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Electrical impulses evoked activity patterns in ventral tegmental area and locus coeruleus modulate endogenous and learning-dependent disparity of cell proliferation along the mouse dentate gyrus
This study aimed to examine the effects of the ventral tegmental area (VTA) and the locus coeruleus (LC) patterned electrical stimulation on hippocampal-dependent learning and hippocampal neurogenesis in adult mouse. For this, mice were given unilateral electrical stimulation of VTA or LC using phas...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10300460/ https://www.ncbi.nlm.nih.gov/pubmed/37388501 http://dx.doi.org/10.1016/j.ibneur.2023.03.002 |
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author | Tavassoli, Zohreh Javan, Mohammad Hosseinmardi, Narges Fathollahi, Yaghoub |
author_facet | Tavassoli, Zohreh Javan, Mohammad Hosseinmardi, Narges Fathollahi, Yaghoub |
author_sort | Tavassoli, Zohreh |
collection | PubMed |
description | This study aimed to examine the effects of the ventral tegmental area (VTA) and the locus coeruleus (LC) patterned electrical stimulation on hippocampal-dependent learning and hippocampal neurogenesis in adult mouse. For this, mice were given unilateral electrical stimulation of VTA or LC using phasic or tonic stimulation protocols. Behavior acquisition rates were evaluated using the Barnes maze (BM) and a passive avoidance (PA) task. Cell proliferation was measured in the dorsal (dDG), intermediate (iDG) and ventral (vDG) dentate gyrus (DG) using Ki67 immunohistochemistry. We showed that the levels of cell proliferation were significantly different in three highlighted parts of the DG. The behavioral testing paradigms themselves were sufficient to alter cell proliferation indices along the dentate gyrus. The phasic LC modulation treatment enhanced behavioral acquisition of the BM and cell proliferation in the dDG, while tonic VTA stimulation improved PA acquisition and increased cell proliferation in the iDG. It is concluded that electrical impulses-evoked phasic or tonic activity patterns in the LC and VTA could modulate endogenous and learning dependent disparity of cell proliferation along the adult mouse DG. |
format | Online Article Text |
id | pubmed-10300460 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-103004602023-06-29 Electrical impulses evoked activity patterns in ventral tegmental area and locus coeruleus modulate endogenous and learning-dependent disparity of cell proliferation along the mouse dentate gyrus Tavassoli, Zohreh Javan, Mohammad Hosseinmardi, Narges Fathollahi, Yaghoub IBRO Neurosci Rep Research Paper This study aimed to examine the effects of the ventral tegmental area (VTA) and the locus coeruleus (LC) patterned electrical stimulation on hippocampal-dependent learning and hippocampal neurogenesis in adult mouse. For this, mice were given unilateral electrical stimulation of VTA or LC using phasic or tonic stimulation protocols. Behavior acquisition rates were evaluated using the Barnes maze (BM) and a passive avoidance (PA) task. Cell proliferation was measured in the dorsal (dDG), intermediate (iDG) and ventral (vDG) dentate gyrus (DG) using Ki67 immunohistochemistry. We showed that the levels of cell proliferation were significantly different in three highlighted parts of the DG. The behavioral testing paradigms themselves were sufficient to alter cell proliferation indices along the dentate gyrus. The phasic LC modulation treatment enhanced behavioral acquisition of the BM and cell proliferation in the dDG, while tonic VTA stimulation improved PA acquisition and increased cell proliferation in the iDG. It is concluded that electrical impulses-evoked phasic or tonic activity patterns in the LC and VTA could modulate endogenous and learning dependent disparity of cell proliferation along the adult mouse DG. Elsevier 2023-03-08 /pmc/articles/PMC10300460/ /pubmed/37388501 http://dx.doi.org/10.1016/j.ibneur.2023.03.002 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Paper Tavassoli, Zohreh Javan, Mohammad Hosseinmardi, Narges Fathollahi, Yaghoub Electrical impulses evoked activity patterns in ventral tegmental area and locus coeruleus modulate endogenous and learning-dependent disparity of cell proliferation along the mouse dentate gyrus |
title | Electrical impulses evoked activity patterns in ventral tegmental area and locus coeruleus modulate endogenous and learning-dependent disparity of cell proliferation along the mouse dentate gyrus |
title_full | Electrical impulses evoked activity patterns in ventral tegmental area and locus coeruleus modulate endogenous and learning-dependent disparity of cell proliferation along the mouse dentate gyrus |
title_fullStr | Electrical impulses evoked activity patterns in ventral tegmental area and locus coeruleus modulate endogenous and learning-dependent disparity of cell proliferation along the mouse dentate gyrus |
title_full_unstemmed | Electrical impulses evoked activity patterns in ventral tegmental area and locus coeruleus modulate endogenous and learning-dependent disparity of cell proliferation along the mouse dentate gyrus |
title_short | Electrical impulses evoked activity patterns in ventral tegmental area and locus coeruleus modulate endogenous and learning-dependent disparity of cell proliferation along the mouse dentate gyrus |
title_sort | electrical impulses evoked activity patterns in ventral tegmental area and locus coeruleus modulate endogenous and learning-dependent disparity of cell proliferation along the mouse dentate gyrus |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10300460/ https://www.ncbi.nlm.nih.gov/pubmed/37388501 http://dx.doi.org/10.1016/j.ibneur.2023.03.002 |
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