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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...

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Autores principales: Tavassoli, Zohreh, Javan, Mohammad, Hosseinmardi, Narges, Fathollahi, Yaghoub
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
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.
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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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