Rutin Alleviates Prion Peptide-Induced Cell Death Through Inhibiting Apoptotic Pathway Activation in Dopaminergic Neuronal Cells

Prion disorders are progressive neurodegenerative diseases characterized by extensive neuronal loss and accumulation of the abnormal form of the scrapie prion protein (PrP). Rutin is a flavonoid that occurs naturally in plant-derived beverages and foods and is used in traditional and folkloric medic...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Cellular and molecular neurobiology 2014-10, Vol.34 (7), p.1071-1079
Hauptverfasser: Na, Ji-Young, Kim, Sokho, Song, Kibbeum, Kwon, Jungkee
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1079
container_issue 7
container_start_page 1071
container_title Cellular and molecular neurobiology
container_volume 34
creator Na, Ji-Young
Kim, Sokho
Song, Kibbeum
Kwon, Jungkee
description Prion disorders are progressive neurodegenerative diseases characterized by extensive neuronal loss and accumulation of the abnormal form of the scrapie prion protein (PrP). Rutin is a flavonoid that occurs naturally in plant-derived beverages and foods and is used in traditional and folkloric medicine worldwide. In the present study, we evaluated the protective effects of rutin against PrP fragment (106–126)-induced neuronal cell death. Rutin treatment blocked PrP(106–126)-mediated increases in reactive oxygen species production and nitric oxide release and helped slowing the decrease of neurotrophic factors that results from PrP accumulation. Rutin attenuated PrP(106–126)-associated mitochondrial apoptotic events by inhibiting mitochondrial permeability transition and caspase-3 activity and blocking expression of the apoptotic signals Bax and PARP. Additionally, rutin treatment significantly decreased the expression of the death receptor Fas and its ligand Fas-L. Overall, our results demonstrated that rutin protects against the neurodegenerative effects of prion accumulation by increasing production of neurotropic factors and inhibiting apoptotic pathway activation in neuronal cells. These results suggested that rutin may have clinical benefits for prion diseases and other neurodegenerative disorders.
doi_str_mv 10.1007/s10571-014-0084-3
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1561980344</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1561980344</sourcerecordid><originalsourceid>FETCH-LOGICAL-c344t-3da2665d64b3a1d47f4a455b76dfe3a3677c8878eae4a87dad92e5d91fa584923</originalsourceid><addsrcrecordid>eNp9kEFv0zAYhi3ExMrgB3BBPnLJ-BzbsXOsOmCVJlZN29ly4y-tpzQOtjO0Gz8dlw6OnHzw8z62HkI-MLhkAOpzYiAVq4CJCkCLir8iCyYVrxrN4TVZQK3qSnAB5-RtSo8A0ALIN-S8liC0hmZBft3N2Y90OQz45G3GRDfRh5FucMreYbUe3dyhoyscBnqFNu_p_T6Geben63Hvt76sd3Q5hSmH7Du6KcRP-0yXXfZPNh9VRX8VJnvwI8ZdQb7jHMNohz_O9I6c9XZI-P7lvCAPX7_cr66rm9tv69Xypuq4ELniztZNI10jttwyJ1QvrJByqxrXI7e8UarTWmm0KKxWzrq2Rula1lupRVvzC_Lp5J1i-DFjyubgU1d-YEcMczJMNqzVUB4rKDuhXQwpRezNFP3BxmfDwBzDm1N4U8KbY3jDy-bji37eHtD9W_wtXYD6BKRyNe4wmscwx5Ih_cf6Gzk_j5w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1561980344</pqid></control><display><type>article</type><title>Rutin Alleviates Prion Peptide-Induced Cell Death Through Inhibiting Apoptotic Pathway Activation in Dopaminergic Neuronal Cells</title><source>MEDLINE</source><source>SpringerNature Journals</source><creator>Na, Ji-Young ; Kim, Sokho ; Song, Kibbeum ; Kwon, Jungkee</creator><creatorcontrib>Na, Ji-Young ; Kim, Sokho ; Song, Kibbeum ; Kwon, Jungkee</creatorcontrib><description>Prion disorders are progressive neurodegenerative diseases characterized by extensive neuronal loss and accumulation of the abnormal form of the scrapie prion protein (PrP). Rutin is a flavonoid that occurs naturally in plant-derived beverages and foods and is used in traditional and folkloric medicine worldwide. In the present study, we evaluated the protective effects of rutin against PrP fragment (106–126)-induced neuronal cell death. Rutin treatment blocked PrP(106–126)-mediated increases in reactive oxygen species production and nitric oxide release and helped slowing the decrease of neurotrophic factors that