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A novel trimeric peptide, Neuropep‐1‐stimulating brain‐derived neurotrophic factor expression in rat brain improves spatial learning and memory as measured by the Y‐maze and Morris water maze
J. Neurochem. (2011) 116, 205–216. Abundant studies have shown possible links between low levels of brain‐derived neurotrophic factor (BDNF) and neurological diseases such as Alzheimer’s disease, Parkinson’s disease, and depression, as well as stress and anxiety; therefore, BDNF could be a therapeut...
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description | J. Neurochem. (2011) 116, 205–216.
Abundant studies have shown possible links between low levels of brain‐derived neurotrophic factor (BDNF) and neurological diseases such as Alzheimer’s disease, Parkinson’s disease, and depression, as well as stress and anxiety; therefore, BDNF could be a therapeutic target for neurological disorders. In the present study, a positional scanning‐synthetic peptide combinatorial library was utilized to identify a peptide modulator of BDNF expression in the hippocampal neuronal cell line, H19‐7. A novel tripeptide (Neuropep‐1) induced a significant increase of BDNF mRNA and protein levels in H19‐7 cells. Pre‐treatment of TrkB inhibitor (K252a) did not block Neuropep‐1‐induced BDNF up‐regulation. These results indicate that Neuropep‐1 may up‐regulate BDNF expression that might be independent of the TrkB receptor pathway. Tail vein injection of Neuropep‐1 significantly up‐regulated BDNF expression, TrkB phosphorylation, and its downstream signals including activation of Akt, ERK, and cAMP response element binding in the rat hippocampus. To evaluate improvement of spatial learning and memory (SLM) by Neuropep‐1‐induced BDNF up‐regulation, the Y‐maze and Morris water maze tests were performed. These results showed Neuropep‐1 injection improved SLM performance with increase of BDNF and TrkB expression, activation of TrkB downstream signals in rat hippocampus compared with the control group. However, phosphorylation levels of TrkB were not changed when it was normalized to the level of TrkB expression. The difference on TrkB phosphorylation in Neuropep‐1‐injected rats may be affected by behavioral tests. These results suggest that Neuropep‐1 may improve SLM via activation of the BDNF/TrkB signaling pathway in the rat hippocampus. Therefore, our findings represent that Neuropep‐1 might be a potential candidate for treatment of learning and memory disorders as well as neurological diseases involving the abnormal expression of BDNF. |
doi_str_mv | 10.1111/j.1471-4159.2010.07078.x |
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Abundant studies have shown possible links between low levels of brain‐derived neurotrophic factor (BDNF) and neurological diseases such as Alzheimer’s disease, Parkinson’s disease, and depression, as well as stress and anxiety; therefore, BDNF could be a therapeutic target for neurological disorders. In the present study, a positional scanning‐synthetic peptide combinatorial library was utilized to identify a peptide modulator of BDNF expression in the hippocampal neuronal cell line, H19‐7. A novel tripeptide (Neuropep‐1) induced a significant increase of BDNF mRNA and protein levels in H19‐7 cells. Pre‐treatment of TrkB inhibitor (K252a) did not block Neuropep‐1‐induced BDNF up‐regulation. These results indicate that Neuropep‐1 may up‐regulate BDNF expression that might be independent of the TrkB receptor pathway. Tail vein injection of Neuropep‐1 significantly up‐regulated BDNF expression, TrkB phosphorylation, and its downstream signals including activation of Akt, ERK, and cAMP response element binding in the rat hippocampus. To evaluate improvement of spatial learning and memory (SLM) by Neuropep‐1‐induced BDNF up‐regulation, the Y‐maze and Morris water maze tests were performed. These results showed Neuropep‐1 injection improved SLM performance with increase of BDNF and TrkB expression, activation of TrkB downstream signals in rat hippocampus compared with the control group. However, phosphorylation levels of TrkB were not changed when it was normalized to the level of TrkB expression. The difference on TrkB phosphorylation in Neuropep‐1‐injected rats may be affected by behavioral tests. These results suggest that Neuropep‐1 may improve SLM via activation of the BDNF/TrkB signaling pathway in the rat hippocampus. Therefore, our findings represent that Neuropep‐1 might be a potential candidate for treatment of learning and memory disorders as well as neurological diseases involving the abnormal expression of BDNF.</description><identifier>ISSN: 0022-3042</identifier><identifier>EISSN: 1471-4159</identifier><identifier>DOI: 10.1111/j.1471-4159.2010.07078.x</identifier><identifier>PMID: 21044076</identifier><identifier>CODEN: JONRA9</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adult and adolescent clinical studies ; AKT protein ; Alzheimer's disease ; Animals ; Anxiety ; Biological and medical sciences ; Brain Chemistry - physiology ; Brain-derived neurotrophic factor ; Brain-Derived Neurotrophic Factor - administration & dosage ; Brain-Derived Neurotrophic Factor - biosynthesis ; Brain-Derived Neurotrophic Factor - physiology ; Cell Line ; Combinatorial libraries ; cortex ; Cyclic AMP ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases ; Depression ; Extracellular signal-regulated kinase ; Hippocampus ; Hippocampus - metabolism ; Hippocampus - physiology ; Learning ; Male ; Maze Learning - physiology ; Medical sciences ; Memory ; Memory - physiology ; Movement disorders ; mRNA ; Neurochemistry ; Neurodegenerative diseases ; Neurological diseases ; Neurology ; Neuromodulation ; Neuropeptides - administration & dosage ; Neuropeptides - chemistry ; Neuropeptides - physiology ; Oligopeptides - chemistry ; Oligopeptides - physiology ; Organic mental disorders. Neuropsychology ; Parkinson's disease ; Peptide Library ; Peptides ; Phosphorylation ; Protein Multimerization - physiology ; Psychology. Psychoanalysis. Psychiatry ; Psychopathology. Psychiatry ; Rats ; Rats, Sprague-Dawley ; Receptor, trkB - metabolism ; Receptor, trkB - physiology ; Regulatory sequences ; Rodents ; Signal transduction ; Signal Transduction - physiology ; Spatial Behavior - physiology ; Spatial discrimination learning ; spatial memory ; Stress ; TrkB receptors ; Veins</subject><ispartof>Journal of neurochemistry, 2011-01, Vol.116 (2), p.205-216</ispartof><rights>2010 The Authors. Journal of Neurochemistry © 2010 International Society for Neurochemistry</rights><rights>2015 INIST-CNRS</rights><rights>2010 The Authors. Journal of Neurochemistry © 2010 International Society for Neurochemistry.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4088-ae67ec8627e4411a63c76f115265c9f0f6dfa916e4422101ed2a2e67914666013</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23790991$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21044076$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shin, Min Kyoo</creatorcontrib><creatorcontrib>Kim, Hong Gi</creatorcontrib><creatorcontrib>Kim, Kil Lyong</creatorcontrib><title>A novel trimeric peptide, Neuropep‐1‐stimulating brain‐derived neurotrophic factor expression in rat brain improves spatial learning and memory as measured by the Y‐maze and Morris water maze</title><title>Journal of neurochemistry</title><addtitle>J Neurochem</addtitle><description>J. Neurochem. (2011) 116, 205–216.
