# Integrative Neuroscience Initiative on Alcoholism

> **NIH NIH U24** · UNIVERSITY OF TEXAS AT AUSTIN · 2021 · $481,012

## Abstract

PROJECT SUMMARY
This is a competing renewal application for the Integrative Neuroscience Initiative on Alcoholism (INIA)-
Neuroimmune consortium (Notice# RFA-AA-16-004/005/006) to identify drug targets based on the genomic,
cellular, and behavioral neuroadaptations related to excessive alcohol consumption. INIA-Neuroimmune (INIA-
N) will address several NIAAA goals, including: 1) understanding the genomics, electrophysiology, and
pharmacology of brain immune pathways and their role in alcohol use disorders (AUDs); 2) using new
technologies to study neural circuits involved in excessive alcohol drinking; 3) promoting data reproducibility
and translation through testing in multiple species (including humans), multiple laboratories, and multiple
assays; 4) using emerging computational resources that connect gene networks to drugs to identify
compounds with potential to reduce excessive drinking. A key goal for INIA-N is to probe cross-species
genomic datasets, together with novel computational approaches, to predict FDA-approved drugs that can be
repurposed to treat AUDs. The overall hypothesis for INIA-N is that excessive alcohol consumption causes
genetic changes and neuroadaptations in immune-related pathways that are conserved across multiple
species (including humans), allowing for the systematic selection and testing of drug targets from the
computational to the clinical level. Ten Research Components, two Scientific Cores, and an Administrative
Core comprise the consortium. INIA-N will be directed by the Administrative Core in cooperation with the
Executive and Steering Committees and guided by a distinguished Scientific Advisory Board. The
Administrative Core will provide leadership, oversight of scientific projects, authentication of study drugs, and
integration and translation of project data. INIA-N has four goals: 1) Expand our rodent and human genomic
studies to include non-human primates (in collaboration with INIA-Stress) and new rodent models, and
integrate these with existing datasets. We will also integrate genetic (genome-wide association studies) and
genomic analyses (new human RNA-Seq datasets) to facilitate drug target identification, with an emphasis on
neuroimmune targets and the unexplored role of novel non-coding RNAs and splice variants in alcohol
consumption; 2) Combine extensive genomic resources with new computational approaches to identify
candidate drugs that may be repurposed to treat AUDs. These drugs will be tested in several animal drinking
models; 3) Apply systems-level approaches (electrophysiology and live brain imaging) to understand how
excessive drinking changes brain function, with an emphasis on our top neuroimmune targets; 4) Select
leading candidates that emerge from rigorous behavioral and functional testing to study in the new human
laboratory component. INIA-N research encompasses a unique `gene network to pharmacotherapy' approach
to apply cutting-edge computational tools to nominate gene targets and...

## Key facts

- **NIH application ID:** 10087453
- **Project number:** 5U24AA025479-05
- **Recipient organization:** UNIVERSITY OF TEXAS AT AUSTIN
- **Principal Investigator:** Robert A Harris
- **Activity code:** U24 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2021
- **Award amount:** $481,012
- **Award type:** 5
- **Project period:** 2017-02-01 → 2022-01-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10087453

## Citation

> US National Institutes of Health, RePORTER application 10087453, Integrative Neuroscience Initiative on Alcoholism (5U24AA025479-05). Retrieved via AI Analytics 2026-05-23 from https://api.ai-analytics.org/grant/nih/10087453. Licensed CC0.

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