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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Synapse (New York, N.Y.) N.Y.), 2013-12, Vol.67 (12), p.856-864
Hauptverfasser: Ding, Juan, Xi, Yuan-Di, Zhang, Dan-Di, Zhao, Xia, Liu, Jin-Meng, Li, Chao-Qun, Han, Jing, Xiao, Rong
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 864
container_issue 12
container_start_page 856
container_title Synapse (New York, N.Y.)
container_volume 67
creator Ding, Juan
Xi, Yuan-Di
Zhang, Dan-Di
Zhao, Xia
Liu, Jin-Meng
Li, Chao-Qun
Han, Jing
Xiao, Rong
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.
doi_str_mv 10.1002/syn.21692
format Article
fullrecord <record><control><sourceid>istex_pubme</sourceid><recordid>TN_cdi_pubmed_primary_23766238</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>ark_67375_WNG_0G5276BD_2</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3292-8c96096a39075a58b46715487c0fa3836f9d7026392daf94672e25bd8e4e259f3</originalsourceid><addsrcrecordid>eNo9kEtOwzAURS0EgvIZsAHkDbh17MSfId-ChGBQEGJkObGDDIlT2QmQHbAeFsKaMC0wek-697zPBeAww9MMYzKLo5-SjEmyASYZlgIRKtkmmGAhOMpzznbAbozPGGOa4Xwb7BDKGSNUTMDHohtLqz10sasb_dp5C3VrG9cF3dsIvz6RbsemcwZmKCfIeTNU1sDG6uCdf4LaG9jatgsjNLZ2leuh8zDBEZYjXIaut1X_Y0xH6mXvKhj7MFT9EOyKrQef9M7vg61aN9Ee_NY9cH9xfnd6ia5v51enx9eookQSJCrJsGSaSswLXYgyZzwrcsErXGsqKKul4ZgwKonRtUwqsaQojbB5qrKme-BoPXc5lK01ahlcq8Oo_iJJhtna8OYaO_7rGVY_Wav0hlplrRaPN6smEWhNuNjb939ChxfFOOWFeriZKzwvCGcnZ2nRN6trgl8</addsrcrecordid><sourcetype>Index Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Soybean isoflavone ameliorates β-amyloid 1-42-induced learning and memory deficit in rats by protecting synaptic structure and function</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Ding, Juan ; Xi, Yuan-Di ; Zhang, Dan-Di ; Zhao, Xia ; Liu, Jin-Meng ; Li, Chao-Qun ; Han, Jing ; Xiao, Rong</creator><creatorcontrib>Ding, Juan ; Xi, Yuan-Di ; Zhang, Dan-Di ; Zhao, Xia ; Liu, Jin-Meng ; Li, Chao-Qun ; Han, Jing ; Xiao, Rong</creatorcontrib><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><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>
fulltext fulltext
identifier ISSN: 0887-4476
ispartof Synapse (New York, N.Y.), 2013-12, Vol.67 (12), p.856-864
issn 0887-4476
1098-2396
language eng
recordid cdi_pubmed_primary_23766238
source MEDLINE; Wiley Online Library Journals Frontfile Complete
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-22T03%3A50%3A23IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-istex_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Soybean%20isoflavone%20ameliorates%20%CE%B2-amyloid%201-42-induced%20learning%20and%20memory%20deficit%20in%20rats%20by%20protecting%20synaptic%20structure%20and%20function&rft.jtitle=Synapse%20(New%20York,%20N.Y.)&rft.au=Ding,%20Juan&rft.date=2013-12&rft.volume=67&rft.issue=12&rft.spage=856&rft.epage=864&rft.pages=856-864&rft.issn=0887-4476&rft.eissn=1098-2396&rft_id=info:doi/10.1002/syn.21692&rft_dat=%3Cistex_pubme%3Eark_67375_WNG_0G5276BD_2%3C/istex_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/23766238&rfr_iscdi=true