Soybean isoflavone ameliorates β-amyloid 1-42-induced learning and memory deficit in rats by protecting synaptic structure and function
ABSTRACT This research aims to investigate whether soybean isoflavone (SIF) could alleviate the learning and memory deficit induced by β‐amyloid peptides 1‐42 (Aβ1‐42) by protecting the synapses of rats. Adult male Wistar rats were randomly allocated to the following groups: (1) control group; (2) A...
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Veröffentlicht in: | Synapse (New York, N.Y.) N.Y.), 2013-12, Vol.67 (12), p.856-864 |
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creator | Ding, Juan Xi, Yuan-Di Zhang, Dan-Di Zhao, Xia Liu, Jin-Meng Li, Chao-Qun Han, Jing Xiao, Rong |
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This research aims to investigate whether soybean isoflavone (SIF) could alleviate the learning and memory deficit induced by β‐amyloid peptides 1‐42 (Aβ1‐42) by protecting the synapses of rats. Adult male Wistar rats were randomly allocated to the following groups: (1) control group; (2) Aβ1‐42 group; (3) SIF group; (4) SIF + Aβ1‐42 group (SIF pretreatment group) according to body weight. The 80 mg/kg/day of SIF was administered orally by gavage to the rats in SIF and SIF+Aβ1‐42 groups. Aβ1‐42 was injected into the lateral cerebral ventricle of rats in Aβ1‐42 and SIF+Aβ1‐42 groups. The ability of learning and memory, ultramicrostructure of hippocampal synapses, and expression of synaptic related proteins were investigated. The Morris water maze results showed the escape latency and total distance were decreased in the rats of SIF pretreatment group compared to the rats in Aβ1‐42 group. Furthermore, SIF pretreatment could alleviate the synaptic structural damage and antagonize the down‐regulation expressions of below proteins induced by Aβ1‐42: (1) mRNA and protein of the synaptophysin and postsynaptic density protein 95 (PSD‐95); (2) protein of calmodulin (CaM), Ca2+/calmodulin‐dependent protein kinase II (CaMK II), and cAMP response element binding protein (CREB); (3) phosphorylation levels of CaMK II and CREB (pCAMK II, pCREB). These results suggested that SIF pretreatment could ameliorate the impairment of learning and memory ability in rats induced by Aβ1‐42, and its mechanism might be associated with the protection of synaptic plasticity by improving the synaptic structure and regulating the synaptic related proteins. Synapse 67:856–864, 2013. © 2013 Wiley Periodicals, Inc. |
doi_str_mv | 10.1002/syn.21692 |
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This research aims to investigate whether soybean isoflavone (SIF) could alleviate the learning and memory deficit induced by β‐amyloid peptides 1‐42 (Aβ1‐42) by protecting the synapses of rats. Adult male Wistar rats were randomly allocated to the following groups: (1) control group; (2) Aβ1‐42 group; (3) SIF group; (4) SIF + Aβ1‐42 group (SIF pretreatment group) according to body weight. The 80 mg/kg/day of SIF was administered orally by gavage to the rats in SIF and SIF+Aβ1‐42 groups. Aβ1‐42 was injected into the lateral cerebral ventricle of rats in Aβ1‐42 and SIF+Aβ1‐42 groups. The ability of learning and memory, ultramicrostructure of hippocampal synapses, and expression of synaptic related proteins were investigated. The Morris water maze results showed the escape latency and total distance were decreased in the rats of SIF pretreatment group compared to the rats in Aβ1‐42 group. Furthermore, SIF pretreatment could alleviate the synaptic structural damage and antagonize the down‐regulation expressions of below proteins induced by Aβ1‐42: (1) mRNA and protein of the synaptophysin and postsynaptic density protein 95 (PSD‐95); (2) protein of calmodulin (CaM), Ca2+/calmodulin‐dependent protein kinase II (CaMK II), and cAMP response element binding protein (CREB); (3) phosphorylation levels of CaMK II and CREB (pCAMK II, pCREB). These results suggested that SIF pretreatment could ameliorate the impairment of learning and memory ability in rats induced by Aβ1‐42, and its mechanism might be associated with the protection of synaptic plasticity by improving the synaptic structure and regulating the synaptic related proteins. Synapse 67:856–864, 2013. © 2013 Wiley Periodicals, Inc.</description><identifier>ISSN: 0887-4476</identifier><identifier>EISSN: 1098-2396</identifier><identifier>DOI: 10.1002/syn.21692</identifier><identifier>PMID: 23766238</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Amyloid beta-Peptides - toxicity ; Animals ; Calcium-Calmodulin-Dependent Protein Kinase Type 2 - genetics ; Calcium-Calmodulin-Dependent Protein Kinase Type 2 - metabolism ; Calmodulin - genetics ; Calmodulin - metabolism ; Cyclic AMP Response Element-Binding Protein - genetics ; Cyclic AMP Response Element-Binding Protein - metabolism ; Disks Large Homolog 4 Protein ; Glycine max - chemistry ; Hippocampus - cytology ; Hippocampus - drug effects ; Hippocampus - metabolism ; Hippocampus - physiology ; Intracellular Signaling Peptides and Proteins - genetics ; Intracellular Signaling Peptides and Proteins - metabolism ; Isoflavones - pharmacology ; Isoflavones - therapeutic use ; learning and memory ; Male ; Maze Learning - drug effects ; Membrane Proteins - genetics ; Membrane Proteins - metabolism ; Memory - drug effects ; Memory Disorders - chemically induced ; Memory Disorders - drug therapy ; neuroprotection ; Peptide Fragments - toxicity ; Phosphorylation ; Phytotherapy ; Plant Extracts - pharmacology ; Plant Extracts - therapeutic use ; Rats ; Rats, Wistar ; Reaction Time ; soybean isoflavone ; Synapses - drug effects ; Synapses - metabolism ; Synapses - physiology ; Synapses - ultrastructure ; synaptic dysfunction ; Transcription, Genetic</subject><ispartof>Synapse (New York, N.Y.), 2013-12, Vol.67 (12), p.856-864</ispartof><rights>Copyright © 2013 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3292-8c96096a39075a58b46715487c0fa3836f9d7026392daf94672e25bd8e4e259f3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fsyn.21692$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fsyn.21692$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23766238$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ding, Juan</creatorcontrib><creatorcontrib>Xi, Yuan-Di</creatorcontrib><creatorcontrib>Zhang, Dan-Di</creatorcontrib><creatorcontrib>Zhao, Xia</creatorcontrib><creatorcontrib>Liu, Jin-Meng</creatorcontrib><creatorcontrib>Li, Chao-Qun</creatorcontrib><creatorcontrib>Han, Jing</creatorcontrib><creatorcontrib>Xiao, Rong</creatorcontrib><title>Soybean isoflavone ameliorates β-amyloid 1-42-induced learning and memory deficit in rats by protecting synaptic structure and function</title><title>Synapse (New York, N.Y.)</title><addtitle>Synapse</addtitle><description>ABSTRACT
This research aims to investigate whether soybean isoflavone (SIF) could alleviate the learning and memory deficit induced by β‐amyloid peptides 1‐42 (Aβ1‐42) by protecting the synapses of rats. Adult male Wistar rats were randomly allocated to the following groups: (1) control group; (2) Aβ1‐42 group; (3) SIF group; (4) SIF + Aβ1‐42 group (SIF pretreatment group) according to body weight. The 80 mg/kg/day of SIF was administered orally by gavage to the rats in SIF and SIF+Aβ1‐42 groups. Aβ1‐42 was injected into the lateral cerebral ventricle of rats in Aβ1‐42 and SIF+Aβ1‐42 groups. The ability of learning and memory, ultramicrostructure of hippocampal synapses, and expression of synaptic related proteins were investigated. The Morris water maze results showed the escape latency and total distance were decreased in the rats of SIF pretreatment group compared to the rats in Aβ1‐42 group. Furthermore, SIF pretreatment could alleviate the synaptic structural damage and antagonize the down‐regulation expressions of below proteins induced by Aβ1‐42: (1) mRNA and protein of the synaptophysin and postsynaptic density protein 95 (PSD‐95); (2) protein of calmodulin (CaM), Ca2+/calmodulin‐dependent protein kinase II (CaMK II), and cAMP response element binding protein (CREB); (3) phosphorylation levels of CaMK II and CREB (pCAMK II, pCREB). These results suggested that SIF pretreatment could ameliorate the impairment of learning and memory ability in rats induced by Aβ1‐42, and its mechanism might be associated with the protection of synaptic plasticity by improving the synaptic structure and regulating the synaptic related proteins. Synapse 67:856–864, 2013. © 2013 Wiley Periodicals, Inc.