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Examination of Diurnal Variation and Sex Differences in Hippocampal Neurophysiology and Spatial Memory
Circadian rhythms are biological processes that cycle across 24 h and regulate many facets of neurophysiology, including learning and memory. Circadian variation in spatial memory task performance is well documented; however, the effect of sex across circadian time (CT) remains unclear. Additionally...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society for Neuroscience
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9668349/ https://www.ncbi.nlm.nih.gov/pubmed/36265903 http://dx.doi.org/10.1523/ENEURO.0124-22.2022 |
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author | Goode, Lacy K. Fusilier, Allison R. Remiszewski, Natalie Reeves, Jacob M. Abiraman, Kavitha Defenderfer, Matthew Paul, Jodi R. McMahon, Lori L. Gamble, Karen L. |
author_facet | Goode, Lacy K. Fusilier, Allison R. Remiszewski, Natalie Reeves, Jacob M. Abiraman, Kavitha Defenderfer, Matthew Paul, Jodi R. McMahon, Lori L. Gamble, Karen L. |
author_sort | Goode, Lacy K. |
collection | PubMed |
description | Circadian rhythms are biological processes that cycle across 24 h and regulate many facets of neurophysiology, including learning and memory. Circadian variation in spatial memory task performance is well documented; however, the effect of sex across circadian time (CT) remains unclear. Additionally, little is known regarding the impact of time-of-day on hippocampal neuronal physiology. Here, we investigated the influence of both sex and time-of-day on hippocampal neurophysiology and memory in mice. Performance on the object location memory (OLM) task depended on both circadian time and sex, with memory enhanced at night in males but during the day in females. Long-term synaptic potentiation (LTP) magnitude at CA3-CA1 synapses was greater at night compared with day in both sexes. Next, we measured spontaneous synaptic excitation and inhibition onto CA1 pyramidal neurons. Frequency and amplitude of inhibition was greater during the day compared with night, regardless of sex. Frequency and amplitude of excitation was larger in females, compared with males, independent of time-of-day, although both time-of-day and sex influenced presynaptic release probability. At night, CA1 pyramidal neurons showed enhanced excitability (action potential firing and/or baseline potential) that was dependent on synaptic excitation and inhibition, regardless of sex. This study emphasizes the importance of sex and time-of-day in hippocampal physiology, especially given that many neurologic disorders impacting the hippocampus are linked to circadian disruption and present differently in men and women. Knowledge about how sex and circadian rhythms affect hippocampal physiology can improve the translational relevancy of therapeutics and inform the appropriate timing of existing treatments. |
format | Online Article Text |
id | pubmed-9668349 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Society for Neuroscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-96683492022-11-17 Examination of Diurnal Variation and Sex Differences in Hippocampal Neurophysiology and Spatial Memory Goode, Lacy K. Fusilier, Allison R. Remiszewski, Natalie Reeves, Jacob M. Abiraman, Kavitha Defenderfer, Matthew Paul, Jodi R. McMahon, Lori L. Gamble, Karen L. eNeuro Research Article: New Research Circadian rhythms are biological processes that cycle across 24 h and regulate many facets of neurophysiology, including learning and memory. Circadian variation in spatial memory task performance is well documented; however, the effect of sex across circadian time (CT) remains unclear. Additionally, little is known regarding the impact of time-of-day on hippocampal neuronal physiology. Here, we investigated the influence of both sex and time-of-day on hippocampal neurophysiology and memory in mice. Performance on the object location memory (OLM) task depended on both circadian time and sex, with memory enhanced at night in males but during the day in females. Long-term synaptic potentiation (LTP) magnitude at CA3-CA1 synapses was greater at night compared with day in both sexes. Next, we measured spontaneous synaptic excitation and inhibition onto CA1 pyramidal neurons. Frequency and amplitude of inhibition was greater during the day compared with night, regardless of sex. Frequency and amplitude of excitation was larger in females, compared with males, independent of time-of-day, although both time-of-day and sex influenced presynaptic release probability. At night, CA1 pyramidal neurons showed enhanced excitability (action potential firing and/or baseline potential) that was dependent on synaptic excitation and inhibition, regardless of sex. This study emphasizes the importance of sex and time-of-day in hippocampal physiology, especially given that many neurologic disorders impacting the hippocampus are linked to circadian disruption and present differently in men and women. Knowledge about how sex and circadian rhythms affect hippocampal physiology can improve the translational relevancy of therapeutics and inform the appropriate timing of existing treatments. Society for Neuroscience 2022-11-08 /pmc/articles/PMC9668349/ /pubmed/36265903 http://dx.doi.org/10.1523/ENEURO.0124-22.2022 Text en Copyright © 2022 Goode et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article: New Research Goode, Lacy K. Fusilier, Allison R. Remiszewski, Natalie Reeves, Jacob M. Abiraman, Kavitha Defenderfer, Matthew Paul, Jodi R. McMahon, Lori L. Gamble, Karen L. Examination of Diurnal Variation and Sex Differences in Hippocampal Neurophysiology and Spatial Memory |
title | Examination of Diurnal Variation and Sex Differences in Hippocampal Neurophysiology and Spatial Memory |
title_full | Examination of Diurnal Variation and Sex Differences in Hippocampal Neurophysiology and Spatial Memory |
title_fullStr | Examination of Diurnal Variation and Sex Differences in Hippocampal Neurophysiology and Spatial Memory |
title_full_unstemmed | Examination of Diurnal Variation and Sex Differences in Hippocampal Neurophysiology and Spatial Memory |
title_short | Examination of Diurnal Variation and Sex Differences in Hippocampal Neurophysiology and Spatial Memory |
title_sort | examination of diurnal variation and sex differences in hippocampal neurophysiology and spatial memory |
topic | Research Article: New Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9668349/ https://www.ncbi.nlm.nih.gov/pubmed/36265903 http://dx.doi.org/10.1523/ENEURO.0124-22.2022 |
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