Olfactory and visuospatial learning and memory performance in two strains of Alzheimer's disease model mice--a longitudinal study
Using a longitudinal study design, two strains of Alzheimer's disease (AD) model mice, one expressing β-amyloid plaques and one expressing Tau protein-associated neurofibrillary tangles were assessed for olfactory and visuospatial learning and memory and their performance compared to that of ag...
Gespeichert in:
Veröffentlicht in: | PloS one 2011-05, Vol.6 (5), p.e19567-e19567 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | e19567 |
---|---|
container_issue | 5 |
container_start_page | e19567 |
container_title | PloS one |
container_volume | 6 |
creator | Phillips, Matthew Boman, Erik Osterman, Hanna Willhite, David Laska, Matthias |
description | Using a longitudinal study design, two strains of Alzheimer's disease (AD) model mice, one expressing β-amyloid plaques and one expressing Tau protein-associated neurofibrillary tangles were assessed for olfactory and visuospatial learning and memory and their performance compared to that of age-matched controls. No significant difference between AD and control mice was found in the initial set of olfactory tasks performed at 6 months of age whereas both strains of AD mice performed significantly poorer than the controls in visuospatial learning at this age. Subsequent tests performed on the same individual animals at 7, 8, 9, 11, 13, 15, and 18 months of age also failed to find systematic differences in olfactory performance between AD and control mice. In contrast, the AD mice performed consistently poorer than the controls in visuospatial re-learning tests performed at these ages. With most olfactory tasks, both AD and control mice displayed a marked decrease in performance between testing at 15 and 18 months of age. These results show that the two strains of AD model mice do not display an olfactory impairment in a time course consistent with human AD, but are impaired in visuospatial capabilities. The marked age-related changes observed with the olfactory tasks in both AD and control mice suggest that the observed lack of an AD-related olfactory impairment is not due to an insensitivity of the tests employed. Rather, they suggest that the olfactory system of the two AD mouse model strains may be surprisingly robust against AD-typical neuropathologies. |
doi_str_mv | 10.1371/journal.pone.0019567 |
format | Article |
fullrecord | <record><control><sourceid>gale_plos_</sourceid><recordid>TN_cdi_plos_journals_1295065371</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A476892101</galeid><doaj_id>oai_doaj_org_article_fcead2eb729443c487150f939df9a718</doaj_id><sourcerecordid>A476892101</sourcerecordid><originalsourceid>FETCH-LOGICAL-c691t-babcad735a5ef98225e58087f2799881938bdac51b51a24c4b7babc5e7806ec03</originalsourceid><addsrcrecordid>eNqNk0tv1DAUhSMEoqXwDxBEQqJiMYMdx7G9QaoqHpUqVeK1tW6cmxlXjj3YSaHs-Oc47bTqoC6QF7Hs7xz7HucWxXNKlpQJ-vY8TNGDW26CxyUhVPFGPCj2qWLVoqkIe3hnvlc8SemcEM5k0zwu9irKBaON2C_-nLkezBjiZQm-Ky9smkLawGjBlQ4heutXVzsDDjO0wdiHOIA3WFpfjj9DmcYI1qcy9OWR-71GO2A8TGVnE0LCcggdunKwBhcLKF3wKztOnc1Xz8qpu3xaPOrBJXy2_R4U3z68_3r8aXF69vHk-Oh0YRpFx0ULrYFOMA4ceyWriiOXRIq-EkpJmUuVbQeG05ZTqGpTt2KWcBSSNGgIOyheXvtuXEh6m17StFKcNDwnmomTa6ILcK430Q4QL3UAq68WQlxpiKM1DnVvELoKW1GpumamloJy0iumul6BoDJ7vdueNrUDdgZ9TsntmO7ueLvWq3ChGZGyESobHG4NYvgxYRr1YJNB58BjmJLOEKs4I3Nhr_4h7y9uS60g39_6PuRjzeypj2rRSFVRMlPLe6g8OswvmP-03ub1HcGbHUFmRvw1rmBKSZ98-fz_7Nn3Xfb1HXaN4MZ1Cm4abfBpF6yvQRNDShH724wp0XOj3KSh50bR20bJshd33-dWdNMZ7C8fXg_5</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1295065371</pqid></control><display><type>article</type><title>Olfactory and visuospatial learning and memory performance in two strains of Alzheimer's disease model mice--a longitudinal study</title><source>MEDLINE</source><source>DOAJ Directory of Open Access