Han Xiaowei, Ashraf Muhammad, Shi Hong, Nkembo Augustine T, Tipparaju Srinivas M, Xuan Wanling
Department of Pharmaceutical Sciences, USF Health Taneja College of Pharmacy, University of South Florida, Tampa, FL, USA.
Division of Rheumatology, Department of Internal Medicine, Vascular Biology Center, Augusta University, Augusta, GA, USA.
Adv Biol (Weinh). 2024 May 21:e2400137. doi: 10.1002/adbi.202400137.
Aging is associated with a decline in cardiac function. Exercise has been shown to effectively reduce the risks of cardiovascular diseases. Here whether a combination of endurance and resistance exercises can improve cardiac function in aged mice during late life is investigated. Through transcriptome analysis, several signaling pathways activated in the hearts of 22-month-old mice after combined exercise, including cardiac muscle contraction, mitophagy, and longevity regulation are identified. Combined exercise training mitigated age-associated pathological cardiac hypertrophy, reduced oxidative stress, cardiac senescence, and enhanced cardiac function. Upstream stimulatory factor 2 (Usf2) is upregulated in the aged mouse hearts with combined exercise compared to sedentary mice. In the human cardiomyocytes senescent model, overexpression of Usf2 led to anti-senescence effects, while knockdown of Usf2 exacerbated cellular senescence. The results suggest that a combination of endurance and resistance exercises, such as swimming and resistance running, can mitigate age-related pathological cardiac remodeling and cardiac dysfunction in late life. These cardioprotective effects are likely due to the activation of Usf2 and its anti-senescence effect. Therefore, Usf2 can potentially be a novel therapeutic target for mitigating age-related cardiac dysfunction.
衰老与心脏功能衰退有关。运动已被证明能有效降低心血管疾病的风险。在此,研究了耐力运动和抗阻运动相结合是否能在老年小鼠晚年改善其心脏功能。通过转录组分析,确定了22月龄小鼠在联合运动后心脏中激活的几种信号通路,包括心肌收缩、线粒体自噬和寿命调节。联合运动训练减轻了与年龄相关的病理性心脏肥大,降低了氧化应激和心脏衰老,并增强了心脏功能。与久坐不动的小鼠相比,联合运动使老年小鼠心脏中的上游刺激因子2(Usf2)上调。在人类心肌细胞衰老模型中,Usf2的过表达导致抗衰老作用,而Usf2的敲低则加剧了细胞衰老。结果表明,耐力运动和抗阻运动相结合,如游泳和抗阻跑步,可以减轻晚年与年龄相关的病理性心脏重塑和心脏功能障碍。这些心脏保护作用可能归因于Usf2的激活及其抗衰老作用。因此,Usf2有可能成为减轻与年龄相关的心脏功能障碍的新型治疗靶点。