Absence of sex differences in serotonergic control of orbitofrontal cortex neuronal activity

Abstract The orbitofrontal cortex (OFC) is a brain region involved in cognitive processing, especially in tasks that require flexibility in decision-making. Serotonin (5-HT) plays a critical role in mediating OFC-dependent behavior, primarily through its actions at both 5-HT1 and 5-HT2 receptors. Th...

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出版年:Scientific Reports
主要な著者: Kailin M. Mooney, Alexander F. Hoffman, Carl R. Lupica
フォーマット: 論文
言語:英語
出版事項: Nature Portfolio 2025-07-01
オンライン・アクセス:https://doi.org/10.1038/s41598-025-11208-2
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author Kailin M. Mooney
Alexander F. Hoffman
Carl R. Lupica
author_facet Kailin M. Mooney
Alexander F. Hoffman
Carl R. Lupica
author_sort Kailin M. Mooney
collection DOAJ
container_title Scientific Reports
description Abstract The orbitofrontal cortex (OFC) is a brain region involved in cognitive processing, especially in tasks that require flexibility in decision-making. Serotonin (5-HT) plays a critical role in mediating OFC-dependent behavior, primarily through its actions at both 5-HT1 and 5-HT2 receptors. Through these receptors, 5-HT acts both pre- and postsynaptically at pyramidal (PyN) neurons and parvalbumin-containing interneurons (OFCPV) to regulate their activity. In a previous study, we reported that the non-selective 5-HT2 antagonist ketanserin inhibited 5-HT-induced membrane currents in OFCPV neurons from female and not male rats, suggesting the possibility that this results from sex-dependent differential 5-HT2A and 5-HT2C receptor expression. Here, we test this hypothesis using subtype-selective antagonists, and we find that 5-HT-mediated depolarization of OFCPV neurons occurs via activation of 5-HT2A, and not 5-HT2C receptors. Additionally, 5-HT2A receptor antagonism was equally effective in OFCPV neurons from males and females, as was the 5-HT2 agonist 2,5-Dimethoxy-4-iodoamphetamine (DOI). These pharmacological data suggest that the sex-dependent effects of ketanserin do not result from differential expression of 5-HT2 receptor subtypes in OFCPV neurons. In addition, 5-HT effects on OFC PyNs are similar in males and females. In light of recent reports of sex-dependent differences in prefrontal cortical function, our results are presented to inform and clarify actions of 5-HT on OFC circuitry.
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spelling doaj-art-e1c3a5867ac24d6d9d3045e3bd5d5a402025-08-20T03:04:29ZengNature PortfolioScientific Reports2045-23222025-07-0115111110.1038/s41598-025-11208-2Absence of sex differences in serotonergic control of orbitofrontal cortex neuronal activityKailin M. Mooney0Alexander F. Hoffman1Carl R. Lupica2U.S. Department of Health and Human Services, National Institutes of Health, National Institute on Drug Abuse Intramural Research Program, Cellular and Neurocomputational Systems Branch, Electrophysiology Research SectionU.S. Department of Health and Human Services, National Institutes of Health, National Institute on Drug Abuse Intramural Research Program, Cellular and Neurocomputational Systems Branch, Electrophysiology Research SectionU.S. Department of Health and Human Services, National Institutes of Health, National Institute on Drug Abuse Intramural Research Program, Cellular and Neurocomputational Systems Branch, Electrophysiology Research SectionAbstract The orbitofrontal cortex (OFC) is a brain region involved in cognitive processing, especially in tasks that require flexibility in decision-making. Serotonin (5-HT) plays a critical role in mediating OFC-dependent behavior, primarily through its actions at both 5-HT1 and 5-HT2 receptors. Through these receptors, 5-HT acts both pre- and postsynaptically at pyramidal (PyN) neurons and parvalbumin-containing interneurons (OFCPV) to regulate their activity. In a previous study, we reported that the non-selective 5-HT2 antagonist ketanserin inhibited 5-HT-induced membrane currents in OFCPV neurons from female and not male rats, suggesting the possibility that this results from sex-dependent differential 5-HT2A and 5-HT2C receptor expression. Here, we test this hypothesis using subtype-selective antagonists, and we find that 5-HT-mediated depolarization of OFCPV neurons occurs via activation of 5-HT2A, and not 5-HT2C receptors. Additionally, 5-HT2A receptor antagonism was equally effective in OFCPV neurons from males and females, as was the 5-HT2 agonist 2,5-Dimethoxy-4-iodoamphetamine (DOI). These pharmacological data suggest that the sex-dependent effects of ketanserin do not result from differential expression of 5-HT2 receptor subtypes in OFCPV neurons. In addition, 5-HT effects on OFC PyNs are similar in males and females. In light of recent reports of sex-dependent differences in prefrontal cortical function, our results are presented to inform and clarify actions of 5-HT on OFC circuitry.https://doi.org/10.1038/s41598-025-11208-2
spellingShingle Kailin M. Mooney
Alexander F. Hoffman
Carl R. Lupica
Absence of sex differences in serotonergic control of orbitofrontal cortex neuronal activity
title Absence of sex differences in serotonergic control of orbitofrontal cortex neuronal activity
title_full Absence of sex differences in serotonergic control of orbitofrontal cortex neuronal activity
title_fullStr Absence of sex differences in serotonergic control of orbitofrontal cortex neuronal activity
title_full_unstemmed Absence of sex differences in serotonergic control of orbitofrontal cortex neuronal activity
title_short Absence of sex differences in serotonergic control of orbitofrontal cortex neuronal activity
title_sort absence of sex differences in serotonergic control of orbitofrontal cortex neuronal activity
url https://doi.org/10.1038/s41598-025-11208-2
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