Journals</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><source>Free Full-Text Journals in Chemistry</source><source>Public Library of Science (PLoS)</source><creator>Phillips, Matthew ; Boman, Erik ; Osterman, Hanna ; Willhite, David ; Laska, Matthias</creator><creatorcontrib>Phillips, Matthew ; Boman, Erik ; Osterman, Hanna ; Willhite, David ; Laska, Matthias</creatorcontrib><description>Using a longitudinal study design, two strains of Alzheimer's disease (AD) model mice, one expressing β-amyloid plaques and one expressing Tau protein-associated neurofibrillary tangles were assessed for olfactory and visuospatial learning and memory and their performance compared to that of age-matched controls. No significant difference between AD and control mice was found in the initial set of olfactory tasks performed at 6 months of age whereas both strains of AD mice performed significantly poorer than the controls in visuospatial learning at this age. Subsequent tests performed on the same individual animals at 7, 8, 9, 11, 13, 15, and 18 months of age also failed to find systematic differences in olfactory performance between AD and control mice. In contrast, the AD mice performed consistently poorer than the controls in visuospatial re-learning tests performed at these ages. With most olfactory tasks, both AD and control mice displayed a marked decrease in performance between testing at 15 and 18 months of age. These results show that the two strains of AD model mice do not display an olfactory impairment in a time course consistent with human AD, but are impaired in visuospatial capabilities. The marked age-related changes observed with the olfactory tasks in both AD and control mice suggest that the observed lack of an AD-related olfactory impairment is not due to an insensitivity of the tests employed. Rather, they suggest that the olfactory system of the two AD mouse model strains may be surprisingly robust against AD-typical neuropathologies.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0019567</identifier><identifier>PMID: 21573167</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Advertising executives ; Age ; Aging ; Aging - physiology ; Alzheimer Disease - pathology ; Alzheimer Disease - physiopathology ; Alzheimer's disease ; Alzheimers disease ; Animal cognition ; Animals ; Biology ; Cognitive ability ; Comparative analysis ; Correlation analysis ; Disease Models, Animal ; Epidermal growth factor ; Habituation, Psychophysiologic ; Impairment ; Laboratory animals ; Learning ; Longitudinal Studies ; Medical research ; Memory ; Memory - physiology ; Mice ; Mice, Inbred Strains ; Mutation ; Neurobiology ; Neurodegenerative diseases ; Neurofibrillary tangles ; Neurogenesis ; Neuropathology ; Neurosciences ; Odorants ; Older people ; Olfactory discrimination learning ; Olfactory Pathways - physiology ; Olfactory system ; Physical Stimulation ; Physics ; Proteins ; Rodents ; Senile plaques ; Smell ; Spatial memory ; Task Performance and Analysis ; Tau protein ; Transgenic animals ; Visual Pathways - physiology ; Zoology ; β-Amyloid</subject><ispartof>PloS one, 2011-05, Vol.6 (5), p.e19567-e19567</ispartof><rights>COPYRIGHT 2011 Public Library of Science</rights><rights>2011 Phillips et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Phillips et al. 2011</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c691t-babcad735a5ef98225e58087f2799881938bdac51b51a24c4b7babc5e7806ec03</citedby><cites>FETCH-LOGICAL-c691t-babcad735a5ef98225e58087f2799881938bdac51b51a24c4b7babc5e7806ec03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3088679/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3088679/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23845,27901,27902,53766,53768,79342,79343</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21573167$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Phillips, Matthew</creatorcontrib><creatorcontrib>Boman, Erik</creatorcontrib><creatorcontrib>Osterman, Hanna</creatorcontrib><creatorcontrib>Willhite, David</creatorcontrib><creatorcontrib>Laska, Matthias</creatorcontrib><title>Olfactory