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RF1AG095193

Project Grant

Overview

Grant Description
HUMAN NEUROPEPTIDE TRANSMITTER SYSTEMS ARE DYSREGULATED IN ALZHEIMER'S DISEASE PATHOGENESIS - PROJECT SUMMARY DIVERSE BRAIN NEUROPEPTIDES, KNOWN AS NEUROPEPTIDOMES, COMPRISE THE MAJORITY OF NEUROTRANSMITTERS THAT ARE ESSENTIAL FOR MODULATING ALZHEIMER’S DISEASE (AD) DEFICITS IN DEMENTIA. THE GAP IN THE FIELD IS THAT GLOBAL, UNBIASED NEUROPEPTIDOMICS ANALYSIS OF THE REPERTOIRE OF HUMAN BRAIN NEUROPEPTIDES HAS NOT YET BEEN ACHIEVED, NOR HAVE THE HUMAN BRAIN PROTEASES THAT PRODUCE NEUROPEPTIDES FROM THEIR PRECURSORS BEEN EXPERIMENTALLY IDENTIFIED. THEREFORE, THIS PROJECT WILL CLOSE THIS GAP BY DEFINING HUMAN BRAIN NEUROPEPTIDOMES AND THEIR BIOSYNTHETIC PROTEASES IN NORMAL AND AD CONDITIONS. IN SUPPORT OF THIS RESEARCH, OUR GROUP CONDUCTED A PILOT STUDY THAT DEMONSTRATES DYSREGULATION OF SYNAPTIC NEUROPEPTIDOMES IN HUMAN ALZHEIMER’S DISEASE (AD) BRAIN CORTEX COMPARED TO AGE-MATCHED CONTROLS, INVOLVING PROTEOLYTIC MECHANISMS. FURTHERMORE, TO IDENTIFY PROTEASES UTILIZED TO SYNTHESIZE NEUROPEPTIDOME COMPONENTS, WE DEVELOPED A MULTI-OMICS APPROACH WHICH INTEGRATES NEUROPEPTIDOMICS, PROTEASE CLEAVAGE PROFILING, AND PROTEOMICS. GIVEN THAT HUMAN-SPECIFIC MECHANISMS FOR NEUROPEPTIDE PRODUCTION MAY EXIST, STUDIES OF HUMAN BRAIN NEUROPEPTIDOMES ARE NECESSARY TO UNDERSTAND NEUROTRANSMITTER REGULATION IN NORMAL HUMAN BRAIN AND IN HUMAN AD BRAIN. THE GOALS OF THIS PROJECT WILL BE TO, FIRSTLY, ELUCIDATE THE FULL REPERTOIRE OF NEUROPEPTIDOME SIGNATURES AND THEIR BIOSYNTHETIC PROTEASES IN NORMAL HUMAN BRAIN HIPPOCAMPUS AND CORTEX SUBREGIONS THAT PARTICIPATE IN MEMORY FUNCTIONS, COMBINED WITH THE HYPOTHALAMUS THAT REGULATES METABOLISM AND STRESS. SECONDLY, HUMAN BRAIN REGIONS FROM AD AND THE PRE-AD STAGE OF MILD COGNITIVE IMPAIRMENT (MCI) WILL BE ASSESSED FOR DYSREGULATION OF NEUROPEPTIDOMES AND BIOSYNTHETIC PROTEASES COMPARED TO AGE-MATCHED CONTROLS. DYSREGULATED NEUROPEPTIDES, INCLUDING THE CHROMOGRANINS AND VGF, WILL BE ASSESSED FOR REGULATING NEURONAL ACTIVITIES AND TOXICITIES. WE WILL ASSESS THE HYPOTHESIS THAT SYNAPTIC NEUROPEPTIDOMES ARE DYSREGULATED IN HUMAN AD BRAIN, AND THAT THEY POSSESS BIOLOGICAL ACTIVITIES FOR REGULATING NEURONAL FUNCTIONS. THE SPECIFIC AIMS WILL (1) STUDY NORMAL HUMAN BRAIN REGIONS INVOLVED IN MEMORY FUNCTION TO DEFINE NEUROPEPTIDOMES AND THEIR BIOSYNTHETIC PROTEASES BY MULTI- OMICS STRATEGIES, (2) EVALUATE PROTEASE PRODUCTION OF HUMAN NEUROPEPTIDOMES IN YOUNG TO OLDER AGES OF HUMAN INDUCED NEURONS (INS), (3) INVESTIGATE HUMAN AD AND MCI BRAINS FOR DYSREGULATED SYNAPTIC NEUROPEPTIDOMES AND THEIR BIOSYNTHETIC PROTEASES COMPARED TO CONTROLS, AND (4) CONDUCT FUNCTIONAL ANALYSIS OF AD DYSREGULATED NEUROPEPTIDES FOR REGULATING NEURONAL ELECTRICAL NETWORK ACTIVITY, METABOLISM, INFLAMMATION, CELL DEATH, AND MOLECULAR PATHWAYS OF CELLULAR FUNCTIONS IN HUMAN SPORADIC AD, MCI, AND AGE-MATCHED INS. SIGNIFICANT FINDINGS WILL DISCOVER NORMAL BRAIN NEUROPEPTIDES AND THEIR BIOSYNTHETIC PROTEASE MECHANISMS, AND, IMPORTANTLY, PROVIDE NEW KNOWLEDGE OF DYSREGULATED HUMAN BRAIN AD NEUROPEPTIDOMES THAT REGULATE NEURONAL DEFICITS RELATED TO AD. SUCH NEUROPEPTIDES MAY REPRESENT NOVEL AD BIOMARKERS, AND BIOSYNTHETIC PROTEASES MAY REPRESENT NEW DRUG TARGETS FOR FUTURE AD DRUG DISCOVERY.
Funding Goals
