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| Funder | NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES |
|---|---|
| Recipient Organization | Washington University |
| Country | United States |
| Start Date | Aug 20, 2024 |
| End Date | Jun 30, 2029 |
| Duration | 1,775 days |
| Number of Grantees | 1 |
| Roles | Principal Investigator |
| Data Source | NIH (US) |
| Grant ID | 10945850 |
Abstract Interstitial cystitis/bladder pain syndromes (IC/BPS) are a debilitating painful condition with unknown etiology. The cells and the circuits in the spinal cord that process non-noxious (bladder function) and noxious (intense bladder pressure or discomfort) sensory information from the bladder is not well established. What specific
roles different spinal anatomical substrates play in processing pathological bladder sensations and voiding dysfunction is unclear. In this proposal, we will test how distinct spinal cord cells that are activated by cystitis are necessary for maladaptive micturition and bladder nociception. We will use chemogenetics and
optogenetics approaches to determine the precise roles the cystitis activated spinal cord cells play micturition and bladder nociception. Furthermore, we will determine how this information is streamed to the distinct brain regions. Finally, we propose to perform molecular description of genetically classified spinal cell populations
using transcriptomics and fluorescent in situ hybridization. These studies will lead to a cellular and functional characterization of cystitis activated spinal cord cells and to a better understanding of how different symptoms of cystitis are regulated in the spinal cord. These efforts will advance our understanding of spinal circuits in
cystitis and may enable development of new therapeutic strategies for the treatment of IC/BPS.
Washington University
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