Kappa opioid receptor availability predicts severity of anhedonia in schizophrenia
- PMID: 39217267
- PMCID: PMC11480413
- DOI: 10.1038/s41386-024-01975-3
Kappa opioid receptor availability predicts severity of anhedonia in schizophrenia
Abstract
The kappa opioid receptor (KOR) and its endogenous agonist dynorphin have been implicated in multiple psychiatric conditions including psychotic disorders. We tested the hypotheses that kappa expression is elevated and associated with psychotic symptoms in schizophrenia. We measured kappa expression in unmedicated patients with schizophrenia (7 female, 6 male) and matched controls (7 female, 6 male) with positron emission tomography (PET). We also acquired a measurement of cumulative dopamine activity over the life span in the same subjects using neuromelanin sensitive MRI. We hypothesized that neuromelanin accumulation would be higher in patients than controls and that in patients there would be a positive association between KOR availability and neuromelanin accumulation. Fourteen patients and thirteen controls were enrolled. Whole brain dynamic PET imaging data using the KOR selective tracer [18F]LY245998 were acquired. Distribution volume (VT) was measured with region of interest analysis in 14 brain regions. Neuromelanin accumulation in midbrain dopaminergic nuclei was assessed in the same subjects. Positive and negative symptoms were measured by a clinical psychologist. We did not observe group level differences in KOR expression, neuromelanin accumulation or relationships of these to positive symptoms. Unexpectedly, we did observe strong positive associations between KOR expression and symptoms of anhedonia in the patients (Pearson r > 0.7, uncorrected p < 0.01 in 8 cortical brain regions). We also observed moderate associations between KOR expression and neuromelanin levels in patients. In conclusion, we did not observe a relationship between kappa and symptoms of psychosis but the observed relationship to the negative symptom of anhedonia is in line with recent work testing kappa antagonism as a therapy for anhedonia in depression.
© 2024. The Author(s), under exclusive licence to American College of Neuropsychopharmacology.
Conflict of interest statement
MS is a consultant to Neurocrine Biosciences Inc. GH has an investigator-initiated research agreement with Terran Biosciences and has filed patents for neuromelanin sensitive MRI in central nervous system disorders. AA is on the Scientific Advisory Boards of Neurocrine Biosciences Inc, Boehringer Ingelheim International, and Abbvie, has received honoraria from Sunovion, holds stock in Herophilus, has stock options in Terran Life Sciences and is on the DSMB for Merck. WQ, RG, JJW, GP, TJ-C, JM, BH, and SJM have nothing to report.
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- 5R21MH125454/U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH)
- K23 MH115291/MH/NIMH NIH HHS/United States
- R21 MH125454/MH/NIMH NIH HHS/United States
- 5R21MH125454-02/U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH)
- R21 MH126260/MH/NIMH NIH HHS/United States
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