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Angiotensin II blockade: how its molecular targets may signal to mitochondria and slow aging. Coincidences with calorie restriction and mTOR inhibition
Elena M. V. de Cavanagh, Felipe Inserra, León Ferder
American Journal of Physiology-Heart and Circulatory Physiology · 2015 · ▲ 60 citations
Epigenetic alterations
Deregulated nutrient-sensing
Mitochondrial dysfunction
Altered intercellular communication
Caloric restriction
Rapamycin / mTOR inhibition
Cell culture / in vitro
Review
Abstract
Caloric restriction(definition) (CR), renin angiotensin system blockade (RAS-bl), and mTOR(definition)-inhibiting drug studied for extending healthspan and lifespan." style="text-decoration:underline dotted; text-underline-offset:2px; cursor:help;">rapamycin(definition)-mediated mechanistic target of rapamycin (mTOR) inhibition increase survival and retard aging across species. Previously, we have summarized CR and RAS-bl's converging effects, and the mitochondrial function changes associated with their physiological benefits. mTOR inhibition and enhanced sirtuin and KLOTHO signaling contribute to the benefits of CR in aging. mTORC1/mTORC2 complexes contribute to cell growth and metabolic regulation. Prolonged mTORC1 activation may lead to age-related disease progression; thus, rapamycin-mediated mTOR inhibition and CR may extend lifespan and retard aging through mTORC1 interference. Sirtuins by deacetylating histone and transcription-related proteins modulate signaling and survival pathways and mitochondrial functioning. CR regulates several mammalian sirtuins favoring their role in aging regulation. KLOTHO/fibroblast growth factor 23 (FGF23) contribute to control Ca(2+), phosphate, and vitamin D metabolism, and their dysregulation may participate in age-related disease. Here we review how mTOR inhibition extends lifespan, how KLOTHO functions as an aging suppressor, how sirtuins mediate longevity, how vitamin D loss may contribute to age-related disease, and how they relate to mitochondrial function. Also, we discuss how RAS-bl downregulates mTOR and upregulates KLOTHO, sirtuin, and vitamin D receptor expression, suggesting that at least some of RAS-bl benefits in aging are mediated through the modulation of mTOR, KLOTHO, and sirtuin expression and vitamin D signaling, paralleling CR actions in age retardation. Concluding, the available evidence endorses the idea that RAS-bl is among the interventions that may turn out to provide relief to the spreading issue of age-associated chronic disease.
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- DOI
- 10.1152/ajpheart.00459.2014
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- 2026-06-13 MST
Cite this
APA
Cavanagh, E.M.V.D., Inserra, F., & Ferder, L. (2015). Angiotensin II blockade: how its molecular targets may signal to mitochondria and slow aging. Coincidences with calorie restriction and mTOR inhibition. <em>American Journal of Physiology-Heart and Circulatory Physiology</em>. https://doi.org/10.1152/ajpheart.00459.2014
Vancouver
Cavanagh EMVD, Inserra F, Ferder L. Angiotensin II blockade: how its molecular targets may signal to mitochondria and slow aging. Coincidences with calorie restriction and mTOR inhibition. American Journal of Physiology-Heart and Circulatory Physiology. 2015. doi:10.1152/ajpheart.00459.2014.
BibTeX
@article{elena2015Angiot,
title = {Angiotensin II blockade: how its molecular targets may signal to mitochondria and slow aging. Coincidences with calorie restriction and mTOR inhibition},
author = {Elena M. V. de Cavanagh and Felipe Inserra and León Ferder},
journal = {American Journal of Physiology-Heart and Circulatory Physiology},
year = {2015},
doi = {10.1152/ajpheart.00459.2014},
}
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