and visuospatial learning and memory performance in two strains of Alzheimer's disease model mice--a longitudinal study</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Using a longitudinal study design, two strains of Alzheimer's disease (AD) model mice, one expressing β-amyloid plaques and one expressing Tau protein-associated neurofibrillary tangles were assessed for olfactory and visuospatial learning and memory and their performance compared to that of age-matched controls. No significant difference between AD and control mice was found in the initial set of olfactory tasks performed at 6 months of age whereas both strains of AD mice performed significantly poorer than the controls in visuospatial learning at this age. Subsequent tests performed on the same individual animals at 7, 8, 9, 11, 13, 15, and 18 months of age also failed to find systematic differences in olfactory performance between AD and control mice. In contrast, the AD mice performed consistently poorer than the controls in visuospatial re-learning tests performed at these ages. With most olfactory tasks, both AD and control mice displayed a marked decrease in performance between testing at 15 and 18 months of age. These results show that the two strains of AD model mice do not display an olfactory impairment in a time course consistent with human AD, but are impaired in visuospatial capabilities. The marked age-related changes observed with the olfactory tasks in both AD and control mice suggest that the observed lack of an AD-related olfactory impairment is not due to an insensitivity of the tests employed. Rather, they suggest that the olfactory system of the two AD mouse model strains may be surprisingly robust against AD-typical neuropathologies.</description><subject>Advertising executives</subject><subject>Age</subject><subject>Aging</subject><subject>Aging - physiology</subject><subject>Alzheimer Disease - pathology</subject><subject>Alzheimer Disease - physiopathology</subject><subject>Alzheimer's disease</subject><subject>Alzheimers disease</subject><subject>Animal cognition</subject><subject>Animals</subject><subject>Biology</subject><subject>Cognitive ability</subject><subject>Comparative analysis</subject><subject>Correlation analysis</subject><subject>Disease Models, Animal</subject><subject>Epidermal growth factor</subject><subject>Habituation, Psychophysiologic</subject><subject>Impairment</subject><subject>Laboratory animals</subject><subject>Learning</subject><subject>Longitudinal Studies</subject><subject>Medical research</subject><subject>Memory</subject><subject>Memory - physiology</subject><subject>Mice</subject><subject>Mice, Inbred Strains</subject><subject>Mutation</subject><subject>Neurobiology</subject><subject>Neurodegenerative diseases</subject><subject>Neurofibrillary tangles</subject><subject>Neurogenesis</subject><subject>Neuropathology</subject><subject>Neurosciences</subject><subject>Odorants</subject><subject>Older people</subject><subject>Olfactory discrimination learning</subject><subject>Olfactory Pathways - physiology</subject><subject>Olfactory system</subject><subject>Physical Stimulation</subject><subject>Physics</subject><subject>Proteins</subject><subject>Rodents</subject><subject>Senile plaques</subject><subject>Smell</subject><subject>Spatial memory</subject><subject>Task Performance and Analysis</subject><subject>Tau protein</subject><subject>Transgenic animals</subject><subject>Visual Pathways - physiology</subject><subject>Zoology</subject><subject>β-Amyloid</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><sourceid>DOA</sourceid><recordid>eNqNk0tv1DAUhSMEoqXwDxBEQqJiMYMdx7G9QaoqHpUqVeK1tW6cmxlXjj3YSaHs-Oc47bTqoC6QF7Hs7xz7HucWxXNKlpQJ-vY8TNGDW26CxyUhVPFGPCj2qWLVoqkIe3hnvlc8SemcEM5k0zwu9irKBaON2C_-nLkezBjiZQm-Ky9smkLawGjBlQ4heutXVzsDDjO0wdiHOIA3WFpfjj9DmcYI1qcy9OWR-71GO2A8TGVnE0LCcggdunKwBhcLKF3wKztOnc1Xz8qpu3xaPOrBJXy2_R4U3z68_3r8aXF69vHk-Oh0YRpFx0ULrYFOMA4ceyWriiOXRIq-EkpJmUuVbQeG05ZTqGpTt2KWcBSSNGgIOyheXvtuXEh6m17StFKcNDwnmomTa6ILcK430Q4QL3UAq68WQlxpiKM1DnVvELoKW1GpumamloJy0iumul6BoDJ7vdueNrUDdgZ9TsntmO7ueLvWq3ChGZGyESobHG4NYvgxYRr1YJNB58BjmJLOEKs4I3Nhr_4h7y9uS60g39_6PuRjzeypj2rRSFVRMlPLe6g8OswvmP-03ub1HcGbHUFmRvw1rmBKSZ98-fz_7Nn3Xfb1HXaN4MZ1Cm4abfBpF6yvQRNDShH724wp0XOj3KSh50bR20bJshd33-dWdNMZ7C8fXg_5</recordid><startdate>20110505</startdate><enddate>20110505</enddate><creator>Phillips, Matthew</creator><creator>Boman, Erik</creator><creator>Osterman, Hanna</creator><creator>Willhite, David</creator><creator>Laska, Matthias</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20110505</creationdate><title>Olfactory and visuospatial learning and memory performance in two strains of Alzheimer's disease model mice--a longitudinal study</title><author>Phillips, Matthew ; Boman, Erik ; Osterman, Hanna ; Willhite, David ; Laska, Matthias</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c691t-babcad735a5ef98225e58087f2799881938bdac51b51a24c4b7babc5e7806ec03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Advertising executives</topic><topic>Age</topic><topic>Aging</topic><topic>Aging - physiology</topic><topic>Alzheimer Disease - pathology</topic><topic>Alzheimer Disease - physiopathology</topic><topic>Alzheimer's disease</topic><topic>Alzheimers disease</topic><topic>Animal cognition</topic><topic>Animals</topic><topic>Biology</topic><topic>Cognitive ability</topic><topic>Comparative analysis</topic><topic>Correlation analysis</topic><topic>Disease Models, Animal</topic><topic>Epidermal growth factor</topic><topic>Habituation, Psychophysiologic</topic><topic>Impairment</topic><topic>Laboratory animals</topic><topic>Learning</topic><topic>Longitudinal Studies</topic><topic>Medical research</topic><topic>Memory</topic><topic>Memory - physiology</topic><topic>Mice</topic><topic>Mice, Inbred Strains</topic><topic>Mutation</topic><topic>Neurobiology</topic><topic>Neurodegenerative diseases</topic><topic>Neurofibrillary tangles</topic><topic>Neurogenesis</topic><topic>Neuropathology</topic><topic>Neurosciences</topic><topic>Odorants</topic><topic>Older people</topic><topic>Olfactory discrimination learning</topic><topic>Olfactory Pathways - physiology</topic><topic>Olfactory system</topic><topic>Physical Stimulation</topic><topic>Physics</topic><topic>Proteins</topic><topic>Rodents</topic><topic>Senile plaques</topic><topic>Smell</topic><topic>Spatial memory</topic><topic>Task Performance and Analysis</topic><topic>Tau protein</topic><topic>Transgenic animals</topic><topic>Visual Pathways - physiology</topic><topic>Zoology</topic><topic>β-Amyloid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Phillips, Matthew</creatorcontrib><creatorcontrib>Boman, Erik</creatorcontrib><creatorcontrib>Osterman, Hanna</creatorcontrib><creatorcontrib>Willhite, David</creatorcontrib><creatorcontrib>Laska, Matthias</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials Science Collection</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Phillips, Matthew</au><au>Boman, Erik</au><au>Osterman, Hanna</au><au>Willhite, David</au><au>Laska, Matthias</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Olfactory and visuospatial learning and memory performance in two strains of Alzheimer's disease model mice--a longitudinal study</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2011-05-05</date><risdate>2011</risdate><volume>6</volume><issue>5</issue><spage>e19567</spage><epage>e19567</epage><pages>e19567-e19567</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Using