| Item type |
文献 / Documents(1) |
| 公開日 |
2024-10-01 |
| アクセス権 |
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|
アクセス権 |
open access |
|
アクセス権URI |
http://purl.org/coar/access_right/c_abf2 |
| 資源タイプ |
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|
資源タイプ識別子 |
http://purl.org/coar/resource_type/c_6501 |
|
資源タイプ |
journal article |
| item_1722929371688 |
|
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|
識別子タイプ |
DOI |
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関連識別子 |
https://doi.org/10.1371/journal.pone.0060627 |
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|
言語 |
ja |
|
|
関連名称 |
10.1371/journal.pone.0060627 |
| 出版タイプ |
|
|
出版タイプ |
VoR |
|
出版タイプResource |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
| タイトル |
|
|
タイトル |
Age-Dependent Impairment of Eyeblink Conditioning in Prion Protein-Deficient Mice |
|
言語 |
en |
| タイトル別表記 |
|
|
その他のタイトル |
Eyeblink Conditioning in Prion Protein KO Mice |
|
言語 |
en |
| 著者 |
Kishimoto, Yasushi
Hirono, Moritoshi
Atarashi, Ryuichiro
坂口, 末廣
Yoshioka, Tohru
Katamine, Shigeru
Kirino, Yutaka
|
| 抄録 |
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内容記述タイプ |
Abstract |
|
内容記述 |
Mice lacking the prion protein (PrPC) gene (Prnp), Ngsk Prnp0/0 mice, show late-onset cerebellar Purkinje cell (PC) degeneration because of ectopic overexpression of PrPC-like protein (PrPLP/Dpl). Because PrPC is highly expressed in cerebellar neurons (including PCs and granule cells), it may be involved in cerebellar synaptic function and cerebellar cognitive function. However, no studies have been conducted to investigate the possible involvement of PrPC and/or PrPLP/Dpl in cerebellum-dependent discrete motor learning. Therefore, the present cross-sectional study was designed to examine cerebellum-dependent delay eyeblink conditioning in Ngsk Prnp0/0 mice in adulthood (16, 40, and 60 weeks of age). The aims of the present study were two-fold: (1) to examine the role of PrPC and/or PrPLP/Dpl in cerebellum-dependent motor learning and (2) to confirm the age-related deterioration of eyeblink conditioning in Ngsk Prnp0/0 mice as an animal model of progressive cerebellar degeneration. Ngsk Prnp0/0 mice aged 16 weeks exhibited intact acquisition of conditioned eyeblink responses (CRs), although the CR timing was altered. The same result was observed in another line of PrPc-deficient mice, ZrchI PrnP0/0 mice. However, at 40 weeks of age, CR incidence impairment was observed in Ngsk Prnp0/0 mice. Furthermore, Ngsk Prnp0/0 mice aged 60 weeks showed more significantly impaired CR acquisition than Ngsk Prnp0/0 mice aged 40 weeks, indicating the temporal correlation between cerebellar PC degeneration and motor learning deficits. Our findings indicate the importance of the cerebellar cortex in delay eyeblink conditioning and suggest an important physiological role of prion protein in cerebellar motor learning. |
|
言語 |
en |
| bibliographic_information |
en : PLOS ONE
巻 8,
号 4,
p. e60627,
発行日 2013-04-10
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| 収録物ID |
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|
収録物識別子タイプ |
EISSN |
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収録物識別子 |
19326203 |
| 出版者 |
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出版者 |
PLOS |
|
言語 |
en |
| item_10001_rights_15 |
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言語 |
en |
|
権利情報 |
This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
| item_1723180141928 |
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|
識別子 |
271183 |
|
識別子タイプ |
URI |
| 言語 |
|
|
言語 |
eng |
pone_8_4_e60627.pdf (1012 KB)
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