Gent Sabine, Kleinbongard Petra, Dammann Philip, Neuhäuser Markus, Heusch Gerd
Institute for Pathophysiology, West German Heart and Vascular Center, University School of Medicine, Hufelandstr. 55, 45122, Essen, Germany.
Basic Res Cardiol. 2015 Mar;110(2):2. doi: 10.1007/s00395-014-0460-7. Epub 2015 Jan 15.
Heart rate correlates inversely with life span across all species, including humans. In patients with cardiovascular disease, higher heart rate is associated with increased mortality, and such patients benefit from pharmacological heart rate reduction. However, cause-and-effect relationships between heart rate and longevity, notably in healthy individuals, are not established. We therefore prospectively studied the effects of a life-long pharmacological heart rate reduction on longevity in mice. We hypothesized, that the total number of cardiac cycles is constant, and that a 15% heart rate reduction might translate into a 15% increase in life span. C57BL6/J mice received either placebo or ivabradine at a dose of 50 mg/kg/day in drinking water from 12 weeks to death. Heart rate and body weight were monitored. Autopsy was performed on all non-autolytic cadavers, and parenchymal organs were evaluated macroscopically. Ivabradine reduced heart rate by 14% (median, interquartile range 12-15%) throughout life, and median life span was increased by 6.2% (p = 0.01). Body weight and macroscopic findings were not different between placebo and ivabradine. Life span was not increased to the same extent as heart rate was reduced, but nevertheless significantly prolonged by 6.2%.
在包括人类在内的所有物种中,心率与寿命呈负相关。在心血管疾病患者中,较高的心率与死亡率增加相关,此类患者可从药物降低心率中获益。然而,心率与寿命之间的因果关系,尤其是在健康个体中,尚未确立。因此,我们前瞻性地研究了终身药物降低心率对小鼠寿命的影响。我们假设,心动周期总数是恒定的,心率降低15%可能转化为寿命延长15%。C57BL6/J小鼠从12周龄至死亡期间,在饮水中接受安慰剂或50 mg/kg/天剂量的伊伐布雷定。监测心率和体重。对所有未自溶的尸体进行尸检,并对实质器官进行宏观评估。伊伐布雷定在整个生命过程中将心率降低了14%(中位数,四分位间距12 - 15%),中位寿命增加了6.2%(p = 0.01)。安慰剂组和伊伐布雷定组之间的体重和宏观检查结果无差异。寿命延长的幅度与心率降低的幅度不同,但仍显著延长了6.2%。