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Magnesium boosts the memory restorative effect of environmental enrichment in Alzheimer's disease mice
Summary Background Environmental enrichment (EE) has been shown to enhance cognitive function in mouse models of Alzheimer's disease (AD). Magnesium‐L‐threonate (MgT) is a compound with a newly discovered effect to rescue learning and memory function in aging and AD mice. Aim To study the addit...
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Published in: | CNS neuroscience & therapeutics 2018-01, Vol.24 (1), p.70-79 |
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creator | Huang, Ying Huang, Xian Zhang, Ling Han, Fang Pang, Ke‐Liang Li, Xue Shen, Jian‐Ying |
description | Summary
Background
Environmental enrichment (EE) has been shown to enhance cognitive function in mouse models of Alzheimer's disease (AD). Magnesium‐L‐threonate (MgT) is a compound with a newly discovered effect to rescue learning and memory function in aging and AD mice.
Aim
To study the additive therapeutic effect of EE combined with MgT (EM) and the potential mechanism underlying the effects.
Materials and Methods
APP/PS1 mice were treated with EE, MgT, or combination of EE and MgT (EM) and compared for restored memory function.
Results
EM was more effective in improving cognition and spatial memory than either treatment alone in either long‐term (12 months, started at 3 months old, which was before disease manifestation) or short‐term (3 months, started at 6 months old, which was after disease manifestation) treatment. The behavioral improvement has coincided with rescue of synaptic contacts in the hippocampal region of the AD mouse brain. Immunoblots also showed that EM but neither single treatment rescued the activity reduction in CaMKII and CREB, two important downstream molecules in the N‐methyl‐D‐aspartate receptor (NMDAR) pathway.
Conclusion
Environmental enrichment and MgT may synergistically improve recognition and spatial memory by reducing synaptic loss and restoring the NMDAR signaling pathway in AD mice, which suggests that combination of EE and MgT may be a novel therapeutic strategy for AD. |
doi_str_mv | 10.1111/cns.12775 |
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Background
Environmental enrichment (EE) has been shown to enhance cognitive function in mouse models of Alzheimer's disease (AD). Magnesium‐L‐threonate (MgT) is a compound with a newly discovered effect to rescue learning and memory function in aging and AD mice.
Aim
To study the additive therapeutic effect of EE combined with MgT (EM) and the potential mechanism underlying the effects.
Materials and Methods
APP/PS1 mice were treated with EE, MgT, or combination of EE and MgT (EM) and compared for restored memory function.
Results
EM was more effective in improving cognition and spatial memory than either treatment alone in either long‐term (12 months, started at 3 months old, which was before disease manifestation) or short‐term (3 months, started at 6 months old, which was after disease manifestation) treatment. The behavioral improvement has coincided with rescue of synaptic contacts in the hippocampal region of the AD mouse brain. Immunoblots also showed that EM but neither single treatment rescued the activity reduction in CaMKII and CREB, two important downstream molecules in the N‐methyl‐D‐aspartate receptor (NMDAR) pathway.
Conclusion
Environmental enrichment and MgT may synergistically improve recognition and spatial memory by reducing synaptic loss and restoring the NMDAR signaling pathway in AD mice, which suggests that combination of EE and MgT may be a novel therapeutic strategy for AD.</description><identifier>ISSN: 1755-5930</identifier><identifier>EISSN: 1755-5949</identifier><identifier>DOI: 10.1111/cns.12775</identifier><identifier>PMID: 29125684</identifier><language>eng</language><publisher>England: John Wiley & Sons, Inc</publisher><subject>Alzheimer Disease - complications ; Alzheimer Disease - genetics ; Alzheimer Disease - pathology ; Alzheimer Disease - therapy ; Alzheimer's disease ; Amyloid beta-Protein Precursor - genetics ; Animal models ; Animals ; APP/PS1 mouse ; Ca2+/calmodulin-dependent protein kinase II ; Calcium-Calmodulin-Dependent Protein Kinase Type 2 - metabolism ; Cognitive ability ; CREB-Binding Protein - metabolism ; Cyclic AMP response element-binding protein ; Disease Models, Animal ; Enrichment ; Environment ; environmental enrichment ; Glutamic acid receptors ; Hippocampus ; Humans ; Learning ; Magnesium ; Magnesium - therapeutic use ; Maze Learning - drug effects ; Maze Learning - physiology ; Memory ; Memory Disorders - etiology ; Memory Disorders - therapy ; Mice ; Mice, Transgenic ; Mutation - genetics ; N-Methyl-D-aspartic acid receptors ; Neurodegenerative diseases ; N‐methyl‐D‐aspartate receptor signaling ; Original ; Presenilin 1 ; Presenilin-1 - genetics ; Receptors, N-Methyl-D-Aspartate - metabolism ; Recognition, Psychology ; Signal transduction ; Signal Transduction - drug effects ; Signal Transduction - genetics ; Spatial memory ; Synapses - drug effects ; Synapses - pathology ; Time Factors</subject><ispartof>CNS neuroscience & therapeutics, 2018-01, Vol.24 (1), p.70-79</ispartof><rights>2017 John Wiley & Sons Ltd</rights><rights>2017 John Wiley & Sons Ltd.</rights><rights>Copyright © 2018 John Wiley & Sons Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4435-a71aab83af1647f387705cb9bda0aa8f7811a24e8381a83e04fb6c929174ba793</citedby><cites>FETCH-LOGICAL-c4435-a71aab83af1647f387705cb9bda0aa8f7811a24e8381a83e04fb6c929174ba793</cites><orcidid>0000-0003-3489-8181 ; 0000-0002-8207-7970</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6489792/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6489792/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,11542,27903,27904,46031,46455,53770,53772</link.rule.ids><linktorsrc>$$Uhttps://onlinelibrary.wiley.com/doi/abs/10.1111%2Fcns.12775$$EView_record_in_Wiley-Blackwell$$FView_record_in_$$GWiley-Blackwell</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29125684$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Huang, Ying</creatorcontrib><creatorcontrib>Huang, Xian</creatorcontrib><creatorcontrib>Zhang, Ling</creatorcontrib><creatorcontrib>Han, Fang</creatorcontrib><creatorcontrib>Pang, Ke‐Liang</creatorcontrib><creatorcontrib>Li, Xue</creatorcontrib><creatorcontrib>Shen, Jian‐Ying</creatorcontrib><title>Magnesium boosts the memory restorative effect of environmental enrichment in Alzheimer's disease mice</title><title>CNS neuroscience & therapeutics</title><addtitle>CNS Neurosci Ther</addtitle><description>Summary
Background
Environmental enrichment (EE) has been shown to enhance cognitive function in mouse models of Alzheimer's disease (AD). Magnesium‐L‐threonate (MgT) is a compound with a newly discovered effect to rescue learning and memory function in aging and AD mice.
Aim
To study the additive therapeutic effect of EE combined with MgT (EM) and the potential mechanism underlying the effects.
Materials and Methods
APP/PS1 mice were treated with EE, MgT, or combination of EE and MgT (EM) and compared for restored memory function.
Results
EM was more effective in improving cognition and spatial memory than either treatment alone in either long‐term (12 months, started at 3 months old, which was before disease manifestation) or short‐term (3 months, started at 6 months old, which was after disease manifestation) treatment. The behavioral improvement has coincided with rescue of synaptic contacts in the hippocampal region of the AD mouse brain. Immunoblots also showed that EM but neither single treatment rescued the activity reduction in CaMKII and CREB, two important downstream molecules in the N‐methyl‐D‐aspartate receptor (NMDAR) pathway.
Conclusion
Environmental enrichment and MgT may synergistically improve recognition and spatial memory by reducing synaptic loss and restoring the NMDAR signaling pathway in AD mice, which suggests that combination of EE and MgT may be a novel therapeutic strategy for AD.