</description><subject>Amyloid beta-Peptides - toxicity</subject><subject>Animals</subject><subject>Calcium-Calmodulin-Dependent Protein Kinase Type 2 - genetics</subject><subject>Calcium-Calmodulin-Dependent Protein Kinase Type 2 - metabolism</subject><subject>Calmodulin - genetics</subject><subject>Calmodulin - metabolism</subject><subject>Cyclic AMP Response Element-Binding Protein - genetics</subject><subject>Cyclic AMP Response Element-Binding Protein - metabolism</subject><subject>Disks Large Homolog 4 Protein</subject><subject>Glycine max - chemistry</subject><subject>Hippocampus - cytology</subject><subject>Hippocampus - drug effects</subject><subject>Hippocampus - metabolism</subject><subject>Hippocampus - physiology</subject><subject>Intracellular Signaling Peptides and Proteins - genetics</subject><subject>Intracellular Signaling Peptides and Proteins - metabolism</subject><subject>Isoflavones - pharmacology</subject><subject>Isoflavones - therapeutic use</subject><subject>learning and memory</subject><subject>Male</subject><subject>Maze Learning - drug effects</subject><subject>Membrane Proteins - genetics</subject><subject>Membrane Proteins - metabolism</subject><subject>Memory - drug effects</subject><subject>Memory Disorders - chemically induced</subject><subject>Memory Disorders - drug therapy</subject><subject>neuroprotection</subject><subject>Peptide Fragments - toxicity</subject><subject>Phosphorylation</subject><subject>Phytotherapy</subject><subject>Plant Extracts - pharmacology</subject><subject>Plant Extracts - therapeutic use</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Reaction Time</subject><subject>soybean isoflavone</subject><subject>Synapses - drug effects</subject><subject>Synapses - metabolism</subject><subject>Synapses - physiology</subject><subject>Synapses - ultrastructure</subject><subject>synaptic dysfunction</subject><subject>Transcription, Genetic</subject><issn>0887-4476</issn><issn>1098-2396</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kEtOwzAURS0EgvIZsAHkDbh17MSfId-ChGBQEGJkObGDDIlT2QmQHbAeFsKaMC0wek-697zPBeAww9MMYzKLo5-SjEmyASYZlgIRKtkmmGAhOMpzznbAbozPGGOa4Xwb7BDKGSNUTMDHohtLqz10sasb_dp5C3VrG9cF3dsIvz6RbsemcwZmKCfIeTNU1sDG6uCdf4LaG9jatgsjNLZ2leuh8zDBEZYjXIaut1X_Y0xH6mXvKhj7MFT9EOyKrQef9M7vg61aN9Ee_NY9cH9xfnd6ia5v51enx9eookQSJCrJsGSaSswLXYgyZzwrcsErXGsqKKul4ZgwKonRtUwqsaQojbB5qrKme-BoPXc5lK01ahlcq8Oo_iJJhtna8OYaO_7rGVY_Wav0hlplrRaPN6smEWhNuNjb939ChxfFOOWFeriZKzwvCGcnZ2nRN6trgl8</recordid><startdate>201312</startdate><enddate>201312</enddate><creator>Ding, Juan</creator><creator>Xi, Yuan-Di</creator><creator>Zhang, Dan-Di</creator><creator>Zhao, Xia</creator><creator>Liu, Jin-Meng</creator><creator>Li, Chao-Qun</creator><creator>Han, Jing</creator><creator>Xiao, Rong</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>201312</creationdate><title>Soybean isoflavone ameliorates β-amyloid 1-42-induced learning and memory deficit in rats by protecting synaptic structure and function</title><author>Ding, Juan ; Xi, Yuan-Di ; Zhang, Dan-Di ; Zhao, Xia ; Liu, Jin-Meng ; Li, Chao-Qun ; Han, Jing ; Xiao, Rong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3292-8c96096a39075a58b46715487c0fa3836f9d7026392daf94672e25bd8e4e259f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Amyloid beta-Peptides - toxicity</topic><topic>Animals</topic><topic>Calcium-Calmodulin-Dependent Protein Kinase Type 2 - genetics</topic><topic>Calcium-Calmodulin-Dependent Protein Kinase Type 2 - metabolism</topic><topic>Calmodulin - genetics</topic><topic>Calmodulin - metabolism</topic><topic>Cyclic AMP Response Element-Binding Protein - genetics</topic><topic>Cyclic AMP Response Element-Binding Protein - metabolism</topic><topic>Disks Large Homolog 4 Protein</topic><topic>Glycine max - chemistry</topic><topic>Hippocampus - cytology</topic><topic>Hippocampus - drug effects</topic><topic>Hippocampus - metabolism</topic><topic>Hippocampus - physiology</topic><topic>Intracellular Signaling Peptides and Proteins - genetics</topic><topic>Intracellular Signaling Peptides and Proteins - metabolism</topic><topic>Isoflavones - pharmacology</topic><topic>Isoflavones - therapeutic use</topic><topic>learning and memory</topic><topic>Male</topic><topic>Maze Learning - drug effects</topic><topic>Membrane Proteins - genetics</topic><topic>Membrane Proteins - metabolism</topic><topic>Memory - drug effects</topic><topic>Memory Disorders - chemically induced</topic><topic>Memory Disorders - drug therapy</topic><topic>neuroprotection</topic><topic>Peptide Fragments - toxicity</topic><topic>Phosphorylation</topic><topic>Phytotherapy</topic><topic>Plant Extracts - pharmacology</topic><topic>Plant Extracts - therapeutic use</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Reaction Time</topic><topic>soybean isoflavone</topic><topic>Synapses - drug effects</topic><topic>Synapses - metabolism</topic><topic>Synapses - physiology</topic><topic>Synapses - ultrastructure</topic><topic>synaptic dysfunction</topic><topic>Transcription, Genetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ding, Juan</creatorcontrib><creatorcontrib>Xi, Yuan-Di</creatorcontrib><creatorcontrib>Zhang, Dan-Di</creatorcontrib><creatorcontrib>Zhao, Xia</creatorcontrib><creatorcontrib>Liu, Jin-Meng</creatorcontrib><creatorcontrib>Li, Chao-Qun</creatorcontrib><creatorcontrib>Han, Jing</creatorcontrib><creatorcontrib>Xiao, Rong</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Synapse (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ding, Juan</au><au>Xi, Yuan-Di</au><au>Zhang, Dan-Di</au><au>Zhao, Xia</au><au>Liu, Jin-Meng</au><au>Li, Chao-Qun</au><au>Han, Jing</au><au>Xiao, Rong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Soybean isoflavone ameliorates β-amyloid 1-42-induced learning and memory deficit in rats by protecting synaptic structure and function</atitle><jtitle>Synapse (New York, N.Y.)</jtitle><addtitle>Synapse</addtitle><date>2013-12</date><risdate>2013</risdate><volume>67</volume><issue>12</issue><spage>856</spage><epage>864</epage><pages>856-864</pages><issn>0887-4476</issn><eissn>1098-2396</eissn><abstract>ABSTRACT
This research aims to investigate whether soybean isoflavone (SIF) could alleviate the learning and memory deficit induced by β‐amyloid peptides 1‐42 (Aβ1‐42) by protecting the synapses of rats. Adult male Wistar rats were randomly allocated to the following groups: (1) control group; (2) Aβ1‐42 group; (3) SIF group; (4) SIF + Aβ1‐42 group (SIF pretreatment group) according to body weight. The 80 mg/kg/day of SIF was administered orally by gavage to the rats in SIF and SIF+Aβ1‐42 groups. Aβ1‐42 was injected into the lateral cerebral ventricle of rats in Aβ1‐42 and SIF+Aβ1‐42 groups. The ability of learning and memory, ultramicrostructure of hippocampal synapses, and expression of synaptic related proteins were investigated. The Morris water maze results showed the escape latency and total distance were decreased in the rats of SIF pretreatment group compared to the rats in Aβ1‐42 group. Furthermore, SIF pretreatment could alleviate the synaptic structural damage and antagonize the down‐regulation expressions of below proteins induced by Aβ1‐42: (1) mRNA and protein of the synaptophysin and postsynaptic density protein 95 (PSD‐95); (2) protein of calmodulin (CaM), Ca2+/calmodulin‐dependent protein kinase II (CaMK II), and cAMP response element binding protein (CREB); (3) phosphorylation levels of CaMK II and CREB (pCAMK II, pCREB). These results suggested that SIF pretreatment could ameliorate the impairment of learning and memory ability in rats induced by Aβ1‐42, and its mechanism might be associated with the protection of synaptic plasticity by improving the synaptic structure and regulating the synaptic related proteins. Synapse 67:856–864, 2013. © 2013 Wiley Periodicals, Inc.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>23766238</pmid><doi>10.1002/syn.21692</doi><tpages>9</tpages></addata></record> |
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subjects | Amyloid beta-Peptides - toxicity Animals Calcium-Calmodulin-Dependent Protein Kinase Type 2 - genetics Calcium-Calmodulin-Dependent Protein Kinase Type 2 - metabolism Calmodulin - genetics Calmodulin - metabolism Cyclic AMP Response Element-Binding Protein - genetics Cyclic AMP Response Element-Binding Protein - metabolism Disks Large Homolog 4 Protein Glycine max - chemistry Hippocampus - cytology Hippocampus - drug effects Hippocampus - metabolism Hippocampus - physiology Intracellular Signaling Peptides and Proteins - genetics Intracellular Signaling Peptides and Proteins - metabolism Isoflavones - pharmacology Isoflavones - therapeutic use learning and memory Male Maze Learning - drug effects Membrane Proteins - genetics Membrane Proteins - metabolism Memory - drug effects Memory Disorders - chemically induced Memory Disorders - drug therapy neuroprotection Peptide Fragments - toxicity Phosphorylation Phytotherapy Plant Extracts - pharmacology Plant Extracts - therapeutic use Rats Rats, Wistar Reaction Time soybean isoflavone Synapses - drug effects Synapses - metabolism Synapses - physiology Synapses - ultrastructure synaptic dysfunction Transcription, Genetic |
title | Soybean isoflavone ameliorates β-amyloid 1-42-induced learning and memory deficit in rats by protecting synaptic structure and function |
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