. The impact of a past habit of caloric overload on the effects of CR in the WHT is a scarcely explored subject that requires deeper study in combination with analyses of other tissues and organs at higher levels of organization within the organ system. Such research will eventually lead to the development of preventative and therapeutic strategies to promote health and longevity.
热量限制(CR)对心脏衰老和心血管疾病预防的有益作用不胜枚举。然而,据我们所知,尚无科学证据表明高卡路里饮食(HCD)背景如何影响实验鼠模型整体心脏组织(WHT)中 CR 的机制。在目前的研究中,具有不同饮食背景的 CR 处理小鼠接受了经胸超声心动图测量。然后分析 WHT 以确定心脏能量学、端粒酶活性、能量感应网络的表达、组织特异性脂联素和心脏前体细胞/心脏干细胞标志物。在 CR 之前消耗均衡饮食的动物表现出明显的心脏重构,射血分数(EF)和缩短分数(FS)提高,OXPHOS 复合物 I、III 和 IV 增强,CKMT2 酶活性增强。在 CR 之前摄入 HCD 的小鼠心脏几何形状发生适度变化,EF 和 FS 值降低,但 OXPHOS 复合物 IV 和 CKMT2 活性提高。具有不同饮食背景的 CR 处理小鼠的心脏重构、左心室收缩/舒张功能和线粒体能量学的差异,与线粒体生物发生相关标志物和相关调节网络的表达不一致相吻合。特别是 eNOS 和 AMPK-PGC-1α-mTOR 相关轴的中断。过去热量超负荷习惯对 WHT 中 CR 效果的影响是一个尚未深入探讨的课题,需要与器官系统内更高组织水平的其他组织和器官的分析相结合进行更深入的研究。此类研究最终将导致预防和治疗策略的发展,以促进健康和长寿。