| Autor: |
Peters CH; Department of Physiology and Biophysics, University of Colorado Anschutz Medical Campus, Aurora, Colorado 80045, USA; email: colin.peters@cuanschutz.edu, emily.sharpe@cuanschutz.edu, catherine.proenza@cuanschutz.edu., Sharpe EJ; Department of Physiology and Biophysics, University of Colorado Anschutz Medical Campus, Aurora, Colorado 80045, USA; email: colin.peters@cuanschutz.edu, emily.sharpe@cuanschutz.edu, catherine.proenza@cuanschutz.edu., Proenza C; Department of Physiology and Biophysics, University of Colorado Anschutz Medical Campus, Aurora, Colorado 80045, USA; email: colin.peters@cuanschutz.edu, emily.sharpe@cuanschutz.edu, catherine.proenza@cuanschutz.edu.; Department of Cardiology, University of Colorado Anschutz Medical Campus, Aurora, Colorado 80045, USA. |
| Abstrakt: |
A progressive decline in maximum heart rate (mHR) is a fundamental aspect of aging in humans and other mammals. This decrease in mHR is independent of gender, fitness, and lifestyle, affecting in equal measure women and men, athletes and couch potatoes, spinach eaters and fast food enthusiasts. Importantly, the decline in mHR is the major determinant of the age-dependent decline in aerobic capacity that ultimately limits functional independence for many older individuals. The gradual reduction in mHR with age reflects a slowing of the intrinsic pacemaker activity of the sinoatrial node of the heart, which results from electrical remodeling of individual pacemaker cells along with structural remodeling and a blunted β-adrenergic response. In this review, we summarize current evidence about the tissue, cellular, and molecular mechanisms that underlie the reduction in pacemaker activity with age and highlight key areas for future work. |
