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Cortical Cross-Frequency Coupling Is Affected by in utero Exposure to Antidepressant Medication

Up to five percent of human infants are exposed to maternal antidepressant medication by serotonin reuptake inhibitors (SRI) during pregnancy, yet the SRI effects on infants’ early neurodevelopment are not fully understood. Here, we studied how maternal SRI medication affects cortical frequency-spec...

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Autores principales: Tokariev, Anton, Oberlander, Victoria C., Videman, Mari, Vanhatalo, Sampsa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8927083/
https://www.ncbi.nlm.nih.gov/pubmed/35310093
http://dx.doi.org/10.3389/fnins.2022.803708
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author Tokariev, Anton
Oberlander, Victoria C.
Videman, Mari
Vanhatalo, Sampsa
author_facet Tokariev, Anton
Oberlander, Victoria C.
Videman, Mari
Vanhatalo, Sampsa
author_sort Tokariev, Anton
collection PubMed
description Up to five percent of human infants are exposed to maternal antidepressant medication by serotonin reuptake inhibitors (SRI) during pregnancy, yet the SRI effects on infants’ early neurodevelopment are not fully understood. Here, we studied how maternal SRI medication affects cortical frequency-specific and cross-frequency interactions estimated, respectively, by phase-phase correlations (PPC) and phase-amplitude coupling (PAC) in electroencephalographic (EEG) recordings. We examined the cortical activity in infants after fetal exposure to SRIs relative to a control group of infants without medical history of any kind. Our findings show that the sleep-related dynamics of PPC networks are selectively affected by in utero SRI exposure, however, those alterations do not correlate to later neurocognitive development as tested by neuropsychological evaluation at two years of age. In turn, phase-amplitude coupling was found to be suppressed in SRI infants across multiple distributed cortical regions and these effects were linked to their neurocognitive outcomes. Our results are compatible with the overall notion that in utero drug exposures may cause subtle, yet measurable changes in the brain structure and function. Our present findings are based on the measures of local and inter-areal neuronal interactions in the cortex which can be readily used across species, as well as between different scales of inspection: from the whole animals to in vitro preparations. Therefore, this work opens a framework to explore the cellular and molecular mechanisms underlying neurodevelopmental SRI effects at all translational levels.
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spelling pubmed-89270832022-03-18 Cortical Cross-Frequency Coupling Is Affected by in utero Exposure to Antidepressant Medication Tokariev, Anton Oberlander, Victoria C. Videman, Mari Vanhatalo, Sampsa Front Neurosci Neuroscience Up to five percent of human infants are exposed to maternal antidepressant medication by serotonin reuptake inhibitors (SRI) during pregnancy, yet the SRI effects on infants’ early neurodevelopment are not fully understood. Here, we studied how maternal SRI medication affects cortical frequency-specific and cross-frequency interactions estimated, respectively, by phase-phase correlations (PPC) and phase-amplitude coupling (PAC) in electroencephalographic (EEG) recordings. We examined the cortical activity in infants after fetal exposure to SRIs relative to a control group of infants without medical history of any kind. Our findings show that the sleep-related dynamics of PPC networks are selectively affected by in utero SRI exposure, however, those alterations do not correlate to later neurocognitive development as tested by neuropsychological evaluation at two years of age. In turn, phase-amplitude coupling was found to be suppressed in SRI infants across multiple distributed cortical regions and these effects were linked to their neurocognitive outcomes. Our results are compatible with the overall notion that in utero drug exposures may cause subtle, yet measurable changes in the brain structure and function. Our present findings are based on the measures of local and inter-areal neuronal interactions in the cortex which can be readily used across species, as well as between different scales of inspection: from the whole animals to in vitro preparations. Therefore, this work opens a framework to explore the cellular and molecular mechanisms underlying neurodevelopmental SRI effects at all translational levels. Frontiers Media S.A. 2022-03-03 /pmc/articles/PMC8927083/ /pubmed/35310093 http://dx.doi.org/10.3389/fnins.2022.803708 Text en Copyright © 2022 Tokariev, Oberlander, Videman and Vanhatalo. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Tokariev, Anton
Oberlander, Victoria C.
Videman, Mari
Vanhatalo, Sampsa
Cortical Cross-Frequency Coupling Is Affected by in utero Exposure to Antidepressant Medication
title Cortical Cross-Frequency Coupling Is Affected by in utero Exposure to Antidepressant Medication
title_full Cortical Cross-Frequency Coupling Is Affected by in utero Exposure to Antidepressant Medication
title_fullStr Cortical Cross-Frequency Coupling Is Affected by in utero Exposure to Antidepressant Medication
title_full_unstemmed Cortical Cross-Frequency Coupling Is Affected by in utero Exposure to Antidepressant Medication
title_short Cortical Cross-Frequency Coupling Is Affected by in utero Exposure to Antidepressant Medication
title_sort cortical cross-frequency coupling is affected by in utero exposure to antidepressant medication
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8927083/
https://www.ncbi.nlm.nih.gov/pubmed/35310093
http://dx.doi.org/10.3389/fnins.2022.803708
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