a longitudinal study design, two strains of Alzheimer's disease (AD) model mice, one expressing β-amyloid plaques and one expressing Tau protein-associated neurofibrillary tangles were assessed for olfactory and visuospatial learning and memory and their performance compared to that of age-matched controls. No significant difference between AD and control mice was found in the initial set of olfactory tasks performed at 6 months of age whereas both strains of AD mice performed significantly poorer than the controls in visuospatial learning at this age. Subsequent tests performed on the same individual animals at 7, 8, 9, 11, 13, 15, and 18 months of age also failed to find systematic differences in olfactory performance between AD and control mice. In contrast, the AD mice performed consistently poorer than the controls in visuospatial re-learning tests performed at these ages. With most olfactory tasks, both AD and control mice displayed a marked decrease in performance between testing at 15 and 18 months of age. These results show that the two strains of AD model mice do not display an olfactory impairment in a time course consistent with human AD, but are impaired in visuospatial capabilities. The marked age-related changes observed with the olfactory tasks in both AD and control mice suggest that the observed lack of an AD-related olfactory impairment is not due to an insensitivity of the tests employed. Rather, they suggest that the olfactory system of the two AD mouse model strains may be surprisingly robust against AD-typical neuropathologies.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>21573167</pmid><doi>10.1371/journal.pone.0019567</doi><tpages>e19567</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2011-05, Vol.6 (5), p.e19567-e19567 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_1295065371 |
source | MEDLINE; DOAJ Directory of Open Access Journals; EZB-FREE-00999 freely available EZB journals; PubMed Central; Free Full-Text Journals in Chemistry; Public Library of Science (PLoS) |
subjects | Advertising executives Age Aging Aging - physiology Alzheimer Disease - pathology Alzheimer Disease - physiopathology Alzheimer's disease Alzheimers disease Animal cognition Animals Biology Cognitive ability Comparative analysis Correlation analysis Disease Models, Animal Epidermal growth factor Habituation, Psychophysiologic Impairment Laboratory animals Learning Longitudinal Studies Medical research Memory Memory - physiology Mice Mice, Inbred Strains Mutation Neurobiology Neurodegenerative diseases Neurofibrillary tangles Neurogenesis Neuropathology Neurosciences Odorants Older people Olfactory discrimination learning Olfactory Pathways - physiology Olfactory system Physical Stimulation Physics Proteins Rodents Senile plaques Smell Spatial memory Task Performance and Analysis Tau protein Transgenic animals Visual Pathways - physiology Zoology β-Amyloid |
title | Olfactory and visuospatial learning and memory performance in two strains of Alzheimer's disease model mice--a longitudinal study |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-08T11%3A38%3A03IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Olfactory%20and%20visuospatial%20learning%20and%20memory%20performance%20in%20two%20strains%20of%20Alzheimer's%20disease%20model%20mice--a%20longitudinal%20study&rft.jtitle=PloS%20one&rft.au=Phillips,%20Matthew&rft.date=2011-05-05&rft.volume=6&rft.issue=5&rft.spage=e19567&rft.epage=e19567&rft.pages=e19567-e19567&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0019567&rft_dat=%3Cgale_plos_%3EA476892101%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1295065371&rft_id=info:pmid/21573167&rft_galeid=A476892101&rft_doaj_id=oai_doaj_org_article_fcead2eb729443c487150f939df9a718&rfr_iscdi=true |