results from PrP accumulation. Rutin attenuated PrP(106–126)-associated mitochondrial apoptotic events by inhibiting mitochondrial permeability transition and caspase-3 activity and blocking expression of the apoptotic signals Bax and PARP. Additionally, rutin treatment significantly decreased the expression of the death receptor Fas and its ligand Fas-L. Overall, our results demonstrated that rutin protects against the neurodegenerative effects of prion accumulation by increasing production of neurotropic factors and inhibiting apoptotic pathway activation in neuronal cells. These results suggested that rutin may have clinical benefits for prion diseases and other neurodegenerative disorders.</description><identifier>ISSN: 0272-4340</identifier><identifier>ISSN: 1573-6830</identifier><identifier>EISSN: 1573-6830</identifier><identifier>DOI: 10.1007/s10571-014-0084-3</identifier><identifier>PMID: 25048806</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Amino Acid Sequence ; Animals ; Apoptosis - drug effects ; Biomedical and Life Sciences ; Biomedicine ; Caspase 3 - metabolism ; Caspase 8 - metabolism ; Cell Biology ; Cell Line ; Dopaminergic Neurons - drug effects ; Dopaminergic Neurons - enzymology ; Dopaminergic Neurons - pathology ; Fas Ligand Protein - metabolism ; fas Receptor - metabolism ; Mice ; Mitochondrial Membrane Transport Proteins - metabolism ; Mitochondrial Permeability Transition Pore ; Mitochondrial Proteins - metabolism ; Molecular Sequence Data ; Nerve Growth Factors - metabolism ; Neurobiology ; Neuroprotective Agents - pharmacology ; Neurosciences ; Nitric Oxide - biosynthesis ; Original Research ; Peptide Fragments - chemistry ; Peptide Fragments - toxicity ; Prions - chemistry ; Prions - toxicity ; Reactive Oxygen Species - metabolism ; Rutin - pharmacology ; Signal Transduction - drug effects</subject><ispartof>Cellular and molecular neurobiology, 2014-10, Vol.34 (7), p.1071-1079</ispartof><rights>Springer Science+Business Media New York 2014</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c344t-3da2665d64b3a1d47f4a455b76dfe3a3677c8878eae4a87dad92e5d91fa584923</citedby><cites>FETCH-LOGICAL-c344t-3da2665d64b3a1d47f4a455b76dfe3a3677c8878eae4a87dad92e5d91fa584923</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10571-014-0084-3$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10571-014-0084-3$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25048806$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Na, Ji-Young</creatorcontrib><creatorcontrib>Kim, Sokho</creatorcontrib><creatorcontrib>Song, Kibbeum</creatorcontrib><creatorcontrib>Kwon, Jungkee</creatorcontrib><title>Rutin Alleviates Prion Peptide-Induced Cell Death Through Inhibiting Apoptotic Pathway Activation in Dopaminergic Neuronal Cells</title><title>Cellular and molecular neurobiology</title><addtitle>Cell Mol Neurobiol</addtitle><addtitle>Cell Mol Neurobiol</addtitle><description>Prion disorders are progressive neurodegenerative diseases characterized by extensive neuronal loss and accumulation of the abnormal form of the scrapie prion protein (PrP). Rutin is a flavonoid that occurs naturally in plant-derived beverages and foods and is used in traditional and folkloric medicine worldwide. In the present study, we evaluated the protective effects of rutin against PrP fragment (106–126)-induced neuronal cell death. Rutin treatment blocked PrP(106–126)-mediated increases in reactive oxygen species production and nitric oxide release and helped slowing the decrease of neurotrophic factors that results from PrP accumulation. Rutin attenuated PrP(106–126)-associated mitochondrial apoptotic events by inhibiting mitochondrial permeability transition and caspase-3 activity and blocking expression of the apoptotic signals Bax and PARP. Additionally, rutin treatment significantly decreased the expression of the death receptor Fas and its ligand Fas-L. Overall, our results demonstrated that rutin protects against the neurodegenerative effects of prion accumulation by increasing production of neurotropic factors and inhibiting apoptotic pathway activation in neuronal cells. These results suggested that rutin may have clinical benefits for prion diseases and other neurodegenerative disorders.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Apoptosis - drug effects</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Caspase 3 - metabolism</subject><subject>Caspase 8 - metabolism</subject><subject>Cell Biology</subject><subject>Cell Line</subject><subject>Dopaminergic Neurons - drug effects</subject><subject>Dopaminergic Neurons - enzymology</subject><subject>Dopaminergic Neurons - pathology</subject><subject>Fas Ligand Protein - metabolism</subject><subject>fas Receptor - metabolism</subject><subject>Mice</subject><subject>Mitochondrial Membrane Transport Proteins - metabolism</subject><subject>Mitochondrial Permeability Transition Pore</subject><subject>Mitochondrial Proteins - metabolism</subject><subject>Molecular Sequence Data</subject><subject>Nerve Growth Factors - metabolism</subject><subject>Neurobiology</subject><subject>Neuroprotective Agents - pharmacology</subject><subject>Neurosciences</subject><subject>Nitric Oxide - biosynthesis</subject><subject>Original Research</subject><subject>Peptide Fragments - chemistry</subject><subject>Peptide Fragments - toxicity</subject><subject>Prions - chemistry</subject><subject>Prions - toxicity</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>Rutin - pharmacology</subject><subject>Signal Transduction - drug effects</subject><issn>0272-4340</issn><issn>1573-6830</issn><issn>1573-6830</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEFv0zAYhi3ExMrgB3BBPnLJ-BzbsXOsOmCVJlZN29ly4y-tpzQOtjO0Gz8dlw6OnHzw8z62HkI-MLhkAOpzYiAVq4CJCkCLir8iCyYVrxrN4TVZQK3qSnAB5-RtSo8A0ALIN-S8liC0hmZBft3N2Y90OQz45G3GRDfRh5FucMreYbUe3dyhoyscBnqFNu_p_T6Geben63Hvt76sd3Q5hSmH7Du6KcRP-0yXXfZPNh9VRX8VJnvwI8ZdQb7jHMNohz_O9I6c9XZI-P7lvCAPX7_cr66rm9tv69Xypuq4ELniztZNI10jttwyJ1QvrJByqxrXI7e8UarTWmm0KKxWzrq2Rula1lupRVvzC_Lp5J1i-DFjyubgU1d-YEcMczJMNqzVUB4rKDuhXQwpRezNFP3BxmfDwBzDm1N4U8KbY3jDy-bji37eHtD9W_wtXYD6BKRyNe4wmscwx5Ih_cf6Gzk_j5w</recordid><startdate>20141001</startdate><enddate>20141001</enddate><creator>Na, Ji-Young</creator><creator>Kim, Sokho</creator><creator>Song, Kibbeum</creator><creator>Kwon, Jungkee</creator><general>Springer US</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>7X8</scope></search><sort><creationdate>20141001</creationdate><title>Rutin Alleviates Prion Peptide-Induced Cell Death Through Inhibiting Apoptotic Pathway Activation in Dopaminergic Neuronal Cells</title><author>Na, Ji-Young ; Kim, Sokho ; Song, Kibbeum ; Kwon, Jungkee</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c344t-3da2665d64b3a1d47f4a455b76dfe3a3677c8878eae4a87dad92e5d91fa584923</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Apoptosis - drug effects</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Caspase 3 - metabolism</topic><topic>Caspase 8 - metabolism</topic><topic>Cell Biology</topic><topic>Cell Line</topic><topic>Dopaminergic Neurons - drug effects</topic><topic>Dopaminergic Neurons - enzymology</topic><topic>Dopaminergic Neurons - pathology</topic><topic>Fas Ligand Protein - metabolism</topic><topic>fas Receptor - metabolism</topic><topic>Mice</topic><topic>Mitochondrial Membrane Transport Proteins - metabolism</topic><topic>Mitochondrial Permeability Transition Pore</topic><topic>Mitochondrial Proteins - metabolism</topic><topic>Molecular Sequence Data</topic><topic>Nerve Growth Factors - metabolism</topic><topic>Neurobiology</topic><topic>Neuroprotective Agents - pharmacology</topic><topic>Neurosciences</topic><topic>Nitric Oxide - biosynthesis</topic><topic>Original Research</topic><topic>Peptide Fragments - chemistry</topic><topic>Peptide Fragments - toxicity</topic><topic>Prions - chemistry</topic><topic>Prions - toxicity</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>Rutin - pharmacology</topic><topic>Signal Transduction - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Na, Ji-Young</creatorcontrib><creatorcontrib>Kim, Sokho</creatorcontrib><creatorcontrib>Song, Kibbeum</creatorcontrib><creatorcontrib>Kwon, Jungkee</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Cellular