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...
| 出版年: | Scientific Reports |
|---|---|
| 主要な著者: | , , |
| フォーマット: | 論文 |
| 言語: | 英語 |
| 出版事項: |
Nature Portfolio
2025-07-01
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| オンライン・アクセス: | https://doi.org/10.1038/s41598-025-11208-2 |
| _version_ | 1849498888484945920 |
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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. |
| format | Article |
| id | doaj-art-e1c3a5867ac24d6d9d3045e3bd5d5a40 |
| institution | Directory of Open Access Journals |
| issn | 2045-2322 |
| language | English |
| publishDate | 2025-07-01 |
| publisher | Nature Portfolio |
| record_format | Article |
| 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 |
| work_keys_str_mv | AT kailinmmooney absenceofsexdifferencesinserotonergiccontroloforbitofrontalcortexneuronalactivity AT alexanderfhoffman absenceofsexdifferencesinserotonergiccontroloforbitofrontalcortexneuronalactivity AT carlrlupica absenceofsexdifferencesinserotonergiccontroloforbitofrontalcortexneuronalactivity |
