Mechanism of action of gastric Interstitial cells of Cajal

Information

  • Research Project
  • 10263376
  • ApplicationId
    10263376
  • Core Project Number
    R01DK057236
  • Full Project Number
    5R01DK057236-15
  • Serial Number
    057236
  • FOA Number
    PA-19-056
  • Sub Project Id
  • Project Start Date
    9/1/2000 - 24 years ago
  • Project End Date
    7/31/2023 - a year ago
  • Program Officer Name
    HAMILTON, FRANK A
  • Budget Start Date
    8/1/2021 - 3 years ago
  • Budget End Date
    7/31/2022 - 2 years ago
  • Fiscal Year
    2021
  • Support Year
    15
  • Suffix
  • Award Notice Date
    8/19/2021 - 3 years ago

Mechanism of action of gastric Interstitial cells of Cajal

Summary The stomach is a miraculous organ that can accept large volumes of food and then grind up solids to make nutrients absorbable in the small intestine. Unfortunately some patients find eating, a palpable joy of living, an uncomfortable or painful experience. Functional disorders of gastric motility plague the lives of these patients and therapies are out of reach because the basic mechanisms of gastric motility are unknown. New techniques allow monitoring of the pacemaker activity that fuels gastric peristalsis and gastric emptying, and this project proposes to utilize cutting-edge approaches to better understand basic mechanisms of gastric motility. Three specific aims will be pursued: i) Characterize the relationship between Ca2+ signaling patterns and pacemaker activity in interstitial cells of Cajal (ICC-MY and ICC-IM) of the mouse and human gastric corpus and antrum; ii) Compare molecular and functional characteristics of the pacemakersomes in mouse and human corpus and aims will investigate the basic cellular behaviors that generate pacemaker activity ICC-MY and ICC-IM using optogenetic and electrophysiological techniques to monitor pacemaker activity of ICC in situ. Preliminary data suggest that Ca2+ transients underlie the electrical responses known as slow waves that power gastric peristalsis. The basis for the corpus-to-antrum frequency gradient will be explored and concepts about why corpus frequency exceeds antral frequency will be investigated. The basis for propagation of slow waves in ICC networks will be investigated and the mechanisms responsible for integrated organization of pacemaker activity will be determined. Optogenetics provides the opportunity to study the pattern of ICC activation in intact gastric muscles and the intact stomach. Preliminary data reveals a novel pattern of slow wave activation never previously observed with extracellular electrical recording. We will also investigate how enteric motor neural inputs and other chronotropic mediators regulate gastric slow waves and how application of chronotropic stimuli affects the pattern of slow wave propagation in the stomach. OMB No. 0925-0001/0002 (Rev. 01/18 Approved Through 03/31/2020)Page Continuation Format Page

IC Name
NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES
  • Activity
    R01
  • Administering IC
    DK
  • Application Type
    5
  • Direct Cost Amount
    354063
  • Indirect Cost Amount
    155788
  • Total Cost
    509851
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    847
  • Ed Inst. Type
    SCHOOLS OF MEDICINE
  • Funding ICs
    NIDDK:509851\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    UNIVERSITY OF NEVADA RENO
  • Organization Department
    PHYSIOLOGY
  • Organization DUNS
    146515460
  • Organization City
    RENO
  • Organization State
    NV
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    89557
  • Organization District
    UNITED STATES