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Prefrontal and hippocampal theta rhythm show anxiolytic‐like changes during periaqueductal‐elicited “panic” in rats
Anxiety and panic are both elicited by threat and co‐occur clinically. But, at the neural level, anxiety appears to inhibit the generation of panic; and vice versa. Anxiety and panic are thought to engage more anterior (a) and mid‐posterior (m) parts of the periaqueductal gray (PAG), respectively. A...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9540356/ https://www.ncbi.nlm.nih.gov/pubmed/35916172 http://dx.doi.org/10.1002/hipo.23459 |
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author | Silva, Carlos Young, Calvin K. McNaughton, Neil |
author_facet | Silva, Carlos Young, Calvin K. McNaughton, Neil |
author_sort | Silva, Carlos |
collection | PubMed |
description | Anxiety and panic are both elicited by threat and co‐occur clinically. But, at the neural level, anxiety appears to inhibit the generation of panic; and vice versa. Anxiety and panic are thought to engage more anterior (a) and mid‐posterior (m) parts of the periaqueductal gray (PAG), respectively. Anxiety also engages the hippocampus and medial prefrontal cortex. Here, we tested if mPAG but not aPAG stimulation would suppress prefrontal and hippocampal theta rhythm as do anxiolytic drugs. Twelve male rats with implanted electrodes were stimulated alternately (30 s interval) in the left PAG or right reticular formation (reticularis pontis oralis [RPO]—as a positive control) with recording in the left prelimbic cortex and left and right hippocampus. PAG stimulation was set to produce freezing and RPO to produce 7–8 Hz theta rhythm before tests lasting 10 min on each of 5 days. mPAG stimulation decreased, and aPAG increased, theta power at all sites during elicited freezing. mPAG, but not aPAG, stimulation decreased prefrontal theta frequency. Stimulation did not substantially change circuit dynamics (pairwise phase consistency and partial directed coherence). Together with previous reports, our data suggest that panic‐ and anxiety‐control systems are mutually inhibitory, and neural separation of anxiety and panic extends down to the aPAG and mPAG, respectively. Our findings are consistent with recent proposals that fear and anxiety are controlled by parallel neural hierarchies extending from PAG to the prefrontal cortex. |
format | Online Article Text |
id | pubmed-9540356 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95403562022-10-14 Prefrontal and hippocampal theta rhythm show anxiolytic‐like changes during periaqueductal‐elicited “panic” in rats Silva, Carlos Young, Calvin K. McNaughton, Neil Hippocampus Research Articles Anxiety and panic are both elicited by threat and co‐occur clinically. But, at the neural level, anxiety appears to inhibit the generation of panic; and vice versa. Anxiety and panic are thought to engage more anterior (a) and mid‐posterior (m) parts of the periaqueductal gray (PAG), respectively. Anxiety also engages the hippocampus and medial prefrontal cortex. Here, we tested if mPAG but not aPAG stimulation would suppress prefrontal and hippocampal theta rhythm as do anxiolytic drugs. Twelve male rats with implanted electrodes were stimulated alternately (30 s interval) in the left PAG or right reticular formation (reticularis pontis oralis [RPO]—as a positive control) with recording in the left prelimbic cortex and left and right hippocampus. PAG stimulation was set to produce freezing and RPO to produce 7–8 Hz theta rhythm before tests lasting 10 min on each of 5 days. mPAG stimulation decreased, and aPAG increased, theta power at all sites during elicited freezing. mPAG, but not aPAG, stimulation decreased prefrontal theta frequency. Stimulation did not substantially change circuit dynamics (pairwise phase consistency and partial directed coherence). Together with previous reports, our data suggest that panic‐ and anxiety‐control systems are mutually inhibitory, and neural separation of anxiety and panic extends down to the aPAG and mPAG, respectively. Our findings are consistent with recent proposals that fear and anxiety are controlled by parallel neural hierarchies extending from PAG to the prefrontal cortex. John Wiley & Sons, Inc. 2022-08-02 2022-09 /pmc/articles/PMC9540356/ /pubmed/35916172 http://dx.doi.org/10.1002/hipo.23459 Text en © 2022 The Authors. Hippocampus published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Silva, Carlos Young, Calvin K. McNaughton, Neil Prefrontal and hippocampal theta rhythm show anxiolytic‐like changes during periaqueductal‐elicited “panic” in rats |
title | Prefrontal and hippocampal theta rhythm show anxiolytic‐like changes during periaqueductal‐elicited “panic” in rats |
title_full | Prefrontal and hippocampal theta rhythm show anxiolytic‐like changes during periaqueductal‐elicited “panic” in rats |
title_fullStr | Prefrontal and hippocampal theta rhythm show anxiolytic‐like changes during periaqueductal‐elicited “panic” in rats |
title_full_unstemmed | Prefrontal and hippocampal theta rhythm show anxiolytic‐like changes during periaqueductal‐elicited “panic” in rats |
title_short | Prefrontal and hippocampal theta rhythm show anxiolytic‐like changes during periaqueductal‐elicited “panic” in rats |
title_sort | prefrontal and hippocampal theta rhythm show anxiolytic‐like changes during periaqueductal‐elicited “panic” in rats |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9540356/ https://www.ncbi.nlm.nih.gov/pubmed/35916172 http://dx.doi.org/10.1002/hipo.23459 |
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