and molecular neurobiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Na, Ji-Young</au><au>Kim, Sokho</au><au>Song, Kibbeum</au><au>Kwon, Jungkee</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rutin Alleviates Prion Peptide-Induced Cell Death Through Inhibiting Apoptotic Pathway Activation in Dopaminergic Neuronal Cells</atitle><jtitle>Cellular and molecular neurobiology</jtitle><stitle>Cell Mol Neurobiol</stitle><addtitle>Cell Mol Neurobiol</addtitle><date>2014-10-01</date><risdate>2014</risdate><volume>34</volume><issue>7</issue><spage>1071</spage><epage>1079</epage><pages>1071-1079</pages><issn>0272-4340</issn><issn>1573-6830</issn><eissn>1573-6830</eissn><abstract>Prion disorders are progressive neurodegenerative diseases characterized by extensive neuronal loss and accumulation of the abnormal form of the scrapie prion protein (PrP). Rutin is a flavonoid that occurs naturally in plant-derived beverages and foods and is used in traditional and folkloric medicine worldwide. In the present study, we evaluated the protective effects of rutin against PrP fragment (106–126)-induced neuronal cell death. Rutin treatment blocked PrP(106–126)-mediated increases in reactive oxygen species production and nitric oxide release and helped slowing the decrease of neurotrophic factors that results from PrP accumulation. Rutin attenuated PrP(106–126)-associated mitochondrial apoptotic events by inhibiting mitochondrial permeability transition and caspase-3 activity and blocking expression of the apoptotic signals Bax and PARP. Additionally, rutin treatment significantly decreased the expression of the death receptor Fas and its ligand Fas-L. Overall, our results demonstrated that rutin protects against the neurodegenerative effects of prion accumulation by increasing production of neurotropic factors and inhibiting apoptotic pathway activation in neuronal cells. These results suggested that rutin may have clinical benefits for prion diseases and other neurodegenerative disorders.</abstract><cop>Boston</cop><pub>Springer US</pub><pmid>25048806</pmid><doi>10.1007/s10571-014-0084-3</doi><tpages>9</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0272-4340
ispartof Cellular and molecular neurobiology, 2014-10, Vol.34 (7), p.1071-1079
issn 0272-4340
1573-6830
1573-6830
language eng
recordid cdi_proquest_miscellaneous_1561980344
source MEDLINE; SpringerNature Journals
subjects Amino Acid Sequence
Animals
Apoptosis - drug effects
Biomedical and Life Sciences
Biomedicine
Caspase 3 - metabolism
Caspase 8 - metabolism
Cell Biology
Cell Line
Dopaminergic Neurons - drug effects
Dopaminergic Neurons - enzymology
Dopaminergic Neurons - pathology
Fas Ligand Protein - metabolism
fas Receptor - metabolism
Mice
Mitochondrial Membrane Transport Proteins - metabolism
Mitochondrial Permeability Transition Pore
Mitochondrial Proteins - metabolism
Molecular Sequence Data
Nerve Growth Factors - metabolism
Neurobiology
Neuroprotective Agents - pharmacology
Neurosciences
Nitric Oxide - biosynthesis
Original Research
Peptide Fragments - chemistry
Peptide Fragments - toxicity
Prions - chemistry
Prions - toxicity
Reactive Oxygen Species - metabolism
Rutin - pharmacology
Signal Transduction - drug effects
title Rutin Alleviates Prion Peptide-Induced Cell Death Through Inhibiting Apoptotic Pathway Activation in Dopaminergic Neuronal Cells
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T16%3A36%3A22IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Rutin%20Alleviates%20Prion%20Peptide-Induced%20Cell%20Death%20Through%20Inhibiting%20Apoptotic%20Pathway%20Activation%20in%20Dopaminergic%20Neuronal%20Cells&rft.jtitle=Cellular%20and%20molecular%20neurobiology&rft.au=Na,%20Ji-Young&rft.date=2014-10-01&rft.volume=34&rft.issue=7&rft.spage=1071&rft.epage=1079&rft.pages=1071-1079&rft.issn=0272-4340&rft.eissn=1573-6830&rft_id=info:doi/10.1007/s10571-014-0084-3&rft_dat=%3Cproquest_cross%3E1561980344%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1561980344&rft_id=info:pmid/25048806&rfr_iscdi=true