Multidisciplinary Characterization of the Gut-Brain Axis in Addiction
Project Number1DP2AT013279-01
Former Number1DP2OD036582-01
Contact PI/Project LeaderCUESTA, SANTIAGO
Awardee OrganizationRUTGERS, THE STATE UNIV OF N.J.
Description
Abstract Text
Project Summary
Addiction and substance use disorders (SUDs) affect more than 27 million people in the United States,
with an estimated $740 billion annual cost due to crime, lost work productivity, and health care expenses.
Unfortunately, these numbers continue to increase and even more, since the pandemic, unleashing an alarming
health and social burden. Despite worldwide efforts, no successful treatments have been developed to better
deal with this chronic and relapsing disease. In the past years, the gut microbiota and its composition has been
associated with different adult behaviors and diverse neuropsychological diseases, including SUDs. However,
the mechanism by which the gut microbiota influences these pathologies remains elusive, with most of the
available data originating from associations between human patients or animal models and their fecal
microbiome profiles. There is an urgent need to push the field toward more mechanistic studies to find actual
communication pathways and molecular mediators behind these gut-brain connections. Therefore, the goal of
this project is to identify and characterize relevant interactions between different members of the gut microbiota,
psychostimulant exposure, and vulnerability to develop SUDs. To this end, we will apply a conceptually and
technically innovative approach that really bridges the fields of neuroscience and microbiology. We will use
metagenomics and metabolomics to identify psychostimulant-induced alteration in microbial composition and
gut milieu. We will then apply pharmacological and microbiological techniques to modulate gut physiology and
bacterial genetics to validate identified host signals and characterize bacteria-sensing pathways that are
impacted by the drug. To understand how the microbiome influences the progression to disease, we will combine
gut microbial manipulations with well-established animal models to determine the impact of these manipulations
on addiction. We will leverage the availability of genetically tractable hosts (mice) and human gut bacterial strains
to build up in vitro and in vivo models that will allow us to better understand the molecular mechanisms involved
in this interkingdom communication. This project is only possible because we have developed the protocols and
the technical resources to accurately manipulate and investigate bacterial physiology while also following
neurobehavioral alterations associated with psychiatric diseases. We have the experience and the equipment to
run a battery of behavioral tests under microbiologically controlled conditions. Our approach provides an exciting
opportunity for acquiring new knowledge regarding addiction, gut microbiome physiology, and their interaction,
that can make a vertical leap in the field.
|Contact PD/PI: Cuesta, Santiago
Public Health Relevance Statement
PROJECT NARRATIVE
Addiction is a chronic, relapsing disorder that affects millions of people in the United States and worldwide, and
yet no successful treatments have been developed. In the past years, the composition and type of bacteria that
inhabit our gut (the gut microbiota) has emerged as a crucial regulator of brain maturation, function, and response
to different diseases, including addiction; however, the mechanisms behind this communication remain mostly
unknown. This project proposes a novel multidisciplinary approach directed to characterize clear and
mechanistically defined interactions between the gut microbiota, psychostimulant use, and addiction, which can
lead to the development of more successful evidence-based systemic interventions for treating this debilitating
psychopathology.
|Contact PD/PI: Cuesta, Santiago
National Center for Complementary and Integrative Health
CFDA Code
310
DUNS Number
001912864
UEI
M1LVPE5GLSD9
Project Start Date
17-September-2024
Project End Date
31-August-2027
Budget Start Date
17-September-2024
Budget End Date
31-August-2027
Project Funding Information for 2024
Total Funding
$1,391,376
Direct Costs
$900,000
Indirect Costs
$491,376
Year
Funding IC
FY Total Cost by IC
2024
NIH Office of the Director
$1,391,376
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 1DP2AT013279-01
Publications
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Outcomes
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Clinical Studies
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