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Active NON-SBIR/STTR RPGS NIH (US)

Dissecting the role of mPFC dynorphin circuits in the modulation of different pain states

$20.69M USD

Funder NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE
Recipient Organization Indiana University Indianapolis
Country United States
Start Date Sep 20, 2024
End Date Aug 31, 2027
Duration 1,075 days
Number of Grantees 1
Roles Principal Investigator
Data Source NIH (US)
Grant ID 10868896
Grant Description

PROJECT SUMMARY The goal of this work is to identify pain-induced adaptations in the prefrontal cortical dynorphin / kappa-opioid receptor system and the role this system plays in pain-induced mal-adaptive behavior and nociception. Chronic pain drives adaptations in prefrontal cortical circuits and is hypothesized to increase bias towards aversive

experiences. Our preliminary data demonstrates that inhibitory and excitatory populations of prefrontal cortical dynorphin neurons are activated and release dynorphin neuropeptide in response to aversive stimuli. However, it is unclear whether prefrontal cortical dynorphin neuron activity and ensuing dynorphin release is impacted by

pain. To address this knowledge gap, we will perform ex-vivo electrophysiological procedures and in-vivo single cell calcium imaging in freely moving mice to determine how pain influences activity of excitatory and inhibitory prefrontal cortical dynorphin neurons and their responsivity to noxious stimuli and aversive stimuli. Moreover, we

will manipulate the activity of prefrontal cortical dynorphin neurons and release of dynorphin neuropeptides or fast transmitters to determine whether enhanced prefrontal cortical dynorphin neuron activity and transmitter release controls nociception and mal-adaptive affective behavior induced by pain. Taken together, this work will

identify how genetically-defined sub-populations of prefrontal cortical neurons and the opioid peptides or fast excitatory and inhibitory transmitters they release influence negative affect induced by pain from the cellular to in-vivo level of analysis. This work is of broad relevance as it elucidates basic principles by which neuropeptide-

expressing neurons in prefrontal cortical circuits control behavioral plasticity and delineate potentially new therapeutic targets for the treatment of mal-adaptive affect and increased responsivity to noxious and aversive stimuli associated with pain states.

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Indiana University Indianapolis

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