# Modulation of aging through mechanisms of nutrient demand and reward > **NIH NIH R37** · UNIVERSITY OF MICHIGAN AT ANN ARBOR · 2024 · $377,536 ## Abstract Project Summary Unrelenting growth in the number of elderly in our society and the resulting impact on the prevalence of age-related disease will have dramatic economic and health-related consequences over the next two decades. Although the causes and consequences of many diseases, including cancer and dementia, are slowly being unraveled, the mechanisms that underlie advanced age as the most significant risk factor associated with these disease states are relatively unknown. This is an important issue because single interventions that impact mechanisms of aging would be expected to ameliorate or eliminate multiple pathologies and diseases. We are, therefore, not just talking about extending lifespan; advances in understanding the basic biology of aging would have tremendous general health benefits as well. Our understanding of mammalian aging has been greatly stimulated over the past decade by research in simple model systems. Arguably, today’s most effective aging-related interventions in mice target sirtuin genes, as well as TOR and insulin/IGF signaling pathways, all of which were first identified in Saccharomyces cerevisiae, Caenorhabditis elegans, and Drosophila melanogaster. In recent years, molecular neuroscience, often using simple model organisms like Drosophila, has provided a well-defined framework for dissecting the causes and consequences of motivated behaviors. Homeostatic drives are as influential in this process as are rewarding experiences, and the neurons and neural circuits that influence motivation for foraging, mating, and many other behaviors also affect cellular pathways throughout the body, even those thought to be largely cell-autonomous. We have evidence that the circuits and neural states that encode feeding motivations are important modulators of aging. More specifically, our hypothesis is that specific mechanisms that evaluate internal and external nutrient availability and initiate physiological changes associated with states such as hunger and satiety play important roles in the modulation of behavior and lifespan. Harnessing the neurobiology of simple model systems to study the impact of how physiological decisions are made in response to evaluated energy status will yield insights into the broad influence of nutrients on longevity across taxa, including humans. It will also provide an understanding of the molecular details about how neuronal inputs orchestrate cell-autonomous and non-autonomous mechanisms to insure survival and health in a complex organism. The innovative nature of this proposal, which derives from the uniquely appropriate tools available in Drosophila together with a novel perspective about the importance of evaluative and motivational neural circuits on lifespan, provides the creativity and experimental power to develop and test hypotheses about the cell non-autonomous control of aging that have not been previously considered. In addition to providing an opportunity to discover basic mechani... ## Key facts - **NIH application ID:** 10849934 - **Project number:** 5R37AG051649-09 - **Recipient organization:** UNIVERSITY OF MICHIGAN AT ANN ARBOR - **Principal Investigator:** SCOTT PLETCHER - **Activity code:** R37 (R01, R21, SBIR, etc.) - **Funding institute:** NIH - **Fiscal year:** 2024 - **Award amount:** $377,536 - **Award type:** 5 - **Project period:** 2021-09-01 → 2026-05-31 ## Primary source NIH RePORTER: https://reporter.nih.gov/project-details/10849934 ## Citation > US National Institutes of Health, RePORTER application 10849934, Modulation of aging through mechanisms of nutrient demand and reward (5R37AG051649-09). Retrieved via AI Analytics 2026-05-23 from https://api.ai-analytics.org/grant/nih/10849934. Licensed CC0. --- *[NIH grants dataset](/datasets/nih-grants) · CC0 1.0*