Cellular Senescence Contributes to Large Elastic Artery Stiffening and Endothelial Dysfunction With Aging: Amelioration With Senolytic Treatment

Here, we assessed the role of cellular senescence and the senescence associated secretory phenotype (SASP) in age-related aortic stiffening and endothelial dysfunction. We studied young (6-8 mo) and old (27-29 mo) p16-3MR mice, which allows for genetic-based clearance of senescent cells with gancicl...

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Veröffentlicht in:Hypertension (Dallas, Tex. 1979) Tex. 1979), 2023-10, Vol.80 (10), p.2072-2087
Hauptverfasser: Clayton, Zachary S, Rossman, Matthew J, Mahoney, Sophia A, Venkatasubramanian, Ravinandan, Maurer, Grace S, Hutton, David A, VanDongen, Nicholas S, Greenberg, Nathan T, Longtine, Abigail G, Ludwig, Katelyn R, Brunt, Vienna E, LaRocca, Thomas J, Campisi, Judith, Melov, Simon, Seals, Douglas R
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Sprache:eng
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Zusammenfassung:Here, we assessed the role of cellular senescence and the senescence associated secretory phenotype (SASP) in age-related aortic stiffening and endothelial dysfunction. We studied young (6-8 mo) and old (27-29 mo) p16-3MR mice, which allows for genetic-based clearance of senescent cells with ganciclovir (GCV). We also treated old C57BL/6N mice with the senolytic ABT-263. In old mice, GCV reduced aortic stiffness assessed by aortic pulse wave velocity (PWV; 477±10 vs. 382±7 cm/s,
ISSN:0194-911X
1524-4563
1524-4563
DOI:10.1161/HYPERTENSIONAHA.123.21392