The DOI matches its Crossref record; 42 of the 42 references it cites were found in a registry or an index.
Onset of hippocampus-dependent memory impairments in 5XFAD transgenic mouse model of Alzheimer’s disease
Abstract
The 5XFAD mice are an early‐onset transgenic model of Alzheimer's disease (AD) in which amyloid plaques are first observed between two and four months of age in the cortical layer five and in the subiculum of the hippocampal formation. Although cognitive alterations have been described in these mice, there are no studies that focused on the onset of hippocampus‐dependent memory deficits, which are a hallmark of the prodromal stage of AD. To identify when the first learning and memory impairments appear, 5XFAD mice of two, four, and six months of age were compared with their respective wild‐type littermates using the olfactory tubing maze, which is a very sensitive hippocampal‐dependent task. Deficits in learning and memory started at four months with a substantial increase at six months of age while no olfactory impairments were observed. The volumetric study using magnetic resonance imaging of the whole brain and specific areas (olfactory bulb, striatum, and hippocampus) did not reveal neuro‐anatomical difference. Slight memory deficits appeared at 4 months of age in correlation with an increased astrogliosis and amyloid plaque formation. This early impairment in learning and memory related to the hippocampal dysfunction is particularly suited to assess preclinical therapeutic strategies aiming to delay or suppress the onset of AD. © 2014 Wiley Periodicals, Inc.
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“Interestingly, behavioral and memory deficits do not typically begin to show significant differences in 5xFAD animals until at least 5-7 months of age (Girard et al., 2014; Ohno, 2009).”
From LC3-Associated Endocytosis Facilitates β-Amyloid Clearance and Mitigates Neurodegeneration in Murine Alzheimer’s Disease (2019) · cites this paper as Girard et al., 2014
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Cites
The mouse brain in stereotaxic coordinates
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“…take at least 6–12 months to form amyloid plaques (Eriksen and Janus, 2007), the 5XFAD transgenic mice used in this study are one of the most early onset and aggressive amyloid mouse models with a development starting at two months of age (Oakley et al., 2006; Ohno et al., 2006, 2007; Ohno, 2009).”
BackgroundMethodResultInfluentialImpaired synaptic plasticity and learning in aged amyloid precursor protein transgenic mice
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“This finding is in agreement with a recent report demonstrating with unbiased stereology that 5XFAD mice develop a significant selective neuron loss in layer five of the cortex from 12 months of age but the overall neuron number in the entire frontal cortex and hippocampus was unaffected (Jawhar et al., 2012).”
ResultMemory and Brain Systems: 1969–2009
Squire, L. R. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.3575-09.2009 · Cited by 550
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Research works printed but not linked: 1
- O'leary TP, 2011, Poster presented at the 41st annual meeting of the Society for Neuroscience
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Heckmann, B. L., Teubner, B. J. W., Tummers, B., Boada-Romero, E., Harris, L., Yang, M., Guy, C. S., Zakharenko, S. S., & Green, D. R. (2019) · Cell · doi:10.1016/j.cell.2019.05.056 · Cited by 503
“Interestingly, behavioral and memory deficits do not typically begin to show significant differences in 5xFAD animals until at least 5-7 months of age (Girard et al., 2014; Ohno, 2009).”
Landel, V., Baranger, K., Virard, I., Loriod, B., Khrestchatisky, M., Rivera, S., Benech, P., & Féron, F. (2014) · Molecular Neurodegeneration · doi:10.1186/1750-1326-9-33 · Cited by 176
Self-citationBaranger, K., Marchalant, Y., Bonnet, A. E., Crouzin, N., Carrete, A., Paumier, J.-M., Py, N. A., Bernard, A., Bauer, C., Charrat, E., et al. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-015-1992-1 · Cited by 133
Self-citationSex Differences in Behavior and Molecular Pathology in the 5XFAD Model
Sil, A., Erfani, A., Lamb, N., Copland, R., Riedel, G., & Platt, B. (2022) · Journal of Alzheimer's Disease · doi:10.3233/jad-210523 · Cited by 109
Rivera, S., García-González, L., Khrestchatisky, M., & Baranger, K. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-019-03178-2 · Cited by 111
Self-citation
Metadata
- Authors
- Girard, S. D., Jacquet, M., Baranger, K., Migliorati, M., Escoffier, G., Bernard, A., Khrestchatisky, M., Féron, F., Rivera, S., Roman, F. S., & Marchetti, E.
- Affiliations
- Centre National de la Recherche Scientifique (FR)
- Aix Marseille Université, CNRS, NICN, UMR7259 Marseille France
- Corresponding author
- Roman, François S.
- ORCID
- Venue
- Hippocampus
- Publisher
- Wiley
- Published
- 2014-03-14
- Volume
- 24
- Issue
- 7
- Pages
- 762-772
- ISSN
- 1050-9631 (ISSN-L)
- 1098-1063
- OpenAlex
- W1532925865
- Cited by
- 119
- References
- 42
- Citations by year
- 2026: 13 · 2025: 7 · 2024: 13 · 2023: 13 · 2022: 22 · 2021: 14 · 2020: 5 · 2019: 9 · 2018: 8 · 2017: 5 · 2016: 3 · 2015: 3 · 2014: 4
- FWCI
- 3.32
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Hippocampus (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Keywords
- 5xFAD mice, Alzheimer's disease, hippocampal-dependent memory, learning and memory impairment, prodromal Alzheimer's disease, amyloid plaques, astrocyte activation, olfactory bulb, hippocampal dysfunction
- MeSH terms
- Alzheimer Disease, Animals, Astrocytes, Corpus Striatum, Gliosis, Hippocampus, Learning Disabilities, Magnetic Resonance Imaging, Male, Memory Disorders, Mice, Transgenic, Olfactory Bulb, Organ Size, Smell, Amyloid beta-Protein Precursor, Point Mutation, Age of Onset, Maze Learning, Mice, Presenilin-1, Plaque, Amyloid
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