Tooth loss might not alter molecular pathogenesis in an aged transgenic Alzheimer's disease model mouse

Background and objective Previous studies have reported that tooth loss is a risk factor of Alzheimer's disease (AD). However, the association between tooth loss and cognition and the impact of tooth loss on the molecular pathogenesis of AD remain elusive. In this study, we tested the effect of...

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Veröffentlicht in:Gerodontology 2016-09, Vol.33 (3), p.308-314
Hauptverfasser: Oue, Hiroshi, Miyamoto, Yasunari, Koretake, Katsunori, Okada, Shinsuke, Doi, Kazuya, Jung, Cha-Gyun, Michikawa, Makoto, Akagawa, Yasumasa
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container_end_page 314
container_issue 3
container_start_page 308
container_title Gerodontology
container_volume 33
creator Oue, Hiroshi
Miyamoto, Yasunari
Koretake, Katsunori
Okada, Shinsuke
Doi, Kazuya
Jung, Cha-Gyun
Michikawa, Makoto
Akagawa, Yasumasa
description Background and objective Previous studies have reported that tooth loss is a risk factor of Alzheimer's disease (AD). However, the association between tooth loss and cognition and the impact of tooth loss on the molecular pathogenesis of AD remain elusive. In this study, we tested the effect of tooth loss on learning and memory and on the molecular pathogenesis of AD in an aged AD model mice. Materials and methods We divided 14‐month‐old amyloid precursor protein (APP) transgenic mice, an AD model mouse line, into upper molar extracted group (experimental) and molar intact group (control). At 18 months old, we analysed not only the changes of amyloid‐beta (Aβ), pyramidal cells in the brain but also the learning and memory ability with step‐through passive avoidance test. Results The amount of Aβ and the number of pyramidal cells in the hippocampus were not significantly different between the experimental and control group. Similarly, the difference of learning and memory ability could not be distinguished between the groups. Conclusion Neither molecular pathogenesis of AD nor associated learning and memory were aggravated by tooth loss in these mice. The limited results of this study which used the aged mice may help the dental profession to plan and explain treatments to patients with AD, which must be designed while taking into account the severity of the AD symptoms.
doi_str_mv 10.1111/ger.12153
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However, the association between tooth loss and cognition and the impact of tooth loss on the molecular pathogenesis of AD remain elusive. In this study, we tested the effect of tooth loss on learning and memory and on the molecular pathogenesis of AD in an aged AD model mice. Materials and methods We divided 14‐month‐old amyloid precursor protein (APP) transgenic mice, an AD model mouse line, into upper molar extracted group (experimental) and molar intact group (control). At 18 months old, we analysed not only the changes of amyloid‐beta (Aβ), pyramidal cells in the brain but also the learning and memory ability with step‐through passive avoidance test. Results The amount of Aβ and the number of pyramidal cells in the hippocampus were not significantly different between the experimental and control group. Similarly, the difference of learning and memory ability could not be distinguished between the groups. Conclusion Neither molecular pathogenesis of AD nor associated learning and memory were aggravated by tooth loss in these mice. The limited results of this study which used the aged mice may help the dental profession to plan and explain treatments to patients with AD, which must be designed while taking into account the severity of the AD symptoms.</description><identifier>ISSN: 0734-0664</identifier><identifier>EISSN: 1741-2358</identifier><identifier>DOI: 10.1111/ger.12153</identifier><identifier>PMID: 25243637</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Aging ; Alzheimer Disease - pathology ; Alzheimer's disease ; amyloid-β ; Animals ; Dentistry ; Disease Models, Animal ; Hippocampus - cytology ; Learning ; Memory ; Mice ; Mice, Transgenic ; Tg2576 ; tooth loss ; Tooth Loss - pathology</subject><ispartof>Gerodontology, 2016-09, Vol.33 (3), p.308-314</ispartof><rights>2014 John Wiley &amp; Sons A/S and The Gerodontology Association. Published by John Wiley &amp; Sons Ltd</rights><rights>2014 John Wiley &amp; Sons A/S and The Gerodontology Association. 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However, the association between tooth loss and cognition and the impact of tooth loss on the molecular pathogenesis of AD remain elusive. In this study, we tested the effect of tooth loss on learning and memory and on the molecular pathogenesis of AD in an aged AD model mice. Materials and methods We divided 14‐month‐old amyloid precursor protein (APP) transgenic mice, an AD model mouse line, into upper molar extracted group (experimental) and molar intact group (control). At 18 months old, we analysed not only the changes of amyloid‐beta (Aβ), pyramidal cells in the brain but also the learning and memory ability with step‐through passive avoidance test. Results The amount of Aβ and the number of pyramidal cells in the hippocampus were not significantly different between the experimental and control group. Similarly, the difference of learning and memory ability could not be distinguished between the groups. Conclusion Neither molecular pathogenesis of AD nor associated learning and memory were aggravated by tooth loss in these mice. 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However, the association between tooth loss and cognition and the impact of tooth loss on the molecular pathogenesis of AD remain elusive. In this study, we tested the effect of tooth loss on learning and memory and on the molecular pathogenesis of AD in an aged AD model mice. Materials and methods We divided 14‐month‐old amyloid precursor protein (APP) transgenic mice, an AD model mouse line, into upper molar extracted group (experimental) and molar intact group (control). At 18 months old, we analysed not only the changes of amyloid‐beta (Aβ), pyramidal cells in the brain but also the learning and memory ability with step‐through passive avoidance test. Results The amount of Aβ and the number of pyramidal cells in the hippocampus were not significantly different between the experimental and control group. Similarly, the difference of learning and memory ability could not be distinguished between the groups. 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subjects Aging
Alzheimer Disease - pathology
Alzheimer's disease
amyloid-β
Animals
Dentistry
Disease Models, Animal
Hippocampus - cytology
Learning
Memory
Mice
Mice, Transgenic
Tg2576
tooth loss
Tooth Loss - pathology
title Tooth loss might not alter molecular pathogenesis in an aged transgenic Alzheimer's disease model mouse
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