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  1. 原著論文

P301S mutant human tau transgenic mice manifest early symptoms of human tauopathies with dementia and altered sensorimotor gating

https://repo.qst.go.jp/records/47233
https://repo.qst.go.jp/records/47233
e047a335-1e60-4f71-bb44-9ed1c1e6edfa
Item type 学術雑誌論文 / Journal Article(1)
公開日 2015-08-06
タイトル
タイトル P301S mutant human tau transgenic mice manifest early symptoms of human tauopathies with dementia and altered sensorimotor gating
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Takeuchi, Hiroki

× Takeuchi, Hiroki

WEKO 472326

Takeuchi, Hiroki

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Iba, Michiyo

× Iba, Michiyo

WEKO 472327

Iba, Michiyo

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Inoue, Haruhisa

× Inoue, Haruhisa

WEKO 472328

Inoue, Haruhisa

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Higuchi, Makoto

× Higuchi, Makoto

WEKO 472329

Higuchi, Makoto

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Takao, Keizo

× Takao, Keizo

WEKO 472330

Takao, Keizo

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Tsukita, Kayoko

× Tsukita, Kayoko

WEKO 472331

Tsukita, Kayoko

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Karatsu, Yoshiko

× Karatsu, Yoshiko

WEKO 472332

Karatsu, Yoshiko

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Iwamoto, Yumiko

× Iwamoto, Yumiko

WEKO 472333

Iwamoto, Yumiko

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Miyakawa, Tsuyoshi

× Miyakawa, Tsuyoshi

WEKO 472334

Miyakawa, Tsuyoshi

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Suhara, Tetsuya

× Suhara, Tetsuya

WEKO 472335

Suhara, Tetsuya

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Q., Trojanowski John

× Q., Trojanowski John

WEKO 472336

Q., Trojanowski John

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M., -Y. Lee Virginia

× M., -Y. Lee Virginia

WEKO 472337

M., -Y. Lee Virginia

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Takahashi, Ryosuke

× Takahashi, Ryosuke

WEKO 472338

Takahashi, Ryosuke

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竹内 啓喜

× 竹内 啓喜

WEKO 472339

en 竹内 啓喜

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樋口 真人

× 樋口 真人

WEKO 472340

en 樋口 真人

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須原 哲也

× 須原 哲也

WEKO 472341

en 須原 哲也

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抄録
内容記述タイプ Abstract
内容記述 Tauopathies are neurodegenerative disorders characterized by the accumulation of abnormal tau protein leading to cognitive and/or motor dysfunction. To understand the relationship between tau pathology and behavioral impairments, we comprehensively assessed behavioral abnormalities in a mouse tauopathy model expressing the human P301S mutant tau protein in the early stage of disease to detect its initial neurological manifestations. Behavioral abnormalities, shown by open field test, elevated plus-maze test, hot plate test, Y-maze test, Barnes maze test, Morris water maze test, and/or contextual fear conditioning test, recapitulated the neurological deficits of human tauopathies with dementia. Furthermore, we discovered that prepulse inhibition (PPI), a marker of sensorimotor gating, was enhanced in these animals concomitantly with initial neuropathological changes in associated brain regions. This finding provides evidence that our tauopathy mouse model displays neurofunctional abnormalities in prodromal stages of disease, since enhancement of PPI is characteristic of amnestic mild cognitive impairment, a transitional stage between normal aging and dementia such as Alzheimer's disease (AD), in contrast with attenuated PPI in AD patients. Therefore, assessment of sensorimotor gating could be used to detect the earliest manifestations of tauopathies exemplified by prodromal AD, in which abnormal tau protein may play critical roles in the onset of neuronal dysfunctions.
書誌情報 PLoS ONE (Online only:URL:http://www.plosone.org)

巻 6, 号 6, p. e21050-e21050, 発行日 2011-06
ISSN
収録物識別子タイプ ISSN
収録物識別子 1932-6203
PubMed番号
識別子タイプ PMID
関連識別子 1698260
DOI
識別子タイプ DOI
関連識別子 10.1371/journal.pone.0021050
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