# Molecular basis for adenosine A3 receptor agonists in the treatment of migraine

> **NIH NIH R01** · UNIVERSITY OF MARYLAND BALTIMORE · 2022 · $498,920

## Abstract

Project Summary/Abstract
Despite recent advances with new therapies, a huge proportion of migraine patients are still unable to use
established therapeutics. For many patients, treatments are not effective, even newly approved CGRP mAbs
have response rates of only ~50%. For others they are unsafe due to contraindications (triptans), or like opioids,
not suited for long term use, even exacerbating existing migraine headache. This illustrates that there are still
major gaps in our understanding of migraine mechanisms. It is therefore imperative that we investigate the
underlying molecular mechanisms involved, geared towards identifying novel therapeutic targets with potential
for rapid translation to the clinic. Recent data have identified the adenosine A3 receptor (A3AR) as a novel target
for pain. Our recent work has also established that production of the highly noxious reactive nitroxidative species,
peroxynitrite (PN), causes downstream modifications to glutamatergic signaling and NLRP3/IL-1β-driven
neuroinflammation, to mediate nociceptive spinal sensitization. We show that A3AR agonists attenuate these
nociceptive mechanisms in diverse rodent models of neuropathic pain, providing persistent pain relief. Despite
this, little is known about A3AR-PN mechanisms in trigeminovascular migraine models. However, our preliminary
data demonstrate that A3AR are expressed in important peripheral and central regions along the migraine pain
pathway, and A3AR agonists inhibit migraine-like responses in several rodent models of migraine that are highly
predictive of therapeutic efficacy. Additional data also implicate both PN and NLRP3 production in mediating
migraine-like nociceptive responses. This is exciting as A3AR agonists are already in clinical trials in non-pain
disorders, have a good safety profile, and appear well suited for chronic pain management. Based on these
observations we hypothesize that PN production and activation of its downstream nociceptive signaling cascade
is involved in neuronal and behavioral outcomes in preclinical models of migraine-like headache, and A3AR
agonists inhibit these outcomes, via modulation of this PN signaling cascade. Our goal in Aim 1 will be to validate
A3AR as a novel therapeutic target for migraine-like headache using validated preclinical models of acute and
chronic migraine-like headache and established behavioral and electrophysiological techniques. We will also
measure the temporal expression and localization of A3AR along the migraine pain pathway. In Aim 2, using
pharmacological and genetic approaches, with biochemical analyses, we will test whether the beneficial effects
of A3AR agonists are exerted through inhibition of PN production, and attenuation of post-translational
modifications to neuronal and glial proteins involved in nociceptive glutamatergic neurotransmission and
NLRP3/IL-1β-driven neuroinflammation. Our results are anticipated to provide novel insights into the molecular
neuropharmacology...

## Key facts

- **NIH application ID:** 10363152
- **Project number:** 1R01NS120930-01A1
- **Recipient organization:** UNIVERSITY OF MARYLAND BALTIMORE
- **Principal Investigator:** Simon Akerman
- **Activity code:** R01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2022
- **Award amount:** $498,920
- **Award type:** 1
- **Project period:** 2021-12-01 → 2026-11-30

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10363152

## Citation

> US National Institutes of Health, RePORTER application 10363152, Molecular basis for adenosine A3 receptor agonists in the treatment of migraine (1R01NS120930-01A1). Retrieved via AI Analytics 2026-05-26 from https://api.ai-analytics.org/grant/nih/10363152. Licensed CC0.

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