# Impact of chronic, voluntary fentanyl intake on single-cell gene expression and brain-wide neuronal activity patterns

> **NIH NIH F30** · UNIVERSITY OF WASHINGTON · 2024 · $44,942

## Abstract

Abstract/Project Summary
 Opioid use disorder is defined as chronic, maladaptive opioid use despite negative consequences.
Prolonged opioid exposure can induce long-lasting changes to neural circuitry involved with reward and
motivation, leading to drug cravings and tolerance to the drug’s rewarding effects over time. One brain region
known to play a key role in opioid reward processing is the nucleus accumbens, which contains two
subpopulations of GABAergic medium spiny neurons that express either the D1 or D2 dopamine receptor, as
well as a variety of interneuron cell types and glia. Medium spiny neurons project to multiple brain regions, and
µ-opioid receptors are also expressed on many neurons throughout the brain. Thus, it is reasonable to predict
that chronic opioid exposure will be associated with global alterations in neuronal activity patterns. Improving
our understanding of both the molecular and circuit-level mechanisms underlying opioid use disorder is crucial
to facilitating the development of more effective treatments.
 To address this gap in knowledge, I plan to leverage a rodent model of chronic, voluntary oral fentanyl
intake that I have developed and implemented. My goal for this training proposal is to use this paradigm to
specifically assess what changes occur to gene expression and neural circuitry over periods of sustained
opioid self-administration. In Aim 1, we plan to conduct single nuclei RNAseq in the nucleus accumbens of
mice after chronic fentanyl intake and withdrawal. Aim 2 will utilize transgenic mice to visualize expression of
the early immediate gene cFOS, a marker of neuron activity. Whole-brain clearing and light-sheet microscopy
will be used to quantify the neural activation patterns associated with long-term fentanyl escalation and
withdrawal. Together, these aims will lead to a more complete understanding of the impact of chronic opioid
exposure, which may inform the development of novel therapeutic interventions for opioid use disorder.

## Key facts

- **NIH application ID:** 10994005
- **Project number:** 1F30DA061559-01
- **Recipient organization:** UNIVERSITY OF WASHINGTON
- **Principal Investigator:** Cassidy Taylor Burke
- **Activity code:** F30 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2024
- **Award amount:** $44,942
- **Award type:** 1
- **Project period:** 2024-08-01 → 2027-07-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10994005

## Citation

> US National Institutes of Health, RePORTER application 10994005, Impact of chronic, voluntary fentanyl intake on single-cell gene expression and brain-wide neuronal activity patterns (1F30DA061559-01). Retrieved via AI Analytics 2026-05-24 from https://api.ai-analytics.org/grant/nih/10994005. Licensed CC0.

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