Imaging Brain Kappa Opioid Receptors in Early Abstinence Opioid Use Disorder

NIH RePORTER · DA · R01 · $810,445 · view on reporter.nih.gov ↗

Abstract

Abstract Imaging Brain Kappa Opioid Receptors in Early Abstinence Opioid Use Disorder The opioid epidemic is one of the worse U.S. public health crises of the past three decades [1]. In response to this epidemic, the National Institute of Health launched a multi-pronged initiative a goal to develop new medications for the treatment of Opioid Use Disorder (OUD) [2]. The kappa Opioid Receptor (NOR) system is a significant driver of continued opioid use, due to its role in negative reinforcement (i.e., the alleviation of negative affect) often referred to as as the “Dark Side of Addiction.” Yet, understanding the role of NOR in OUD, particularly in human subjects, remains in its infancy. To address this gap, we conducted the first preliminary human Positron Emission Tomography (PET) imaging of NOR in people with OUD and saw lower [11C]EKAP binding among abstinent individuals with OUD vs. healthy controls. Our first aim is to use [11C]EKAP PET imaging to compare the magnitude and regional pattern of NOR availability (volume of distribution, VT) of inpatient early abstinent (within 5-10 days of admission) individuals with moderate to severe OUD (N = 40) as compared to matched outpatient healthy controls (HC; N = 30). Our second aim is to establish the clinical and transdiagnostic relevance of NOR by testing whether individual differences in NOR availability: (i) are linked to individual differences in post-inpatient patterns of opioid-use among individuals with OUD; and (ii) are linked to individual differences in experiences of negative affect and anhedonia across all participants (OUD and HC individuals). As tertiary aim: we will establish the clinical and transdiagnostic neural functional correlates of individual differences in NOR by testing whether: (i) individual differences in NOR availability, among OUD subjects, are linked to individual differences in patterns of functional connectivity within a previously identified `opioid abstinence network'[3]; and (ii) if w

Key facts

NIH application ID
11323494
Project number
5R01DA060231-02
Recipient
YALE UNIVERSITY
Principal Investigator
GUSTAVO Adolfo ANGARITA; Ansel Hillmer; DAVID A MATUSKEY; Sarah Yip
Activity code
R01
Funding institute
DA
Fiscal year
2026
Award amount
$810,445
Award type
5
Project period
2025-05-01T00:00:00 → 2030-02-28T00:00:00