Impairment of spatial memory accuracy improved by Cbr1 copy number resumption and GABA


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
25 08 2020
Historique:
received: 21 04 2020
accepted: 10 08 2020
entrez: 27 8 2020
pubmed: 28 8 2020
medline: 12 1 2021
Statut: epublish

Résumé

Down syndrome is a complex genetic disorder caused by the presence of three copies of the chromosome 21 in humans. The most common models, carrying extra-copies of overlapping fragments of mouse chromosome 16 that is syntenic to human chromosome 21, are Ts2Cje, Ts1Cje and Ts1Rhr mice. In electrophysiological analyses using hippocampal slices, we found that the later phase of the depolarization during tetanic stimulation, which was regulated by GABA

Identifiants

pubmed: 32843708
doi: 10.1038/s41598-020-71085-9
pii: 10.1038/s41598-020-71085-9
pmc: PMC7447763
doi:

Substances chimiques

Receptors, GABA-B 0
gamma-Aminobutyric Acid 56-12-2
Alcohol Oxidoreductases EC 1.1.-
carbonyl reductase 1, mouse EC 1.1.-

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

14187

Références

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Auteurs

Fumiko Arima-Yoshida (F)

Division of Neuronal Network, Institute of Medical Science, University of Tokyo, Tokyo, 108-8639, Japan.

Matthieu Raveau (M)

Laboratory for Neurogenetics, RIKEN Center for Brain Science, Wako, Saitama, 351-0198, Japan.

Atsushi Shimohata (A)

Laboratory for Neurogenetics, RIKEN Center for Brain Science, Wako, Saitama, 351-0198, Japan.

Kenji Amano (K)

Laboratory for Neurogenetics, RIKEN Center for Brain Science, Wako, Saitama, 351-0198, Japan.

Akihiro Fukushima (A)

Division of Neuronal Network, Institute of Medical Science, University of Tokyo, Tokyo, 108-8639, Japan.

Masashi Watanave (M)

Division of Neuronal Network, Institute of Medical Science, University of Tokyo, Tokyo, 108-8639, Japan.

Shizuka Kobayashi (S)

Division of Neuronal Network, Institute of Medical Science, University of Tokyo, Tokyo, 108-8639, Japan.

Satoko Hattori (S)

Division of Systems Medical Science, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Aichi, 470-1192, Japan.

Masaya Usui (M)

Research Resources Division, RIKEN Center for Brain Science, Wako, Saitama, 351-0198, Japan.

Haruhiko Sago (H)

Center for Maternal-Fetal, Neonatal and Reproductive Medicine, National Center for Child Health and Development, Tokyo, 157-8535, Japan.

Nobuko Mataga (N)

Research Resources Division, RIKEN Center for Brain Science, Wako, Saitama, 351-0198, Japan.

Tsuyoshi Miyakawa (T)

Division of Systems Medical Science, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Aichi, 470-1192, Japan.

Kazuhiro Yamakawa (K)

Laboratory for Neurogenetics, RIKEN Center for Brain Science, Wako, Saitama, 351-0198, Japan. yamakawa@med.nagoya-cu.ac.jp.
Department of Neurodevelopmental Disorder Genetics, Institute of Brain Sciences, Nagoya City University Graduate School of Medical Sciences, Nagoya, Aichi, 467-8601, Japan. yamakawa@med.nagoya-cu.ac.jp.

Toshiya Manabe (T)

Division of Neuronal Network, Institute of Medical Science, University of Tokyo, Tokyo, 108-8639, Japan. tmanabe-tky@umin.ac.jp.

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