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Contribution of the μ‐opioid receptor system to affective disorders in temporal lobe epilepsy: A bidirectional relationship?

OBJECTIVE: Affective disorders are frequent comorbidities of temporal lobe epilepsy (TLE). The endogenous opioid system has been implicated in both epilepsy and affective disorders, and may play a significant role in their bidirectional relationship. In this cross‐sectional study, we investigated th...

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Autores principales: Sone, Daichi, Galovic, Marian, Myers, Jim, Leonhardt, Georg, Rabiner, Ilan, Duncan, John S., Koepp, Matthias J., Foong, Jacqueline
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107876/
https://www.ncbi.nlm.nih.gov/pubmed/36377838
http://dx.doi.org/10.1111/epi.17463
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author Sone, Daichi
Galovic, Marian
Myers, Jim
Leonhardt, Georg
Rabiner, Ilan
Duncan, John S.
Koepp, Matthias J.
Foong, Jacqueline
author_facet Sone, Daichi
Galovic, Marian
Myers, Jim
Leonhardt, Georg
Rabiner, Ilan
Duncan, John S.
Koepp, Matthias J.
Foong, Jacqueline
author_sort Sone, Daichi
collection PubMed
description OBJECTIVE: Affective disorders are frequent comorbidities of temporal lobe epilepsy (TLE). The endogenous opioid system has been implicated in both epilepsy and affective disorders, and may play a significant role in their bidirectional relationship. In this cross‐sectional study, we investigated the association between μ‐opioid receptor binding and affective disorders in patients with TLE. METHODS: Nine patients with TLE and depression/anxiety underwent (11)C‐carfentanil positron emission tomography (CFN PET) and neuropsychiatric assessment, including the Hospital Anxiety and Depression Scale and the Positive and Negative Affect Schedule. The normalized CFN PET scans were compared with those of 26 age‐matched healthy controls. Correlation analyses with affective symptoms were performed by region of interest‐based analysis focusing on the limbic circuit and orbitofrontal cortex. RESULTS: We observed widely reduced CFN binding potential (BP) in bilateral frontal lobes and striata in patients with TLE compared to healthy controls. In the TLE group, more severe anxiety and negative affect were associated with decreased CFN BP in the posterior cingulate gyrus. SIGNIFICANCE: In patients with TLE, interictally reduced binding in the opioid system was associated with higher levels of anxiety and negative affect. We speculate that seizure‐related agonist‐driven desensitization and downregulation of opioid receptors could be a potential underlying pathomechanism.
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spelling pubmed-101078762023-04-18 Contribution of the μ‐opioid receptor system to affective disorders in temporal lobe epilepsy: A bidirectional relationship? Sone, Daichi Galovic, Marian Myers, Jim Leonhardt, Georg Rabiner, Ilan Duncan, John S. Koepp, Matthias J. Foong, Jacqueline Epilepsia Research Articles OBJECTIVE: Affective disorders are frequent comorbidities of temporal lobe epilepsy (TLE). The endogenous opioid system has been implicated in both epilepsy and affective disorders, and may play a significant role in their bidirectional relationship. In this cross‐sectional study, we investigated the association between μ‐opioid receptor binding and affective disorders in patients with TLE. METHODS: Nine patients with TLE and depression/anxiety underwent (11)C‐carfentanil positron emission tomography (CFN PET) and neuropsychiatric assessment, including the Hospital Anxiety and Depression Scale and the Positive and Negative Affect Schedule. The normalized CFN PET scans were compared with those of 26 age‐matched healthy controls. Correlation analyses with affective symptoms were performed by region of interest‐based analysis focusing on the limbic circuit and orbitofrontal cortex. RESULTS: We observed widely reduced CFN binding potential (BP) in bilateral frontal lobes and striata in patients with TLE compared to healthy controls. In the TLE group, more severe anxiety and negative affect were associated with decreased CFN BP in the posterior cingulate gyrus. SIGNIFICANCE: In patients with TLE, interictally reduced binding in the opioid system was associated with higher levels of anxiety and negative affect. We speculate that seizure‐related agonist‐driven desensitization and downregulation of opioid receptors could be a potential underlying pathomechanism. John Wiley and Sons Inc. 2022-12-28 2023-02 /pmc/articles/PMC10107876/ /pubmed/36377838 http://dx.doi.org/10.1111/epi.17463 Text en © 2022 The Authors. Epilepsia published by Wiley Periodicals LLC on behalf of International League Against Epilepsy. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Sone, Daichi
Galovic, Marian
Myers, Jim
Leonhardt, Georg
Rabiner, Ilan
Duncan, John S.
Koepp, Matthias J.
Foong, Jacqueline
Contribution of the μ‐opioid receptor system to affective disorders in temporal lobe epilepsy: A bidirectional relationship?
title Contribution of the μ‐opioid receptor system to affective disorders in temporal lobe epilepsy: A bidirectional relationship?
title_full Contribution of the μ‐opioid receptor system to affective disorders in temporal lobe epilepsy: A bidirectional relationship?
title_fullStr Contribution of the μ‐opioid receptor system to affective disorders in temporal lobe epilepsy: A bidirectional relationship?
title_full_unstemmed Contribution of the μ‐opioid receptor system to affective disorders in temporal lobe epilepsy: A bidirectional relationship?
title_short Contribution of the μ‐opioid receptor system to affective disorders in temporal lobe epilepsy: A bidirectional relationship?
title_sort contribution of the μ‐opioid receptor system to affective disorders in temporal lobe epilepsy: a bidirectional relationship?
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107876/
https://www.ncbi.nlm.nih.gov/pubmed/36377838
http://dx.doi.org/10.1111/epi.17463
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