Division of Kinesiology and Health, University of Wyoming, Laramie, Wyoming, United States.
Division of Cardiology, Department of Medicine, School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States.
Am J Physiol Heart Circ Physiol. 2023 Aug 1;325(2):H278-H292. doi: 10.1152/ajpheart.00124.2023. Epub 2023 Jun 30.
Right ventricular (RV) function is the strongest predictor of survival in age-related heart failure as well as other clinical contexts in which aging populations suffer significant morbidity and mortality. However, despite the significance of maintaining RV function with age and disease, mechanisms of RV failure remain poorly understood and no RV-directed therapies exist. The antidiabetic drug and AMP-activated protein kinase (AMPK) activator metformin protects against left ventricular dysfunction, suggesting cardioprotective properties may translate to the RV. Here, we aimed to understand the impact of advanced age on pulmonary hypertension (PH)-induced right ventricular dysfunction. We further aimed to test whether metformin is cardioprotective in the RV and whether the protection afforded by metformin requires cardiac AMPK. We used a murine model of PH by exposing adult (4-6 mo) and aged (18 mo) male and female mice to hypobaric hypoxia (HH) for 4 wk. Cardiopulmonary remodeling was exacerbated in aged mice compared with adult mice as evidenced by elevated RV weight and impaired RV systolic function. Metformin attenuated HH-induced RV dysfunction but only in adult male mice. Metformin still protected the adult male RV even in the absence of cardiac AMPK. Together, we suggest that aging exacerbates PH-induced RV remodeling and that metformin may represent a therapeutic option for this disease in a sex- and age-dependent manner, but in an AMPK-independent manner. Ongoing efforts are aimed at elucidating the molecular basis for RV remodeling as well as delineating the mechanisms of cardioprotection provided by metformin in the absence of cardiac AMPK. Right ventricular (RV) function predicts survival in age-related disease, yet mechanisms of RV failure are unclear. We show that aged mice undergo exacerbated RV remodeling compared with young. We tested the AMPK activator metformin to improve RV function and show that metformin attenuates RV remodeling only in adult male mice via a mechanism that does not require cardiac AMPK. Metformin is therapeutic for RV dysfunction in an age- and sex-specific manner independent of cardiac AMPK.
右心室(RV)功能是与年龄相关的心力衰竭以及其他老龄化人群发病率和死亡率较高的临床情况下的最强生存预测因子。然而,尽管随着年龄和疾病的增长而保持 RV 功能的意义重大,但 RV 衰竭的机制仍知之甚少,也不存在 RV 靶向治疗方法。抗糖尿病药物和 AMP 激活的蛋白激酶(AMPK)激活剂二甲双胍可预防左心室功能障碍,这表明其具有心脏保护作用,可能适用于 RV。在这里,我们旨在了解高龄对肺动脉高压(PH)引起的 RV 功能障碍的影响。我们进一步旨在测试二甲双胍是否对 RV 具有心脏保护作用,以及二甲双胍提供的保护是否需要心脏 AMPK。我们使用成年(4-6 个月)和老年(18 个月)雄性和雌性小鼠暴露于低气压缺氧(HH)4 周的 PH 小鼠模型。与成年小鼠相比,老年小鼠的心肺重塑更为严重,表现为 RV 重量增加和 RV 收缩功能受损。二甲双胍可减轻 HH 引起的 RV 功能障碍,但仅在成年雄性小鼠中。即使在没有心脏 AMPK 的情况下,二甲双胍仍能保护成年雄性 RV。总之,我们认为衰老会加重 PH 引起的 RV 重塑,并且二甲双胍可能以性别和年龄依赖的方式成为该疾病的治疗选择,但不依赖心脏 AMPK。目前正在努力阐明 RV 重塑的分子基础,并阐明在没有心脏 AMPK 的情况下二甲双胍提供的心脏保护机制。