# CRCNS: Reward and motivation in neural networks

> **NIH NIH R01** · COLD SPRING HARBOR LABORATORY · 2020 · $432,000

## Abstract

The overall goal of this project is to develop a reinforcement learning (RL) theory of motivation, understood
here as motivational salience, and to test the conclusions of this theory using experimental observations
obtained in the ventral pallidum (VP). Animals' actions depend on the shifting values of internal demands
determined by physiological or behavioral conditions, such as thirst, hunger, addiction, specific nutrient
deficiency, etc. These need-based modulations of the perceived values of reinforcements (reward or
punishment} are described by a mathematical variable called motivational salience or, simply, motivation.
Including motivation adds a new level of complexity to RL theory, and allows it to generate flexible ongoing
behaviors. Here, we will investigate how motivation can be learned by neuronal networks to generate
complex adaptive behaviors and compare the conclusions of our theory with the VP circuits. Previous studies
indicate that the VP plays an important role in a variety of behaviors, potentially, by influencing motivational
salience. In vivo recordings suggest that VP neuron firing correlates with motivational states. Lesions,
pharmacological and optogenetic manipulations in VP cause profound changes in behaviors motivated by
natural rewards or drugs of addiction. Dysfunction of this structure is linked to depression and drug addiction
in humans. Our theoretical results suggest that distinct classes of neurons in the VP should play essential
roles in representing either positive or negative motivational states. We further hypothesize that the functional
interactions locally within the VP are critical for generating such signals that guide motivated behaviors.
Consistent with predictions of RL theory, in our preliminary studies, we found that individual VP neurons
could be classified as either positive or negative 'motivation neurons', as the activities of these neurons
represented both expected values of outcomes and motivational states. When population activity is
considered, representations of outcome expectation can be distinguished from representations of motivation
fluctuating according to the animals' physiological states. Based on the preliminary data, we devised an
integrated approach, combining studies in computational analysis and theory (Koulakov lab) with advanced
molecular genetic tools, optogenetics, chemogenetics, electrophysiology, and imaging in behaving mice (Li
lab), to test our hypotheses through the following Aims: Aim 1. To develop methods for identifying motivation
in the population activity of VP neurons. Here we will use novel behavioral and computational methods to
disambiguate representations of motivation and outcome expectation in neuronal responses. Aim 2. To
develop reinforcement learning theory of motivation and to test its predictions using responses of VP neurons.
Here we will develop the Q-learning theory of motivation and compare networks trained using this theory to
responses of VP neur...

## Key facts

- **NIH application ID:** 10017031
- **Project number:** 5R01DA050374-02
- **Recipient organization:** COLD SPRING HARBOR LABORATORY
- **Principal Investigator:** ALEXEI KOULAKOV
- **Activity code:** R01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2020
- **Award amount:** $432,000
- **Award type:** 5
- **Project period:** 2019-09-30 → 2024-07-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10017031

## Citation

> US National Institutes of Health, RePORTER application 10017031, CRCNS: Reward and motivation in neural networks (5R01DA050374-02). Retrieved via AI Analytics 2026-05-23 from https://api.ai-analytics.org/grant/nih/10017031. Licensed CC0.

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