# Nicotinic receptors and alcohol reinforcement

> **NIH NIH R01** · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · 2020 · $381,375

## Abstract

PROJECT SUMMARY
This application is submitted in response to PA-13-194: Mechanisms of alcohol and nicotine co-addiction.
Allelic variation in CHRNA5, the gene encoding the α5 nicotinic acetylcholine receptor (nAChR) subunit,
increases vulnerability to alcohol and tobacco dependence. Here, we will use cutting-edge molecular, genetic
and behavioral techniques to investigate the role for α5* nAChRs, particularly those in the medial habenula
(MHb)-interpeduncular nucleus (IPN) pathway where α5* nAChRs are densely expressed, in regulating the
motivational properties of alcohol. In Specific Aim I, we will assess alcohol drinking in two lines of mice with
deficient α5* nAChR signaling: α5 subunit knockout mice and “humanized” knock-in mice in which the α5
nAChR subunit gene has been genetically modified to express the major risk allele for tobacco and alcohol
dependence in humans. Second, we will use the intracranial self-stimulation (ICSS) procedure to assess the
rewarding and aversive effects of alcohol in these lines of mutant mice. We predict that alcohol intake will be
increased, and aversive effects of alcohol decreased, in mice with deficient α5* nAChR signaling. In Specific
Aim II, we will investigate the effects of alcohol on the MHb-IPN system. First, we will use optogenetics coupled
with electrophysiological recordings to examine the effects of alcohol on excitatory and inhibitory transmission
at the MHb-IPN synapse and determine the role for α5* nAChRs in these effects. Second, we will use rubidium
efflux assays to determine the effects of alcohol drinking on the activity of α5* nAChRs in the MHb-IPN system.
We predict that alcohol stimulates excitatory MHb inputs to IPN – an “aversion” signal – and that this effect is
attenuated by deficient α5* nAChR signaling. We further predict that prolonged alcohol intake results in
diminished activity of α5* nAChRs in MHb-IPN system, which may contribute to the development of the alcohol
drinking habit. In Specific Aim III, we will investigate the involvement of the MHb-IPN system, and α5* nAChRs
in this system, in regulating alcohol drinking. First, we will use an elegant Cre recombinase-dependent
chemogenetics (DREADD) approach to stimulate or inhibit neurons in the MHb-IPN system, or more
selectively only those MHb-IPN neurons that express α5* nAChRs, and examine effects on alcohol drinking.
Second, we will use virus-mediated gene transfer to re-express otherwise absent α5 nAChR subunits in MHb
or IPN neurons of the α5 KO mice and examine the effects on alcohol drinking in these mice. We predict that
the MHb-IPN system, and α5* nAChRs in this system, play a key role in regulating alcohol intake. This
innovative program of research may yield novel insights into the mechanisms of alcohol dependence that
supports development of entirely new classes of therapeutic agents.

## Key facts

- **NIH application ID:** 9905468
- **Project number:** 5R01AA024292-05
- **Recipient organization:** ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI
- **Principal Investigator:** Paul J. Kenny
- **Activity code:** R01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2020
- **Award amount:** $381,375
- **Award type:** 5
- **Project period:** 2016-07-15 → 2021-03-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/9905468

## Citation

> US National Institutes of Health, RePORTER application 9905468, Nicotinic receptors and alcohol reinforcement (5R01AA024292-05). Retrieved via AI Analytics 2026-05-26 from https://api.ai-analytics.org/grant/nih/9905468. Licensed CC0.

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