TO ENCOURAGE BIOMEDICAL, SOCIAL, AND BEHAVIORAL RESEARCH AND RESEARCH TRAINING DIRECTED TOWARD GREATER UNDERSTANDING OF THE AGING PROCESS AND THE DISEASES, SPECIAL PROBLEMS, AND NEEDS OF PEOPLE AS THEY AGE. THE NATIONAL INSTITUTE ON AGING HAS ESTABLISHED PROGRAMS TO PURSUE THESE GOALS. THE DIVISION OF AGING BIOLOGY EMPHASIZES UNDERSTANDING THE BASIC BIOLOGICAL PROCESSES OF AGING. THE DIVISION OF GERIATRICS AND CLINICAL GERONTOLOGY SUPPORTS RESEARCH TO IMPROVE THE ABILITIES OF HEALTH CARE PRACTITIONERS TO RESPOND TO THE DISEASES AND OTHER CLINICAL PROBLEMS OF OLDER PEOPLE. THE DIVISION OF BEHAVIORAL AND SOCIAL RESEARCH SUPPORTS RESEARCH THAT WILL LEAD TO GREATER UNDERSTANDING OF THE SOCIAL, CULTURAL, ECONOMIC AND PSYCHOLOGICAL FACTORS THAT AFFECT BOTH THE PROCESS OF GROWING OLD AND THE PLACE OF OLDER PEOPLE IN SOCIETY. THE DIVISION OF NEUROSCIENCE FOSTERS RESEARCH CONCERNED WITH THE AGE-RELATED CHANGES IN THE NERVOUS SYSTEM AS WELL AS THE RELATED SENSORY, PERCEPTUAL, AND COGNITIVE PROCESSES ASSOCIATED WITH AGING AND HAS A SPECIAL EMPHASIS ON ALZHEIMER'S DISEASE. SMALL BUSINESS INNOVATION RESEARCH (SBIR) PROGRAM: TO EXPAND AND IMPROVE THE SBIR PROGRAM, TO INCREASE PRIVATE SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL RESEARCH AND DEVELOPMENT, TO INCREASE SMALL BUSINESS PARTICIPATION IN FEDERAL RESEARCH AND DEVELOPMENT, AND TO FOSTER AND ENCOURAGE PARTICIPATION OF SOCIALLY AND ECONOMICALLY DISADVANTAGED SMALL BUSINESS CONCERNS AND WOMEN-OWNED SMALL BUSINESS CONCERNS IN TECHNOLOGICAL INNOVATION. SMALL BUSINESS TECHNOLOGY TRANSFER (STTR) PROGRAM: TO STIMULATE AND FOSTER SCIENTIFIC AND TECHNOLOGICAL INNOVATION THROUGH COOPERATIVE RESEARCH DEVELOPMENT CARRIED OUT BETWEEN SMALL BUSINESS CONCERNS AND RESEARCH INSTITUTIONS, TO FOSTER TECHNOLOGY TRANSFER BETWEEN SMALL BUSINESS CONCERNS AND RESEARCH INSTITUTIONS, TO INCREASE PRIVATE SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL RESEARCH AND DEVELOPMENT, AND TO FOSTER AND ENCOURAGE PARTICIPATION OF SOCIALLY AND ECONOMICALLY DISADVANTAGED SMALL BUSINESS CONCERNS AND WOMEN-OWNED SMALL BUSINESS CONCERNS IN TECHNOLOGICAL INNOVATION.
Grant Program (CFDA)
Place of Performance
California United States
Geographic Scope
State-Wide
San Diego University Of California was awarded Human Brain Neuropeptide Dysregulation in Alzheimer's Disease Project Grant RF1AG095193 worth $3,138,871 from National Institute on Aging in September 2025 with work to be completed primarily in California United States. The grant has a duration of 4 years and was awarded through assistance program 93.866 Aging Research. The Project Grant was awarded through grant opportunity NIH Research Project Grant (Parent R01 Clinical Trial Not Allowed).

Status
(Ongoing)

Last Modified 9/24/25

Period of Performance
9/15/25
Start Date
8/31/29
End Date
1.0% Complete

Funding Split
$3.1M
Federal Obligation
$0.0
Non-Federal Obligation
$3.1M
Total Obligated
100.0% Federal Funding
0.0% Non-Federal Funding

Activity Timeline

Interactive chart of timeline of amendments to RF1AG095193

Additional Detail

Award ID FAIN
RF1AG095193
SAI Number
RF1AG095193-43499630
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Public/State Controlled Institution Of Higher Education
Awarding Office
75NN00 NIH National Insitute on Aging
Funding Office
75NN00 NIH National Insitute on Aging
Awardee UEI
UYTTZT6G9DT1
Awardee CAGE
50854
Performance District
CA-90
Senators
Dianne Feinstein
Alejandro Padilla
Modified: 9/24/25