Age is the major risk factor for many diseases including cancer, cardiovascular and neurodegenerative disease. Biogerontology research is well positioned to help prevent or at least postpone these diseases by identifying strategies to delay aging and altering its effects on macromolecular, cellular and extracellular damage so that the degree and type of damage does not reach the threshold required for disease incidence or progression. In Project 1 renewal application, we will study the effects of prolonged fasting cycles (PFC), fasting mimicking diet (FMD) cycles and protein restriction cycles (PRC) and of the GH-IGF-1 axis on the aging of the immune and nervous systems with focus on cellular protection and regeneration/rejuvenation. We propose to improve the fasting-mimicking dietary interventions shown in the previous funding period to promote healthspan and test the effect of bi-monthly cycles of these diets on healthspan in different genetic backgrounds. A central goal of Project 1 will be to identify periodic dietary interventions that extend healthspan without promoting adverse effects at very old ages. A major effort will be devoted to the identification of the molecular mechanisms responsible for the effects of periodic fasting mimicking diets on cellular protection with emphasis on the connection between nutrient signaling, stress resistance transcription factors, and the activation of a protective ketone body-activated alternative metabolic mode. Because of the focus of Projects 2 and 3 on mitochondria and stress resistance, we anticipate synergism between Project 1 and Project 2, which will investigate the effects and mechanisms of action of the DR mimicking mitochondrial peptide humanin (Project 2), and Project 3, which will test the hypothesis that the gas H2S is a central mediator of fasting- depended protection. Finally, based on our preliminary results showing that prolonged fasting increases stem cell-based regeneration in multiple systems, approximately half of the effort of Project 1, will be devoted to understanding the effect of periodic fasting and fasting mimicking diets on the regeneration of hematopoietic and neural stem cells and to the mechanisms underlying these effects. A key question that will be investigated is whether this regeneration results in a functional rejuvenation of the immune and nervous systems. We anticipate that the new insights gained from this project will continue to be translated into clinical trials to identify interventions that are safe and effective in improving human healthspan.

Public Health Relevance

We propose to study the molecular mechanisms linking nutrients to cellular protection and stem cell-based regeneration. We will investigate the effects and mechanism-of-action of periodic dietary restriction (prolonged fasting, fasting mimicking diet and protein restriction) and of inhibition of GHR/IGF-1 signaling in cellular protection, multi-system regeneration and age-related diseases. These studies will contribute to the identification of drugs and dietary interventions to treat but also prevent multiple diseases of aging by acting on the aging process and promoting multi-system rejuvenation.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Program Projects (P01)
Project #
2P01AG034906-06A1
Application #
9074574
Study Section
Special Emphasis Panel (ZAG1-ZIJ-2 (J2))
Project Start
2009-12-01
Project End
2017-07-31
Budget Start
2016-03-01
Budget End
2017-02-28
Support Year
6
Fiscal Year
2016
Total Cost
$293,005
Indirect Cost
$104,650
Name
University of Southern California
Department
Type
DUNS #
072933393
City
Los Angeles
State
CA
Country
United States
Zip Code
90032
Mao, Kai; Quipildor, Gabriela Farias; Tabrizian, Tahmineh et al. (2018) Late-life targeting of the IGF-1 receptor improves healthspan and lifespan in female mice. Nat Commun 9:2394
Kim, Su-Jeong; Mehta, Hemal H; Wan, Junxiang et al. (2018) Mitochondrial peptides modulate mitochondrial function during cellular senescence. Aging (Albany NY) 10:1239-1256
Xiao, Jialin; Cohen, Pinchas; Stern, Mariana Carla et al. (2018) Mitochondrial biology and prostate cancer ethnic disparity. Carcinogenesis 39:1311-1319
Nencioni, Alessio; Caffa, Irene; Cortellino, Salvatore et al. (2018) Fasting and cancer: molecular mechanisms and clinical application. Nat Rev Cancer 18:707-719
Qin, Qing; Delrio, Silvia; Wan, Junxiang et al. (2018) Downregulation of circulating MOTS-c levels in patients with coronary endothelial dysfunction. Int J Cardiol 254:23-27
Guidi, Novella; Longo, Valter D (2018) Periodic fasting starves cisplatin-resistant cancers to death. EMBO J 37:
Buono, Roberta; Longo, Valter D (2018) Starvation, Stress Resistance, and Cancer. Trends Endocrinol Metab 29:271-280
Qin, Qing; Mehta, Hemal; Yen, Kelvin et al. (2018) Chronic treatment with the mitochondrial peptide humanin prevents age-related myocardial fibrosis in mice. Am J Physiol Heart Circ Physiol 315:H1127-H1136
Hine, Christopher; Kim, Hyo-Jeong; Zhu, Yan et al. (2017) Hypothalamic-Pituitary Axis Regulates Hydrogen Sulfide Production. Cell Metab 25:1320-1333.e5
Nashiro, Kaoru; Guevara-Aguirre, Jaime; Braskie, Meredith N et al. (2017) Brain Structure and Function Associated with Younger Adults in Growth Hormone Receptor-Deficient Humans. J Neurosci 37:1696-1707

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