Cargando…
Cholinergic stimulation modulates the functional composition of CA3 cell types in the hippocampus
The functional heterogeneity of hippocampal CA3 pyramidal neurons has emerged as a key aspect of circuit function. Here, we explored the effects of long-term cholinergic activity on the functional heterogeneity of CA3 pyramidal neurons in organotypic slices obtained from male rat brains. Application...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10324996/ https://www.ncbi.nlm.nih.gov/pubmed/37277177 http://dx.doi.org/10.1523/JNEUROSCI.0966-22.2023 |
_version_ | 1785069217353039872 |
---|---|
author | Puhl, Christopher Jon Wefelmeyer, Winnie Burrone, Juan |
author_facet | Puhl, Christopher Jon Wefelmeyer, Winnie Burrone, Juan |
author_sort | Puhl, Christopher Jon |
collection | PubMed |
description | The functional heterogeneity of hippocampal CA3 pyramidal neurons has emerged as a key aspect of circuit function. Here, we explored the effects of long-term cholinergic activity on the functional heterogeneity of CA3 pyramidal neurons in organotypic slices obtained from male rat brains. Application of agonists to either acetylcholine receptors (AChRs) generally, or muscarinic AChRs (mAChRs) specifically, induced robust increases in network activity in the low-gamma range. Prolonged AChR stimulation for 48 hrs uncovered a population of hyperadapting CA3 pyramidal neurons that typically fired a single, early action potential in response to current injection. Although these neurons were present in control networks, their proportions were dramatically increased following long-term cholinergic activity. Characterised by the presence of a strong M-current, the hyperadaptation phenotype was abolished by acute application of either M-channel antagonists or the re-application of AChR agonists. We conclude that long-term mAChR activation modulates the intrinsic excitability of a subset of CA3 pyramidal cells, uncovering a highly plastic cohort of neurons that are sensitive to chronic ACh modulation. Our findings provide evidence for the activity-dependent plasticity of functional heterogeneity in the hippocampus. |
format | Online Article Text |
id | pubmed-10324996 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
record_format | MEDLINE/PubMed |
spelling | pubmed-103249962023-07-10 Cholinergic stimulation modulates the functional composition of CA3 cell types in the hippocampus Puhl, Christopher Jon Wefelmeyer, Winnie Burrone, Juan J Neurosci Article The functional heterogeneity of hippocampal CA3 pyramidal neurons has emerged as a key aspect of circuit function. Here, we explored the effects of long-term cholinergic activity on the functional heterogeneity of CA3 pyramidal neurons in organotypic slices obtained from male rat brains. Application of agonists to either acetylcholine receptors (AChRs) generally, or muscarinic AChRs (mAChRs) specifically, induced robust increases in network activity in the low-gamma range. Prolonged AChR stimulation for 48 hrs uncovered a population of hyperadapting CA3 pyramidal neurons that typically fired a single, early action potential in response to current injection. Although these neurons were present in control networks, their proportions were dramatically increased following long-term cholinergic activity. Characterised by the presence of a strong M-current, the hyperadaptation phenotype was abolished by acute application of either M-channel antagonists or the re-application of AChR agonists. We conclude that long-term mAChR activation modulates the intrinsic excitability of a subset of CA3 pyramidal cells, uncovering a highly plastic cohort of neurons that are sensitive to chronic ACh modulation. Our findings provide evidence for the activity-dependent plasticity of functional heterogeneity in the hippocampus. 2023-07-05 2023-06-05 /pmc/articles/PMC10324996/ /pubmed/37277177 http://dx.doi.org/10.1523/JNEUROSCI.0966-22.2023 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a CC BY 4.0 (https://creativecommons.org/licenses/by/4.0/) International license. |
spellingShingle | Article Puhl, Christopher Jon Wefelmeyer, Winnie Burrone, Juan Cholinergic stimulation modulates the functional composition of CA3 cell types in the hippocampus |
title | Cholinergic stimulation modulates the functional composition of CA3 cell types in the hippocampus |
title_full | Cholinergic stimulation modulates the functional composition of CA3 cell types in the hippocampus |
title_fullStr | Cholinergic stimulation modulates the functional composition of CA3 cell types in the hippocampus |
title_full_unstemmed | Cholinergic stimulation modulates the functional composition of CA3 cell types in the hippocampus |
title_short | Cholinergic stimulation modulates the functional composition of CA3 cell types in the hippocampus |
title_sort | cholinergic stimulation modulates the functional composition of ca3 cell types in the hippocampus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10324996/ https://www.ncbi.nlm.nih.gov/pubmed/37277177 http://dx.doi.org/10.1523/JNEUROSCI.0966-22.2023 |
work_keys_str_mv | AT puhlchristopherjon cholinergicstimulationmodulatesthefunctionalcompositionofca3celltypesinthehippocampus AT wefelmeyerwinnie cholinergicstimulationmodulatesthefunctionalcompositionofca3celltypesinthehippocampus AT burronejuan cholinergicstimulationmodulatesthefunctionalcompositionofca3celltypesinthehippocampus |