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Perinatal Penicillin Exposure Affects Cortical Development and Sensory Processing

The prevalent use of antibiotics in pregnant women and neonates raises concerns about long-term risks for children’s health, but their effects on the central nervous system is not well understood. We studied the effects of perinatal penicillin exposure (PPE) on brain structure and function in mice w...

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Autores principales: Perna, James, Lu, Ju, Mullen, Brian, Liu, Taohui, Tjia, Michelle, Weiser, Sydney, Ackman, James, Zuo, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8727458/
https://www.ncbi.nlm.nih.gov/pubmed/35002614
http://dx.doi.org/10.3389/fnmol.2021.704219
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author Perna, James
Lu, Ju
Mullen, Brian
Liu, Taohui
Tjia, Michelle
Weiser, Sydney
Ackman, James
Zuo, Yi
author_facet Perna, James
Lu, Ju
Mullen, Brian
Liu, Taohui
Tjia, Michelle
Weiser, Sydney
Ackman, James
Zuo, Yi
author_sort Perna, James
collection PubMed
description The prevalent use of antibiotics in pregnant women and neonates raises concerns about long-term risks for children’s health, but their effects on the central nervous system is not well understood. We studied the effects of perinatal penicillin exposure (PPE) on brain structure and function in mice with a therapeutically relevant regimen. We used a battery of behavioral tests to evaluate anxiety, working memory, and sensory processing, and immunohistochemistry to quantify changes in parvalbumin-expressing inhibitory interneurons (PV+ INs), perineuronal nets (PNNs), as well as microglia density and morphology. In addition, we performed mesoscale calcium imaging to study neural activity and functional connectivity across cortical regions, and two-photon imaging to monitor dendritic spine and microglial dynamics. We found that adolescent PPE mice have abnormal sensory processing, including impaired texture discrimination and altered prepulse inhibition. Such behavioral changes are associated with increased spontaneous neural activities in various cortical regions, and delayed maturation of PV+ INs in the somatosensory cortex. Furthermore, adolescent PPE mice have elevated elimination of dendritic spines on the apical dendrites of layer 5 pyramidal neurons, as well as increased ramifications and spatial coverage of cortical microglia. Finally, while synaptic defects are transient during adolescence, behavioral abnormalities persist into adulthood. Our study demonstrates that early-life exposure to antibiotics affects cortical development, leaving a lasting effect on brain functions.
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spelling pubmed-87274582022-01-06 Perinatal Penicillin Exposure Affects Cortical Development and Sensory Processing Perna, James Lu, Ju Mullen, Brian Liu, Taohui Tjia, Michelle Weiser, Sydney Ackman, James Zuo, Yi Front Mol Neurosci Neuroscience The prevalent use of antibiotics in pregnant women and neonates raises concerns about long-term risks for children’s health, but their effects on the central nervous system is not well understood. We studied the effects of perinatal penicillin exposure (PPE) on brain structure and function in mice with a therapeutically relevant regimen. We used a battery of behavioral tests to evaluate anxiety, working memory, and sensory processing, and immunohistochemistry to quantify changes in parvalbumin-expressing inhibitory interneurons (PV+ INs), perineuronal nets (PNNs), as well as microglia density and morphology. In addition, we performed mesoscale calcium imaging to study neural activity and functional connectivity across cortical regions, and two-photon imaging to monitor dendritic spine and microglial dynamics. We found that adolescent PPE mice have abnormal sensory processing, including impaired texture discrimination and altered prepulse inhibition. Such behavioral changes are associated with increased spontaneous neural activities in various cortical regions, and delayed maturation of PV+ INs in the somatosensory cortex. Furthermore, adolescent PPE mice have elevated elimination of dendritic spines on the apical dendrites of layer 5 pyramidal neurons, as well as increased ramifications and spatial coverage of cortical microglia. Finally, while synaptic defects are transient during adolescence, behavioral abnormalities persist into adulthood. Our study demonstrates that early-life exposure to antibiotics affects cortical development, leaving a lasting effect on brain functions. Frontiers Media S.A. 2021-12-22 /pmc/articles/PMC8727458/ /pubmed/35002614 http://dx.doi.org/10.3389/fnmol.2021.704219 Text en Copyright © 2021 Perna, Lu, Mullen, Liu, Tjia, Weiser, Ackman and Zuo. 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
Perna, James
Lu, Ju
Mullen, Brian
Liu, Taohui
Tjia, Michelle
Weiser, Sydney
Ackman, James
Zuo, Yi
Perinatal Penicillin Exposure Affects Cortical Development and Sensory Processing
title Perinatal Penicillin Exposure Affects Cortical Development and Sensory Processing
title_full Perinatal Penicillin Exposure Affects Cortical Development and Sensory Processing
title_fullStr Perinatal Penicillin Exposure Affects Cortical Development and Sensory Processing
title_full_unstemmed Perinatal Penicillin Exposure Affects Cortical Development and Sensory Processing
title_short Perinatal Penicillin Exposure Affects Cortical Development and Sensory Processing
title_sort perinatal penicillin exposure affects cortical development and sensory processing
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8727458/
https://www.ncbi.nlm.nih.gov/pubmed/35002614
http://dx.doi.org/10.3389/fnmol.2021.704219
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