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...
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Veröffentlicht in: | Cellular and molecular neurobiology 2014-10, Vol.34 (7), p.1071-1079 |
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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 |
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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> |
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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 |
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