The AMPA receptor positive allosteric modulator S 47445 rescues in vivo CA3-CA1 long-term potentiation and structural synaptic changes in old mice

dc.contributor.author
Giralt Torroella, Albert
dc.contributor.author
Gómez Climent, María Ángeles
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Alcalá Vida, Rafael
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Bretin, Sylvie
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Bertrand, Daniel
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Delgado García, José M.
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Pérez Navarro, Esther
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Alberch i Vié, Jordi, 1959-
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Gruart i Massó, Agnès
dc.date.issued
2020-05-15T18:53:21Z
dc.date.issued
2020-05-15T18:53:21Z
dc.date.issued
2017-09-01
dc.date.issued
2020-05-15T18:53:21Z
dc.identifier
0028-3908
dc.identifier
https://hdl.handle.net/2445/160592
dc.identifier
679685
dc.identifier
28603025
dc.description.abstract
Positive allosteric modulators of cc-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors (AMPARs) are small molecules that decrease deactivation of AMPARs via an allosteric site. These molecules keep the receptor in an active state. Interestingly, this type of modulator has been proposed for treating cognitive decline in ageing, dementias, and Alzheimer's disease (AD). S 47445 (8-cyclopropyl-3[2-(3-fluorophenyflethy1]-7,8-dihydro-3H-[1,3]oxazino[6,5-g][1,2,3]benzotriazine-4,9-dione) is a novel AMPAR positive allosteric modulator (AMPA-PAM). Here, the mechanisms by which S 47445 could improve synaptic strength and connectivity were studied and compared between young and old mice. A single oral administration of S 47445 at 10 mg/kg significantly increased long-term potentiation (LTP) in CA3-CA1 hippocampal synapses in alert young mice in comparison to control mice. Moreover, chronic treatment with S 47445 at 10 mg/kg in old alert animals significantly counteracted the deficit of LTP due to age. Accordingly, chronic treatment with S 47445 at 10 mg/kg seems to preserve synaptic cytoarchitecture in old mice as compared with young control mice. It was shown that the significant decreases in number and size of pre-synaptic buttons stained for VGlutl, and post-synaptic dendritic spines stained for spinophilin, observed in old mice were significantly prevented after chronic treatment with 10 mg/kg of S 47445. Altogether, by its different effects on LTP, VGlutl-positive particles, and spinophilin, S 47445 is able to modulate both the structure and function of hippocampal excitatory synapses known to be involved in learning and memory processes. These results open a new window for the treatment of specific age-dependent cognitive decline and dementias such as AD. (C) 2017 The Authors. Published by Elsevier Ltd.
dc.format
15 p.
dc.format
application/pdf
dc.language
eng
dc.publisher
Elsevier Ltd
dc.relation
Reproducció del document publicat a: https://doi.org/10.1016/j.neuropharm.2017.06.009
dc.relation
Neuropharmacology, 2017, vol. 123, p. 395-409
dc.relation
https://doi.org/10.1016/j.neuropharm.2017.06.009
dc.rights
cc-by-nc-nd (c) Elsevier Ltd, 2017
dc.rights
http://creativecommons.org/licenses/by-nc-nd/3.0/es
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Biomedicina)
dc.subject
Models animals en la investigació
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Malaltia d'Alzheimer
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Malalties neurodegeneratives
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Receptors de neurotransmissors
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Animal models in research
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Alzheimer's disease
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Neurodegenerative Diseases
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Neurotransmitter receptors
dc.title
The AMPA receptor positive allosteric modulator S 47445 rescues in vivo CA3-CA1 long-term potentiation and structural synaptic changes in old mice
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/acceptedVersion


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