Abundant studies have shown possible links between low levels of brain‐derived neurotrophic factor (BDNF) and neurological diseases such as Alzheimer’s disease, Parkinson’s disease, and depression, as well as stress and anxiety; therefore, BDNF could be a therapeutic target for neurological disorders. In the present study, a positional scanning‐synthetic peptide combinatorial library was utilized to identify a peptide modulator of BDNF expression in the hippocampal neuronal cell line, H19‐7. A novel tripeptide (Neuropep‐1) induced a significant increase of BDNF mRNA and protein levels in H19‐7 cells. Pre‐treatment of TrkB inhibitor (K252a) did not block Neuropep‐1‐induced BDNF up‐regulation. These results indicate that Neuropep‐1 may up‐regulate BDNF expression that might be independent of the TrkB receptor pathway. Tail vein injection of Neuropep‐1 significantly up‐regulated BDNF expression, TrkB phosphorylation, and its downstream signals including activation of Akt, ERK, and cAMP response element binding in the rat hippocampus. To evaluate improvement of spatial learning and memory (SLM) by Neuropep‐1‐induced BDNF up‐regulation, the Y‐maze and Morris water maze tests were performed. These results showed Neuropep‐1 injection improved SLM performance with increase of BDNF and TrkB expression, activation of TrkB downstream signals in rat hippocampus compared with the control group. However, phosphorylation levels of TrkB were not changed when it was normalized to the level of TrkB expression. The difference on TrkB phosphorylation in Neuropep‐1‐injected rats may be affected by behavioral tests. These results suggest that Neuropep‐1 may improve SLM via activation of the BDNF/TrkB signaling pathway in the rat hippocampus. Therefore, our findings represent that Neuropep‐1 might be a potential candidate for treatment of learning and memory disorders as well as neurological diseases involving the abnormal expression of BDNF.</description><subject>Adult and adolescent clinical studies</subject><subject>AKT protein</subject><subject>Alzheimer's disease</subject><subject>Animals</subject><subject>Anxiety</subject><subject>Biological and medical sciences</subject><subject>Brain Chemistry - physiology</subject><subject>Brain-derived neurotrophic factor</subject><subject>Brain-Derived Neurotrophic Factor - administration & dosage</subject><subject>Brain-Derived Neurotrophic Factor - biosynthesis</subject><subject>Brain-Derived Neurotrophic Factor - physiology</subject><subject>Cell Line</subject><subject>Combinatorial libraries</subject><subject>cortex</subject><subject>Cyclic AMP</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>Depression</subject><subject>Extracellular signal-regulated kinase</subject><subject>Hippocampus</subject><subject>Hippocampus - metabolism</subject><subject>Hippocampus - physiology</subject><subject>Learning</subject><subject>Male</subject><subject>Maze Learning - physiology</subject><subject>Medical sciences</subject><subject>Memory</subject><subject>Memory - physiology</subject><subject>Movement disorders</subject><subject>mRNA</subject><subject>Neurochemistry</subject><subject>Neurodegenerative diseases</subject><subject>Neurological diseases</subject><subject>Neurology</subject><subject>Neuromodulation</subject><subject>Neuropeptides - administration & dosage</subject><subject>Neuropeptides - chemistry</subject><subject>Neuropeptides - physiology</subject><subject>Oligopeptides - chemistry</subject><subject>Oligopeptides - physiology</subject><subject>Organic mental disorders. Neuropsychology</subject><subject>Parkinson's disease</subject><subject>Peptide Library</subject><subject>Peptides</subject><subject>Phosphorylation</subject><subject>Protein Multimerization - physiology</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopathology. Psychiatry</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptor, trkB - metabolism</subject><subject>Receptor, trkB - physiology</subject><subject>Regulatory sequences</subject><subject>Rodents</subject><subject>Signal transduction</subject><subject>Signal Transduction - physiology</subject><subject>Spatial Behavior - physiology</subject><subject>Spatial discrimination learning</subject><subject>spatial memory</subject><subject>Stress</subject><subject>TrkB receptors</subject><subject>Veins</subject><issn>0022-3042</issn><issn>1471-4159</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNqFks9u1DAQxiMEoqXwCshCQr2wi8dxnOTAoVrxV6Vc4MDJmk0m1KvECXbS7nLiEXgr3oMnYdJdisSFSFbsmd981ni-JBEgl8Df880SdA4LDVm5VJKjMpd5sdzeSY5vE3eTYymVWqRSq6PkQYwbKcFoA_eTIwVSa5mb4-TnmfD9FbViDK6j4Cox0DC6mp6JC5pCz6df338Arzi6bmpxdP6LWAd0nmM1V1xRLfyMjkxfskCD1dgHQdshUIyu98J5EXDcVwnXDYFvjCIOLIataAmDn1XR16Kjrg87gZF3GKfA4uudGC9JfOb7OvxGN9j7PgQXxTWOFMQcfZjca7CN9OjwP0k-vXr5cfVmcf7h9dvV2fmi0rIoFkgmp6owKietAdCkVW4agEyZrCob2Zi6wRIMZxU_ElCtUHFNCdoYIyE9SU73utzE14niaDsXK2pb9NRP0RaZyYu0APl_UvHIcp0qJp_8Q276KXhuwxZQ6CwDVTL0-ABN645qO_C8MOzsn1Ey8PQAYKywbQL6ysW_XJqXsiznDl7suWvX0u42D9LO1rIbOzvIzg6ys7XsjbXs1r67WM279DcadMeu</recordid><startdate>201101</startdate><enddate>201101</enddate><creator>Shin, Min Kyoo</creator><creator>Kim, Hong Gi</creator><creator>Kim, Kil Lyong</creator><general>Blackwell Publishing Ltd</general><general>Wiley-Blackwell</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QR</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>201101</creationdate><title>A novel trimeric peptide, Neuropep‐1‐stimulating brain‐derived neurotrophic factor expression in rat brain improves spatial learning and memory as measured by the Y‐maze and Morris water maze</title><author>Shin, Min Kyoo ; Kim, Hong Gi ; Kim, Kil Lyong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4088-ae67ec8627e4411a63c76f115265c9f0f6dfa916e4422101ed2a2e67914666013</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adult and adolescent clinical studies</topic><topic>AKT protein</topic><topic>Alzheimer's disease</topic><topic>Animals</topic><topic>Anxiety</topic><topic>Biological and medical sciences</topic><topic>Brain Chemistry - physiology</topic><topic>Brain-derived neurotrophic factor</topic><topic>Brain-Derived Neurotrophic Factor - administration & dosage</topic><topic>Brain-Derived Neurotrophic Factor - biosynthesis</topic><topic>Brain-Derived Neurotrophic Factor - physiology</topic><topic>Cell Line</topic><topic>Combinatorial libraries</topic><topic>cortex</topic><topic>Cyclic AMP</topic><topic>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</topic><topic>Depression</topic><topic>Extracellular signal-regulated kinase</topic><topic>Hippocampus</topic><topic>Hippocampus - metabolism</topic><topic>Hippocampus - physiology</topic><topic>Learning</topic><topic>Male</topic><topic>Maze Learning - physiology</topic><topic>Medical sciences</topic><topic>Memory</topic><topic>Memory - physiology</topic><topic>Movement disorders</topic><topic>mRNA</topic><topic>Neurochemistry</topic><topic>Neurodegenerative diseases</topic><topic>Neurological diseases</topic><topic>Neurology</topic><topic>Neuromodulation</topic><topic>Neuropeptides - administration & dosage</topic><topic>Neuropeptides - chemistry</topic><topic>Neuropeptides - physiology</topic><topic>Oligopeptides - chemistry</topic><topic>Oligopeptides - physiology</topic><topic>Organic mental disorders. Neuropsychology</topic><topic>Parkinson's disease</topic><topic>Peptide Library</topic><topic>Peptides</topic><topic>Phosphorylation</topic><topic>Protein Multimerization - physiology</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopathology. Psychiatry</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptor, trkB - metabolism</topic><topic>Receptor, trkB - physiology</topic><topic>Regulatory sequences</topic><topic>Rodents</topic><topic>Signal transduction</topic><topic>Signal Transduction - physiology</topic><topic>Spatial Behavior - physiology</topic><topic>Spatial discrimination learning</topic><topic>spatial memory</topic><topic>Stress</topic><topic>TrkB receptors</topic><topic>Veins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shin, Min Kyoo</creatorcontrib><creatorcontrib>Kim, Hong Gi</creatorcontrib><creatorcontrib>Kim, Kil Lyong</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of neurochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shin, Min Kyoo</au><au>Kim, Hong Gi</au><au>Kim, Kil Lyong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A novel trimeric peptide, Neuropep‐1‐stimulating brain‐derived neurotrophic factor expression in rat brain improves spatial learning and memory as measured by the Y‐maze and Morris water maze</atitle><jtitle>Journal of neurochemistry</jtitle><addtitle>J Neurochem</addtitle><date>2011-01</date><risdate>2011</risdate><volume>116</volume><issue>2</issue><spage>205</spage><epage>216</epage><pages>205-216</pages><issn>0022-3042</issn><eissn>1471-4159</eissn><coden>JONRA9</coden><abstract>J. Neurochem. (2011) 116, 205–216.
Abundant studies have shown possible links between low levels of brain‐derived neurotrophic factor (BDNF) and neurological diseases such as Alzheimer’s disease, Parkinson’s disease, and depression, as well as stress and anxiety; therefore, BDNF could be a therapeutic target for neurological disorders. In the present study, a positional scanning‐synthetic peptide combinatorial library was utilized to identify a peptide modulator of BDNF expression in the hippocampal neuronal cell line, H19‐7. A novel tripeptide (Neuropep‐1) induced a significant increase of BDNF mRNA and protein levels in H19‐7 cells. Pre‐treatment of TrkB inhibitor (K252a) did not block Neuropep‐1‐induced BDNF up‐regulation. These results indicate that Neuropep‐1 may up‐regulate BDNF expression that might be independent of the TrkB receptor pathway. Tail vein injection of Neuropep‐1 significantly up‐regulated BDNF expression, TrkB phosphorylation, and its downstream signals including activation of Akt, ERK, and cAMP response element binding in the rat hippocampus. To evaluate improvement of spatial learning and memory (SLM) by Neuropep‐1‐induced BDNF up‐regulation, the Y‐maze and Morris water maze tests were performed. These results showed Neuropep‐1 injection improved SLM performance with increase of BDNF and TrkB expression, activation of TrkB downstream signals in rat hippocampus compared with the control group. However, phosphorylation levels of TrkB were not changed when it was normalized to the level of TrkB expression. The difference on TrkB phosphorylation in Neuropep‐1‐injected rats may be affected by behavioral tests. These results suggest that Neuropep‐1 may improve SLM via activation of the BDNF/TrkB signaling pathway in the rat hippocampus. Therefore, our findings represent that Neuropep‐1 might be a potential candidate for treatment of learning and memory disorders as well as neurological diseases involving the abnormal expression of BDNF.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>21044076</pmid><doi>10.1111/j.1471-4159.2010.07078.x</doi><tpages>12</tpages></addata></record> |
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subjects | Adult and adolescent clinical studies AKT protein Alzheimer's disease Animals Anxiety Biological and medical sciences Brain Chemistry - physiology Brain-derived neurotrophic factor Brain-Derived Neurotrophic Factor - administration & dosage Brain-Derived Neurotrophic Factor - biosynthesis Brain-Derived Neurotrophic Factor - physiology Cell Line Combinatorial libraries cortex Cyclic AMP Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Depression Extracellular signal-regulated kinase Hippocampus Hippocampus - metabolism Hippocampus - physiology Learning Male Maze Learning - physiology Medical sciences Memory Memory - physiology Movement disorders mRNA Neurochemistry Neurodegenerative diseases Neurological diseases Neurology Neuromodulation Neuropeptides - administration & dosage Neuropeptides - chemistry Neuropeptides - physiology Oligopeptides - chemistry Oligopeptides - physiology Organic mental disorders. Neuropsychology Parkinson's disease Peptide Library Peptides Phosphorylation Protein Multimerization - physiology Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Rats Rats, Sprague-Dawley Receptor, trkB - metabolism Receptor, trkB - physiology Regulatory sequences Rodents Signal transduction Signal Transduction - physiology Spatial Behavior - physiology Spatial discrimination learning spatial memory Stress TrkB receptors Veins |
title | A novel trimeric peptide, Neuropep‐1‐stimulating brain‐derived neurotrophic factor expression in rat brain improves spatial learning and memory as measured by the Y‐maze and Morris water maze |
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