</description><subject>Alzheimer Disease - complications</subject><subject>Alzheimer Disease - genetics</subject><subject>Alzheimer Disease - pathology</subject><subject>Alzheimer Disease - therapy</subject><subject>Alzheimer's disease</subject><subject>Amyloid beta-Protein Precursor - genetics</subject><subject>Animal models</subject><subject>Animals</subject><subject>APP/PS1 mouse</subject><subject>Ca2+/calmodulin-dependent protein kinase II</subject><subject>Calcium-Calmodulin-Dependent Protein Kinase Type 2 - metabolism</subject><subject>Cognitive ability</subject><subject>CREB-Binding Protein - metabolism</subject><subject>Cyclic AMP response element-binding protein</subject><subject>Disease Models, Animal</subject><subject>Enrichment</subject><subject>Environment</subject><subject>environmental enrichment</subject><subject>Glutamic acid receptors</subject><subject>Hippocampus</subject><subject>Humans</subject><subject>Learning</subject><subject>Magnesium</subject><subject>Magnesium - therapeutic use</subject><subject>Maze Learning - drug effects</subject><subject>Maze Learning - physiology</subject><subject>Memory</subject><subject>Memory Disorders - etiology</subject><subject>Memory Disorders - therapy</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>Mutation - genetics</subject><subject>N-Methyl-D-aspartic acid receptors</subject><subject>Neurodegenerative diseases</subject><subject>N‐methyl‐D‐aspartate receptor signaling</subject><subject>Original</subject><subject>Presenilin 1</subject><subject>Presenilin-1 - genetics</subject><subject>Receptors, N-Methyl-D-Aspartate - metabolism</subject><subject>Recognition, Psychology</subject><subject>Signal transduction</subject><subject>Signal Transduction - drug effects</subject><subject>Signal Transduction - genetics</subject><subject>Spatial memory</subject><subject>Synapses - drug effects</subject><subject>Synapses - pathology</subject><subject>Time Factors</subject><issn>1755-5930</issn><issn>1755-5949</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kV9PFDEUxRsjEUQf_AKmiQ_Kw8J02pm2LyRkI38S0AfhubnTvWVLZlpsZ9Ysn97CwkZN7Et7019OzrmHkA-sOmTlHNmQD1ktZfOK7DHZNLNGC_16--bVLnmb811VtbXS6g3ZrTWrm1aJPeKu4DZg9tNAuxjzmOm4RDrgENOaJsxjTDD6FVJ0Du1Io6MYVj7FMGAYoS9T8nb5OFAf6En_sEQ_YPqc6cJnhFzEvMV3ZMdBn_H9871Pbk6_Xs_PZ5ffzy7mJ5czKwRvZiAZQKc4ONYK6biSsmpsp7sFVADKScUY1AIVVwwUx0q4rrW6xJGiA6n5Pjne6N5P3YALW2wl6M198gOktYngzd8_wS_NbVyZVigtdV0EvjwLpPhzKvnN4LPFvoeAccqG6ZbXsiyWFfTTP-hdnFIo8Qol21pzJnmhDjaUTTHnhG5rhlXmsT1T2jNP7RX245_ut-RLXQU42gC_fI_r_yuZ-bcfG8nfBdSmJA</recordid><startdate>201801</startdate><enddate>201801</enddate><creator>Huang, Ying</creator><creator>Huang, Xian</creator><creator>Zhang, Ling</creator><creator>Han, Fang</creator><creator>Pang, Ke‐Liang</creator><creator>Li, Xue</creator><creator>Shen, Jian‐Ying</creator><general>John Wiley & Sons, Inc</general><general>John Wiley and Sons Inc</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>7TK</scope><scope>K9.</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-3489-8181</orcidid><orcidid>https://orcid.org/0000-0002-8207-7970</orcidid></search><sort><creationdate>201801</creationdate><title>Magnesium boosts the memory restorative effect of environmental enrichment in Alzheimer's disease mice</title><author>Huang, Ying ; Huang, Xian ; Zhang, Ling ; Han, Fang ; Pang, Ke‐Liang ; Li, Xue ; Shen, Jian‐Ying</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4435-a71aab83af1647f387705cb9bda0aa8f7811a24e8381a83e04fb6c929174ba793</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Alzheimer Disease - complications</topic><topic>Alzheimer Disease - genetics</topic><topic>Alzheimer Disease - pathology</topic><topic>Alzheimer Disease - therapy</topic><topic>Alzheimer's disease</topic><topic>Amyloid beta-Protein Precursor - genetics</topic><topic>Animal models</topic><topic>Animals</topic><topic>APP/PS1 mouse</topic><topic>Ca2+/calmodulin-dependent protein kinase II</topic><topic>Calcium-Calmodulin-Dependent Protein Kinase Type 2 - metabolism</topic><topic>Cognitive ability</topic><topic>CREB-Binding Protein - metabolism</topic><topic>Cyclic AMP response element-binding protein</topic><topic>Disease Models, Animal</topic><topic>Enrichment</topic><topic>Environment</topic><topic>environmental enrichment</topic><topic>Glutamic acid receptors</topic><topic>Hippocampus</topic><topic>Humans</topic><topic>Learning</topic><topic>Magnesium</topic><topic>Magnesium - therapeutic use</topic><topic>Maze Learning - drug effects</topic><topic>Maze Learning - physiology</topic><topic>Memory</topic><topic>Memory Disorders - etiology</topic><topic>Memory Disorders - therapy</topic><topic>Mice</topic><topic>Mice, Transgenic</topic><topic>Mutation - genetics</topic><topic>N-Methyl-D-aspartic acid receptors</topic><topic>Neurodegenerative diseases</topic><topic>N‐methyl‐D‐aspartate receptor signaling</topic><topic>Original</topic><topic>Presenilin 1</topic><topic>Presenilin-1 - genetics</topic><topic>Receptors, N-Methyl-D-Aspartate - metabolism</topic><topic>Recognition, Psychology</topic><topic>Signal transduction</topic><topic>Signal Transduction - drug effects</topic><topic>Signal Transduction - genetics</topic><topic>Spatial memory</topic><topic>Synapses - drug effects</topic><topic>Synapses - pathology</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Huang, Ying</creatorcontrib><creatorcontrib>Huang, Xian</creatorcontrib><creatorcontrib>Zhang, Ling</creatorcontrib><creatorcontrib>Han, Fang</creatorcontrib><creatorcontrib>Pang, Ke‐Liang</creatorcontrib><creatorcontrib>Li, Xue</creatorcontrib><creatorcontrib>Shen, Jian‐Ying</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>CNS neuroscience & therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Huang, Ying</au><au>Huang, Xian</au><au>Zhang, Ling</au><au>Han, Fang</au><au>Pang, Ke‐Liang</au><au>Li, Xue</au><au>Shen, Jian‐Ying</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Magnesium boosts the memory restorative effect of environmental enrichment in Alzheimer's disease mice</atitle><jtitle>CNS neuroscience & therapeutics</jtitle><addtitle>CNS Neurosci Ther</addtitle><date>2018-01</date><risdate>2018</risdate><volume>24</volume><issue>1</issue><spage>70</spage><epage>79</epage><pages>70-79</pages><issn>1755-5930</issn><eissn>1755-5949</eissn><abstract>Summary
Background
Environmental enrichment (EE) has been shown to enhance cognitive function in mouse models of Alzheimer's disease (AD). Magnesium‐L‐threonate (MgT) is a compound with a newly discovered effect to rescue learning and memory function in aging and AD mice.
Aim
To study the additive therapeutic effect of EE combined with MgT (EM) and the potential mechanism underlying the effects.
Materials and Methods
APP/PS1 mice were treated with EE, MgT, or combination of EE and MgT (EM) and compared for restored memory function.
Results
EM was more effective in improving cognition and spatial memory than either treatment alone in either long‐term (12 months, started at 3 months old, which was before disease manifestation) or short‐term (3 months, started at 6 months old, which was after disease manifestation) treatment. The behavioral improvement has coincided with rescue of synaptic contacts in the hippocampal region of the AD mouse brain. Immunoblots also showed that EM but neither single treatment rescued the activity reduction in CaMKII and CREB, two important downstream molecules in the N‐methyl‐D‐aspartate receptor (NMDAR) pathway.
Conclusion
Environmental enrichment and MgT may synergistically improve recognition and spatial memory by reducing synaptic loss and restoring the NMDAR signaling pathway in AD mice, which suggests that combination of EE and MgT may be a novel therapeutic strategy for AD.</abstract><cop>England</cop><pub>John Wiley & Sons, Inc</pub><pmid>29125684</pmid><doi>10.1111/cns.12775</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-3489-8181</orcidid><orcidid>https://orcid.org/0000-0002-8207-7970</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Alzheimer Disease - complications Alzheimer Disease - genetics Alzheimer Disease - pathology Alzheimer Disease - therapy Alzheimer's disease Amyloid beta-Protein Precursor - genetics Animal models Animals APP/PS1 mouse Ca2+/calmodulin-dependent protein kinase II Calcium-Calmodulin-Dependent Protein Kinase Type 2 - metabolism Cognitive ability CREB-Binding Protein - metabolism Cyclic AMP response element-binding protein Disease Models, Animal Enrichment Environment environmental enrichment Glutamic acid receptors Hippocampus Humans Learning Magnesium Magnesium - therapeutic use Maze Learning - drug effects Maze Learning - physiology Memory Memory Disorders - etiology Memory Disorders - therapy Mice Mice, Transgenic Mutation - genetics N-Methyl-D-aspartic acid receptors Neurodegenerative diseases N‐methyl‐D‐aspartate receptor signaling Original Presenilin 1 Presenilin-1 - genetics Receptors, N-Methyl-D-Aspartate - metabolism Recognition, Psychology Signal transduction Signal Transduction - drug effects Signal Transduction - genetics Spatial memory Synapses - drug effects Synapses - pathology Time Factors |
title | Magnesium boosts the memory restorative effect of environmental enrichment in Alzheimer's disease mice |
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