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Mitochondrial health is enhanced in rats with higher vs. lower intrinsic exercise capacity and extended lifespan.
Aon, Miguel A; Cortassa, Sonia; Juhaszova, Magdalena; González-Reyes, José A; Calvo-Rubio, Miguel; Villalba, José M; Lachance, Andrew D; Ziman, Bruce D; Mitchell, Sarah J; Murt, Kelsey N; Axsom, Jessie E C; Alfaras, Irene; Britton, Steven L; Koch, Lauren G; de Cabo, Rafael; Lakatta, Edward G; Sollott, Steven J.
Afiliación
  • Aon MA; Laboratory of Cardiovascular Science, National Institute on Aging, NIH, Baltimore, MD, 21224, USA. miguel.aon@nih.gov.
  • Cortassa S; Experimental Gerontology Section, Translational Gerontology Branch, National Institute on Aging, NIH, Baltimore, MD, 21224, USA. miguel.aon@nih.gov.
  • Juhaszova M; Laboratory of Cardiovascular Science, National Institute on Aging, NIH, Baltimore, MD, 21224, USA.
  • González-Reyes JA; Laboratory of Cardiovascular Science, National Institute on Aging, NIH, Baltimore, MD, 21224, USA.
  • Calvo-Rubio M; Departamento de Biología Celular, Fisiología e Inmunología, Campus de Excelencia Internacional Agroalimentario, ceiA3, Universidad de Córdoba, Córdoba, Spain.
  • Villalba JM; Departamento de Biología Celular, Fisiología e Inmunología, Campus de Excelencia Internacional Agroalimentario, ceiA3, Universidad de Córdoba, Córdoba, Spain.
  • Lachance AD; Departamento de Biología Celular, Fisiología e Inmunología, Campus de Excelencia Internacional Agroalimentario, ceiA3, Universidad de Córdoba, Córdoba, Spain.
  • Ziman BD; Laboratory of Cardiovascular Science, National Institute on Aging, NIH, Baltimore, MD, 21224, USA.
  • Mitchell SJ; Laboratory of Cardiovascular Science, National Institute on Aging, NIH, Baltimore, MD, 21224, USA.
  • Murt KN; Experimental Gerontology Section, Translational Gerontology Branch, National Institute on Aging, NIH, Baltimore, MD, 21224, USA.
  • Axsom JEC; Harvard T.H. Chan School of Public Health, Boston, MA, 02115, USA.
  • Alfaras I; Experimental Gerontology Section, Translational Gerontology Branch, National Institute on Aging, NIH, Baltimore, MD, 21224, USA.
  • Britton SL; Laboratory of Cardiovascular Science, National Institute on Aging, NIH, Baltimore, MD, 21224, USA.
  • Koch LG; Experimental Gerontology Section, Translational Gerontology Branch, National Institute on Aging, NIH, Baltimore, MD, 21224, USA.
  • de Cabo R; Department of Medicine, Aging Institute, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
  • Lakatta EG; Department of Anesthesiology, University of Michigan, Ann Arbor, MI, USA.
  • Sollott SJ; Molecular and Integrative Physiology, University of Michigan, Ann Arbor, MI, USA.
NPJ Aging Mech Dis ; 7(1): 1, 2021 Jan 04.
Article en En | MEDLINE | ID: mdl-33398019
The intrinsic aerobic capacity of an organism is thought to play a role in aging and longevity. Maximal respiratory rate capacity, a metabolic performance measure, is one of the best predictors of cardiovascular- and all-cause mortality. Rats selectively bred for high-(HCR) vs. low-(LCR) intrinsic running-endurance capacity have up to 31% longer lifespan. We found that positive changes in indices of mitochondrial health in cardiomyocytes (respiratory reserve, maximal respiratory capacity, resistance to mitochondrial permeability transition, autophagy/mitophagy, and higher lipids-over-glucose utilization) are uniformly associated with the extended longevity in HCR vs. LCR female rats. Cross-sectional heart metabolomics revealed pathways from lipid metabolism in the heart, which were significantly enriched by a select group of strain-dependent metabolites, consistent with enhanced lipids utilization by HCR cardiomyocytes. Heart-liver-serum metabolomics further revealed shunting of lipidic substrates between the liver and heart via serum during aging. Thus, mitochondrial health in cardiomyocytes is associated with extended longevity in rats with higher intrinsic exercise capacity and, probably, these findings can be translated to other populations as predictors of outcomes of health and survival.

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: NPJ Aging Mech Dis Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: NPJ Aging Mech Dis Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos