Pathogenic role of peroxisome proliferator-activated receptor alpha in periodontitis

Information

  • Research Project
  • 10108079
  • ApplicationId
    10108079
  • Core Project Number
    R03DE030209
  • Full Project Number
    1R03DE030209-01
  • Serial Number
    030209
  • FOA Number
    PAR-19-370
  • Sub Project Id
  • Project Start Date
    3/3/2021 - 3 years ago
  • Project End Date
    2/28/2023 - a year ago
  • Program Officer Name
    CHANDER, PREETHI
  • Budget Start Date
    3/3/2021 - 3 years ago
  • Budget End Date
    2/28/2022 - 2 years ago
  • Fiscal Year
    2021
  • Support Year
    01
  • Suffix
  • Award Notice Date
    3/3/2021 - 3 years ago
Organizations

Pathogenic role of peroxisome proliferator-activated receptor alpha in periodontitis

Project Summary Periodontitis is an important public health problem among adults in the U.S., with major economic costs for prevention and treatment and significant impact on quality of life. Un-controlled periodontitis can cause ex- tensive tooth loss, jaw bone deterioration, and increased risk of developing systemic diseases. Conventional treatments that rely on antibiotics and mechanical removal of dental plaque are transiently effective because they indirectly address the inflammation and related immune responses that underlie periodontitis, but do not directly impact pathogenesis. Thus, there is a compelling need to investigate novel target molecules which di- rectly modulate pathogenesis for both inflammation and bone loss in periodontitis. It has been demonstrated that PPAR? agonists (PPAR?A), which is PPAR? specific, have robust protective actions limiting inflammation in autoimmune disease, modulating inflammation. Our preliminary data suggest that a PPAR?A, fenofibrate, has the potential to reduce periodontal inflammation and bone resorption in experimental periodontitis mouse mod- els, suggesting that the pathological role of PPAR? in periodontitis deserves further investigation. We propose to test the hypothesis that PPAR? not PPAR? or PPAR? plays important pathological roles in periodontitis. To that end, two distinct but complementary specific aims are proposed. Aim1 will determine that PPAR? not PPAR? or PPAR? has expression level changes in periodontitis. Aim 2 will determine PPAR? Knockout or overexpres- sion will affect inflammation and bone loss in experimental periodontitis mouse model. The understanding of expression level change of PPAR? in periodontitis investigated during Aim1 will provide the foundation for Aim2. The goal is to reveal the role of PPAR? in inflammatory regulation and in modulation of bone homeostasis during periodontal diseases. Building on previous experience and both Aim1 and Aim2 will lead to the development of novel, PPAR? targeted therapies for periodontits and various other oral diseases. Successful completion of this project will lead to better understanding of the molecular and cellular role of PPAR? in periodontitis, and translate this knowledge to develop an application system to achieve sustained release with noninvasive local delivery for the clinical treatment of periodontitis.

IC Name
NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH
  • Activity
    R03
  • Administering IC
    DE
  • Application Type
    1
  • Direct Cost Amount
    100000
  • Indirect Cost Amount
    99000
  • Total Cost
    199000
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    121
  • Ed Inst. Type
  • Funding ICs
    NIDCR:199000\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    DSR
  • Study Section Name
    NIDR Special Grants Review Committee
  • Organization Name
    FORSYTH INSTITUTE
  • Organization Department
  • Organization DUNS
    062190616
  • Organization City
    CAMBRIDGE
  • Organization State
    MA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    021421200
  • Organization District
    UNITED STATES