| Autor: |
Mahoney SA; Department of Integrative Physiology, University of Colorado Boulder, Boulder, Colorado, United States., VanDongen NS; Department of Integrative Physiology, University of Colorado Boulder, Boulder, Colorado, United States., Greenberg NT; Department of Integrative Physiology, University of Colorado Boulder, Boulder, Colorado, United States., Venkatasubramanian R; Department of Integrative Physiology, University of Colorado Boulder, Boulder, Colorado, United States., Rossman MJ; Department of Integrative Physiology, University of Colorado Boulder, Boulder, Colorado, United States., Widlansky ME; Department of Medicine and Pharmacology, Medical College of Wisconsin, Milwaukee, Wisconsin, United States., Brunt VE; Department of Integrative Physiology, University of Colorado Boulder, Boulder, Colorado, United States.; Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States., Bernaldo de Quirós Y; Department of Integrative Physiology, University of Colorado Boulder, Boulder, Colorado, United States.; Institute of Animal Health and Food Safety, Universidad de Las Palmas de Gran Canaria, Canary Islands, Spain., Seals DR; Department of Integrative Physiology, University of Colorado Boulder, Boulder, Colorado, United States., Clayton ZS; Department of Integrative Physiology, University of Colorado Boulder, Boulder, Colorado, United States. |
| Abstrakt: |
The circulating milieu, bioactive molecules in the bloodstream, is altered with aging and interfaces constantly with the vasculature. This anatomic juxtaposition suggests that circulating factors may actively modulate arterial function. Here, we developed a novel, translational experimental model that allows for direct interrogation of the influence of the circulating milieu on age-related arterial dysfunction (aortic stiffening and endothelial dysfunction). To do so, we exposed young and old mouse arteries to serum from young and old mice and young and midlife/older (ML/O) adult humans. We found that old mouse and ML/O adult human, but not young, serum stiffened young mouse aortic rings, assessed via elastic modulus (mouse and human serum, P = 0.003 vs. young serum control), and impaired carotid artery endothelial function, assessed by endothelium-dependent dilation (EDD) (mouse serum, P < 0.001; human serum, P = 0.006 vs. young serum control). Furthermore, young mouse and human, but not old, serum reduced aortic elastic modulus (mouse serum, P = 0.009; human serum, P < 0.001 vs. old/MLO serum control) and improved EDD (mouse and human serum, P = 0.015 vs. old/MLO serum control) in old arteries. In human serum-exposed arteries, in vivo arterial function assessed in the human donors correlated with circulating milieu-modulated arterial function in young mouse arteries (aortic stiffness, r = 0.634, P = 0.005; endothelial function, r = 0.609, P = 0.004) and old mouse arteries (aortic stiffness, r = 0.664, P = 0.001; endothelial function, r = 0.637, P = 0.003). This study establishes novel experimental approaches for directly assessing the effects of the circulating milieu on arterial function and implicates changes in the circulating milieu as a mechanism of in vivo arterial aging. NEW & NOTEWORTHY Changes in the circulating milieu with advancing age may be a mechanism underlying age-related arterial dysfunction. Ex vivo exposure of young mouse arteries to the circulating milieu from old mice or midlife/older adults impairs arterial function whereas exposure of old mouse arteries to the circulating milieu from young mice or young adults improves arterial function. These findings establish that the circulating milieu directly influences arterial function with aging. |
