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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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Published in:Journal of neurochemistry 2011-01, Vol.116 (2), p.205-216
Main Authors: Shin, Min Kyoo, Kim, Hong Gi, Kim, Kil Lyong
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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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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><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 &amp; 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 &amp; 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&amp;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 &amp; 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 &amp; 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 &amp; 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 &amp; dosage</topic><topic>Neuropeptides - chemistry</topic><topic>Neuropeptides - physiology</topic><topic>Oligopeptides - chemistry</topic><topic>Oligopeptides - physiology</topic><topic>Organic mental disorders. 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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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source Wiley-Blackwell Read & Publish Collection; Free Full-Text Journals in Chemistry
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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