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Tooth Loss Induces Memory Impairment and Glial Activation in Young Wild-Type Mice

BACKGROUND: Tooth loss is closely associated with Alzheimer’s disease (AD). Previously, we reported that tooth loss induced memory impairment in amyloid precursor protein knock-in mice by decreasing neuronal activity and synaptic protein levels and increasing glial activation, neuroinflammation, and...

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Autores principales: Taslima, Ferdous, Abdelhamid, Mona, Zhou, Chunyu, Chen, Yuxin, Jung, Cha-Gyun, Michikawa, Makoto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9696677/
https://www.ncbi.nlm.nih.gov/pubmed/36506484
http://dx.doi.org/10.3233/ADR-220053
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author Taslima, Ferdous
Abdelhamid, Mona
Zhou, Chunyu
Chen, Yuxin
Jung, Cha-Gyun
Michikawa, Makoto
author_facet Taslima, Ferdous
Abdelhamid, Mona
Zhou, Chunyu
Chen, Yuxin
Jung, Cha-Gyun
Michikawa, Makoto
author_sort Taslima, Ferdous
collection PubMed
description BACKGROUND: Tooth loss is closely associated with Alzheimer’s disease (AD). Previously, we reported that tooth loss induced memory impairment in amyloid precursor protein knock-in mice by decreasing neuronal activity and synaptic protein levels and increasing glial activation, neuroinflammation, and pyramidal neuronal cell loss without altering amyloid-β levels in the hippocampus. However, the effects of tooth loss in young wild-type mice have not been explored yet. OBJECTIVE: We investigated the effects of tooth loss on memory impairment, neuronal activity, synaptic protein levels, glial activation, and pyramidal neuronal cell loss in young wild-type mice. METHODS: Two-month-old wild-type mice were randomly divided into control and tooth loss groups. In the tooth loss group, maxillary molar teeth on both sides were extracted, whereas no teeth were extracted in the control group. Two months after tooth extraction, we performed a novel object recognition test to evaluate memory function. Glial activation, neuronal activity, synaptic protein levels, and the number of pyramidal neurons were evaluated using immunofluorescence staining, immunohistochemistry, and western blotting. RESULTS: The tooth loss group exhibited memory impairment and decreased neuronal activity and the levels of synaptic proteins in both the hippocampus and cortex. Moreover, tooth loss increased the activation of phosphorylated c-Jun N-terminal kinase (JNK), heat shock protein 90 (HSP90), and glial activation and reduced the number of pyramidal neurons in the hippocampus. CONCLUSION: Tooth loss in the young wild-type mice will attenuate neuronal activity, decrease synaptic protein levels, and induce pyramidal neuronal loss, and eventually lead to memory impairment.
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spelling pubmed-96966772022-12-08 Tooth Loss Induces Memory Impairment and Glial Activation in Young Wild-Type Mice Taslima, Ferdous Abdelhamid, Mona Zhou, Chunyu Chen, Yuxin Jung, Cha-Gyun Michikawa, Makoto J Alzheimers Dis Rep Research Report BACKGROUND: Tooth loss is closely associated with Alzheimer’s disease (AD). Previously, we reported that tooth loss induced memory impairment in amyloid precursor protein knock-in mice by decreasing neuronal activity and synaptic protein levels and increasing glial activation, neuroinflammation, and pyramidal neuronal cell loss without altering amyloid-β levels in the hippocampus. However, the effects of tooth loss in young wild-type mice have not been explored yet. OBJECTIVE: We investigated the effects of tooth loss on memory impairment, neuronal activity, synaptic protein levels, glial activation, and pyramidal neuronal cell loss in young wild-type mice. METHODS: Two-month-old wild-type mice were randomly divided into control and tooth loss groups. In the tooth loss group, maxillary molar teeth on both sides were extracted, whereas no teeth were extracted in the control group. Two months after tooth extraction, we performed a novel object recognition test to evaluate memory function. Glial activation, neuronal activity, synaptic protein levels, and the number of pyramidal neurons were evaluated using immunofluorescence staining, immunohistochemistry, and western blotting. RESULTS: The tooth loss group exhibited memory impairment and decreased neuronal activity and the levels of synaptic proteins in both the hippocampus and cortex. Moreover, tooth loss increased the activation of phosphorylated c-Jun N-terminal kinase (JNK), heat shock protein 90 (HSP90), and glial activation and reduced the number of pyramidal neurons in the hippocampus. CONCLUSION: Tooth loss in the young wild-type mice will attenuate neuronal activity, decrease synaptic protein levels, and induce pyramidal neuronal loss, and eventually lead to memory impairment. IOS Press 2022-11-03 /pmc/articles/PMC9696677/ /pubmed/36506484 http://dx.doi.org/10.3233/ADR-220053 Text en © 2022 – The authors. Published by IOS Press https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Report
Taslima, Ferdous
Abdelhamid, Mona
Zhou, Chunyu
Chen, Yuxin
Jung, Cha-Gyun
Michikawa, Makoto
Tooth Loss Induces Memory Impairment and Glial Activation in Young Wild-Type Mice
title Tooth Loss Induces Memory Impairment and Glial Activation in Young Wild-Type Mice
title_full Tooth Loss Induces Memory Impairment and Glial Activation in Young Wild-Type Mice
title_fullStr Tooth Loss Induces Memory Impairment and Glial Activation in Young Wild-Type Mice
title_full_unstemmed Tooth Loss Induces Memory Impairment and Glial Activation in Young Wild-Type Mice
title_short Tooth Loss Induces Memory Impairment and Glial Activation in Young Wild-Type Mice
title_sort tooth loss induces memory impairment and glial activation in young wild-type mice
topic Research Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9696677/
https://www.ncbi.nlm.nih.gov/pubmed/36506484
http://dx.doi.org/10.3233/ADR-220053
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