Optimization of the object recognition assay to test mouse cognition
Background Alzheimer’s disease (AD) has traditionally been recognized as progressive dementia with brain deposits of amyloid (Aβ) and Tau (MAPT) proteins starting 20 and 10 years before the onset of clinical symptoms. Aggregation and deposition of Aβ and Tau proteins have been successfully studied i...
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Published in | Alzheimer's & dementia Vol. 20; no. S1 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken
John Wiley and Sons Inc
01.12.2024
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Abstract | Background
Alzheimer’s disease (AD) has traditionally been recognized as progressive dementia with brain deposits of amyloid (Aβ) and Tau (MAPT) proteins starting 20 and 10 years before the onset of clinical symptoms. Aggregation and deposition of Aβ and Tau proteins have been successfully studied in vitro, cell cultures, and animal models, but clinical deficits have been more difficult to assess. Behavior in mice is a complex phenomenon and subject to variation based on mouse interest, moods, stress‐induced distraction, and other undefined parameters. We have attempted to optimize the novel and displaced object assays to improve behavior studies to evaluate animal models of neurodegeneration.
Method
5xFAD, hTau, and related mice were habituated in the field for 15 minutes twice on day‐1, followed by familiarization with two identical objects twice for 15 minutes on day‐2. The final testing on day‐3 started with novel followed by displaced object analysis. We compared three opaque arenas –rectangular (34 × 24 cm), large square (40 cm), and small square (25 cm) and objects of several heights and types. We also assessed handling mice by cupping to make them more interactive and relaxed for the study.
Result
Mice tend to jump over the arena walls and escape when handled by their tail but are contained when handled by cupping through a cylinder. All the systems were equally able to discriminate between novel and familiar objects. However, we could only distinguish between the familiar and displaced objects in the smaller 25 cm square arena. Also, object interaction time was longer in the smaller field.
Conclusion
It is critical to handle mice by cupping to ensure reduced stress and optimum object interaction. A smaller arena may promote object interaction; taller objects reduce detection artifacts. NIH grants supported the study. |
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AbstractList | Background
Alzheimer’s disease (AD) has traditionally been recognized as progressive dementia with brain deposits of amyloid (Aβ) and Tau (MAPT) proteins starting 20 and 10 years before the onset of clinical symptoms. Aggregation and deposition of Aβ and Tau proteins have been successfully studied in vitro, cell cultures, and animal models, but clinical deficits have been more difficult to assess. Behavior in mice is a complex phenomenon and subject to variation based on mouse interest, moods, stress‐induced distraction, and other undefined parameters. We have attempted to optimize the novel and displaced object assays to improve behavior studies to evaluate animal models of neurodegeneration.
Method
5xFAD, hTau, and related mice were habituated in the field for 15 minutes twice on day‐1, followed by familiarization with two identical objects twice for 15 minutes on day‐2. The final testing on day‐3 started with novel followed by displaced object analysis. We compared three opaque arenas –rectangular (34 × 24 cm), large square (40 cm), and small square (25 cm) and objects of several heights and types. We also assessed handling mice by cupping to make them more interactive and relaxed for the study.
Result
Mice tend to jump over the arena walls and escape when handled by their tail but are contained when handled by cupping through a cylinder. All the systems were equally able to discriminate between novel and familiar objects. However, we could only distinguish between the familiar and displaced objects in the smaller 25 cm square arena. Also, object interaction time was longer in the smaller field.
Conclusion
It is critical to handle mice by cupping to ensure reduced stress and optimum object interaction. A smaller arena may promote object interaction; taller objects reduce detection artifacts. NIH grants supported the study. |
Author | Lahiri, Debomoy K. Crowder, Dallas Shah, Suhua Greig, Nigel H Sambamurti, Kumar Pappolla, Miguel A Fan, Hongkuan Kanthasamy, Anumantha |
AuthorAffiliation | 3 University of Texas Medical Branch, Galveston, TX USA 4 Indiana Alzheimer’s Disease Research Center, Indianapolis, IN USA 1 Medical University of South Carolina, Department of Neurosciences, Charleston, SC USA 2 Medical University of South Carolina, Charleston, SC USA 6 University of Georgia, Athens, GA USA 5 National Institute on Aging, NIH, Baltimore, MD USA |
AuthorAffiliation_xml | – name: 4 Indiana Alzheimer’s Disease Research Center, Indianapolis, IN USA – name: 2 Medical University of South Carolina, Charleston, SC USA – name: 3 University of Texas Medical Branch, Galveston, TX USA – name: 5 National Institute on Aging, NIH, Baltimore, MD USA – name: 6 University of Georgia, Athens, GA USA – name: 1 Medical University of South Carolina, Department of Neurosciences, Charleston, SC USA |
Author_xml | – sequence: 1 givenname: Kumar surname: Sambamurti fullname: Sambamurti, Kumar email: sambak@musc.edu organization: Medical University of South Carolina, Department of Neurosciences, Charleston, SC – sequence: 2 givenname: Dallas surname: Crowder fullname: Crowder, Dallas organization: Medical University of South Carolina, Charleston, SC – sequence: 3 givenname: Miguel A surname: Pappolla fullname: Pappolla, Miguel A organization: University of Texas Medical Branch, Galveston, TX – sequence: 4 givenname: Suhua surname: Shah fullname: Shah, Suhua organization: Medical University of South Carolina, Charleston, SC – sequence: 5 givenname: Hongkuan surname: Fan fullname: Fan, Hongkuan organization: Medical University of South Carolina, Charleston, SC – sequence: 6 givenname: Debomoy K. surname: Lahiri fullname: Lahiri, Debomoy K. organization: Indiana Alzheimer’s Disease Research Center, Indianapolis, IN – sequence: 7 givenname: Nigel H surname: Greig fullname: Greig, Nigel H organization: National Institute on Aging, NIH, Baltimore, MD – sequence: 8 givenname: Anumantha surname: Kanthasamy fullname: Kanthasamy, Anumantha organization: University of Georgia, Athens, GA |
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Copyright | 2024 The Alzheimer's Association. published by Wiley Periodicals LLC on behalf of Alzheimer's Association. |
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Alzheimer’s disease (AD) has traditionally been recognized as progressive dementia with brain deposits of amyloid (Aβ) and Tau (MAPT) proteins... |
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Title | Optimization of the object recognition assay to test mouse cognition |
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