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Cholinergic regulation of object recognition memory
Object recognition memory refers to a basic memory mechanism to identify and recall various features of objects. This memory has been investigated by numerous studies in human, primates and rodents to elucidate the neuropsychological underpinnings in mammalian memory, as well as provide the diagnosi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9557046/ https://www.ncbi.nlm.nih.gov/pubmed/36248033 http://dx.doi.org/10.3389/fnbeh.2022.996089 |
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author | Okada, Kana Hashimoto, Kouichi Kobayashi, Kazuto |
author_facet | Okada, Kana Hashimoto, Kouichi Kobayashi, Kazuto |
author_sort | Okada, Kana |
collection | PubMed |
description | Object recognition memory refers to a basic memory mechanism to identify and recall various features of objects. This memory has been investigated by numerous studies in human, primates and rodents to elucidate the neuropsychological underpinnings in mammalian memory, as well as provide the diagnosis of dementia in some neurological diseases, such as Alzheimer’s disease and Parkinson’s disease. Since Alzheimer’s disease at the early stage is reported to be accompanied with cholinergic cell loss and impairment in recognition memory, the central cholinergic system has been studied to investigate the neural mechanism underlying recognition memory. Previous studies have suggested an important role of cholinergic neurons in the acquisition of some variants of object recognition memory in rodents. Cholinergic neurons in the medial septum and ventral diagonal band of Broca that project mainly to the hippocampus and parahippocampal area are related to recognition memory for object location. Cholinergic projections from the nucleus basalis magnocellularis innervating the entire cortex are associated with recognition memory for object identification. Especially, the brain regions that receive cholinergic projections, such as the perirhinal cortex and prefrontal cortex, are involved in recognition memory for object-in-place memory and object recency. In addition, experimental studies using rodent models for Alzheimer’s disease have reported that neurodegeneration within the central cholinergic system causes a deficit in object recognition memory. Elucidating how various types of object recognition memory are regulated by distinct cholinergic cell groups is necessary to clarify the neuronal mechanism for recognition memory and the development of therapeutic treatments for dementia. |
format | Online Article Text |
id | pubmed-9557046 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95570462022-10-14 Cholinergic regulation of object recognition memory Okada, Kana Hashimoto, Kouichi Kobayashi, Kazuto Front Behav Neurosci Neuroscience Object recognition memory refers to a basic memory mechanism to identify and recall various features of objects. This memory has been investigated by numerous studies in human, primates and rodents to elucidate the neuropsychological underpinnings in mammalian memory, as well as provide the diagnosis of dementia in some neurological diseases, such as Alzheimer’s disease and Parkinson’s disease. Since Alzheimer’s disease at the early stage is reported to be accompanied with cholinergic cell loss and impairment in recognition memory, the central cholinergic system has been studied to investigate the neural mechanism underlying recognition memory. Previous studies have suggested an important role of cholinergic neurons in the acquisition of some variants of object recognition memory in rodents. Cholinergic neurons in the medial septum and ventral diagonal band of Broca that project mainly to the hippocampus and parahippocampal area are related to recognition memory for object location. Cholinergic projections from the nucleus basalis magnocellularis innervating the entire cortex are associated with recognition memory for object identification. Especially, the brain regions that receive cholinergic projections, such as the perirhinal cortex and prefrontal cortex, are involved in recognition memory for object-in-place memory and object recency. In addition, experimental studies using rodent models for Alzheimer’s disease have reported that neurodegeneration within the central cholinergic system causes a deficit in object recognition memory. Elucidating how various types of object recognition memory are regulated by distinct cholinergic cell groups is necessary to clarify the neuronal mechanism for recognition memory and the development of therapeutic treatments for dementia. Frontiers Media S.A. 2022-09-29 /pmc/articles/PMC9557046/ /pubmed/36248033 http://dx.doi.org/10.3389/fnbeh.2022.996089 Text en Copyright © 2022 Okada, Hashimoto and Kobayashi. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Okada, Kana Hashimoto, Kouichi Kobayashi, Kazuto Cholinergic regulation of object recognition memory |
title | Cholinergic regulation of object recognition memory |
title_full | Cholinergic regulation of object recognition memory |
title_fullStr | Cholinergic regulation of object recognition memory |
title_full_unstemmed | Cholinergic regulation of object recognition memory |
title_short | Cholinergic regulation of object recognition memory |
title_sort | cholinergic regulation of object recognition memory |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9557046/ https://www.ncbi.nlm.nih.gov/pubmed/36248033 http://dx.doi.org/10.3389/fnbeh.2022.996089 |
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