Sexually-Dimorphic Regulation of Sleep

Information

  • Research Project
  • 10210453
  • ApplicationId
    10210453
  • Core Project Number
    R01NS109151
  • Full Project Number
    5R01NS109151-04
  • Serial Number
    109151
  • FOA Number
    PA-18-484
  • Sub Project Id
  • Project Start Date
    9/17/2018 - 5 years ago
  • Project End Date
    7/31/2023 - 10 months ago
  • Program Officer Name
    HE, JANET
  • Budget Start Date
    8/1/2021 - 2 years ago
  • Budget End Date
    7/31/2022 - a year ago
  • Fiscal Year
    2021
  • Support Year
    04
  • Suffix
  • Award Notice Date
    8/26/2021 - 2 years ago

Sexually-Dimorphic Regulation of Sleep

Sleep is essential for healthy mind and body. It is regulated by homeostasis, by which accumulated sleep drive during wakefulness leads to increased propensity toward sleep. However, we can stay up late if we have something important or interesting to do, for example, take care of a baby or read a fascinating book. In other words, sleep is also regulated by motivational states. Thus sleep drive competes with other motivational drives to decide whether we sleep or engage in other important or interesting activities. We have recently shown that sex drive profoundly affects male sleep in Drosophila and that a subset of octopaminergic neurons (octopamine is analogous to human norepinephrine) mediates sleep suppression by male sex drive. Previous studies have shown that female flies sleep less and lay more eggs after mating. Thus both males and females adjust their sleep patterns to meet reproductive needs. However, the neural mechanisms of how sleep and reproductive behaviors are balanced are not well understood. In preliminary studies for this proposal, we identified several previously uncharacterized neuronal populations for balancing sleep and reproductive behaviors in males and females. Two of the newly identified populations are dopaminergic, suggesting that octopamine and dopamine signaling pathways cooperate to integrate sleep and reproductive behaviors. We will determine the anatomical and physiological connectivity among the various neuronal populations, and investigate their role in sleep and reproductive behaviors using a combination of behavioral analysis, calcium imaging, circuit tracing, immunohistochemistry, and generation of new drivers for precise manipulation of specific neurons. Our proposed studies offer an excellent opportunity to discover basic neural mechanisms and general organizing principles that underlie the balance between competing drives. Investigating how sleep regulatory mechanisms communicate with neural mechanisms for sexually-dimorphic behaviors using neuromodulators such as octopamine and dopamine may lead to a better understanding of how the human brain integrates sleep drive and other motivational states.

IC Name
NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE
  • Activity
    R01
  • Administering IC
    NS
  • Application Type
    5
  • Direct Cost Amount
    218750
  • Indirect Cost Amount
    122500
  • Total Cost
    341250
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    853
  • Ed Inst. Type
    SCHOOLS OF MEDICINE
  • Funding ICs
    NINDS:341250\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    NNRS
  • Study Section Name
    Neuroendocrinology, Neuroimmunology, Rhythms and Sleep Study Section
  • Organization Name
    THOMAS JEFFERSON UNIVERSITY
  • Organization Department
    NEUROSCIENCES
  • Organization DUNS
    053284659
  • Organization City
    PHILADELPHIA
  • Organization State
    PA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    191074418
  • Organization District
    UNITED STATES