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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
Main Authors: Huang, Ying, Huang, Xian, Zhang, Ling, Han, Fang, Pang, Ke‐Liang, Li, Xue, Shen, Jian‐Ying
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container_title CNS neuroscience & therapeutics
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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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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 &amp; 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 &amp; therapeutics, 2018-01, Vol.24 (1), p.70-79</ispartof><rights>2017 John Wiley &amp; Sons Ltd</rights><rights>2017 John Wiley &amp; Sons Ltd.</rights><rights>Copyright © 2018 John Wiley &amp; 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 &amp; 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 &amp; 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 &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>CNS neuroscience &amp; 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 &amp; 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 &amp; 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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