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Glutathione metabolism and Parkinson's disease
It has been established that oxidative stress, defined as the condition in which the sum of free radicals in a cell exceeds the antioxidant capacity of the cell, contributes to the pathogenesis of Parkinson disease. Glutathione is a ubiquitous thiol tripeptide that acts alone or in concert with enzy...
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Published in: | Free radical biology & medicine 2013-09, Vol.62, p.13-25 |
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description | It has been established that oxidative stress, defined as the condition in which the sum of free radicals in a cell exceeds the antioxidant capacity of the cell, contributes to the pathogenesis of Parkinson disease. Glutathione is a ubiquitous thiol tripeptide that acts alone or in concert with enzymes within cells to reduce superoxide radicals, hydroxyl radicals, and peroxynitrites. In this review, we examine the synthesis, metabolism, and functional interactions of glutathione and discuss how these relate to the protection of dopaminergic neurons from oxidative damage and its therapeutic potential in Parkinson disease.
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•Glutathione, a thiol tripeptide, is an important antioxidant in the brain.•GSH is critical for protecting DA neurons in the SNpc from free radical damage.•GPx and GSTs catalyze the reduction of electrophiles using GSH.•GST mutations combined with environmental insults correlate with increased PD risk.•Maintaining GSH levels may provide a therapeutic treatment for PD. |
doi_str_mv | 10.1016/j.freeradbiomed.2013.05.001 |
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[Display omitted]
•Glutathione, a thiol tripeptide, is an important antioxidant in the brain.•GSH is critical for protecting DA neurons in the SNpc from free radical damage.•GPx and GSTs catalyze the reduction of electrophiles using GSH.•GST mutations combined with environmental insults correlate with increased PD risk.•Maintaining GSH levels may provide a therapeutic treatment for PD.</description><identifier>ISSN: 0891-5849</identifier><identifier>EISSN: 1873-4596</identifier><identifier>DOI: 10.1016/j.freeradbiomed.2013.05.001</identifier><identifier>PMID: 23665395</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>antioxidant activity ; Antioxidants - metabolism ; Dopamine - metabolism ; Dopaminergic Neurons ; enzymes ; Glutathione ; Glutathione - metabolism ; Glutathione S-transferase ; Humans ; hydroxyl radicals ; metabolism ; Mitochondria - enzymology ; Mitochondria - metabolism ; neurons ; Oxidative Stress ; Parkinson disease ; Parkinson Disease - enzymology ; Parkinson Disease - metabolism ; Parkinson Disease - physiopathology ; Parkinson's disease ; pathogenesis ; Substantia nigra ; Substantia Nigra - enzymology ; superoxide anion ; thiols</subject><ispartof>Free radical biology & medicine, 2013-09, Vol.62, p.13-25</ispartof><rights>2013 Elsevier Inc.</rights><rights>Copyright © 2013 Elsevier Inc. All rights reserved.</rights><rights>2013 Elsevier Inc. All rights reserved. 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c614t-df23c4df8d6291bc5b0d172d067b0c5c560dad1d304abf31e44b5c21514990863</citedby><cites>FETCH-LOGICAL-c614t-df23c4df8d6291bc5b0d172d067b0c5c560dad1d304abf31e44b5c21514990863</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23665395$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Smeyne, Michelle</creatorcontrib><creatorcontrib>Smeyne, Richard Jay</creatorcontrib><title>Glutathione metabolism and Parkinson's disease</title><title>Free radical biology & medicine</title><addtitle>Free Radic Biol Med</addtitle><description>It has been established that oxidative stress, defined as the condition in which the sum of free radicals in a cell exceeds the antioxidant capacity of the cell, contributes to the pathogenesis of Parkinson disease. Glutathione is a ubiquitous thiol tripeptide that acts alone or in concert with enzymes within cells to reduce superoxide radicals, hydroxyl radicals, and peroxynitrites. In this review, we examine the synthesis, metabolism, and functional interactions of glutathione and discuss how these relate to the protection of dopaminergic neurons from oxidative damage and its therapeutic potential in Parkinson disease.
[Display omitted]
•Glutathione, a thiol tripeptide, is an important antioxidant in the brain.•GSH is critical for protecting DA neurons in the SNpc from free radical damage.•GPx and GSTs catalyze the reduction of electrophiles using GSH.•GST mutations combined with environmental insults correlate with increased PD risk.•Maintaining GSH levels may provide a therapeutic treatment for PD.</description><subject>antioxidant activity</subject><subject>Antioxidants - metabolism</subject><subject>Dopamine - metabolism</subject><subject>Dopaminergic Neurons</subject><subject>enzymes</subject><subject>Glutathione</subject><subject>Glutathione - metabolism</subject><subject>Glutathione S-transferase</subject><subject>Humans</subject><subject>hydroxyl radicals</subject><subject>metabolism</subject><subject>Mitochondria - enzymology</subject><subject>Mitochondria - metabolism</subject><subject>neurons</subject><subject>Oxidative Stress</subject><subject>Parkinson disease</subject><subject>Parkinson Disease - enzymology</subject><subject>Parkinson Disease - metabolism</subject><subject>Parkinson Disease - physiopathology</subject><subject>Parkinson's disease</subject><subject>pathogenesis</subject><subject>Substantia nigra</subject><subject>Substantia Nigra - enzymology</subject><subject>superoxide anion</subject><subject>thiols</subject><issn>0891-5849</issn><issn>1873-4596</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqNkV9LHDEUxYNUdGv7FexCH-zLjPdO_swMBUHEWkFQaH0OmeSOZjszscms0G_fLGtFnyoE8pDfOZyTw9hnhBIB1fGq7CNRNK7zYSRXVoC8BFkC4A5bYFPzQshWvWMLaFosZCPaffY-pRUACMmbPbZfcaUkb-WClRfDejbzvQ8TLUeaTRcGn8almdzyxsRffkphOkpL5xOZRB_Ybm-GRB-f7gN2--3859n34ur64vLs9KqwCsVcuL7iVri-capqsbOyA4d15UDVHVhppQJnHDoOwnQ9RxKik7ZCiaJtoVH8gJ1sfR_WXe5oaZqjGfRD9KOJf3QwXr9-mfy9vguPmtdc5ZMNvjwZxPB7TWnWo0-WhsFMFNZJo-SiqeqM_x8VmJMpISGjX7eojSGlSP1zIgS9GUev9Ktx9GYcDVLncbL68GWpZ-2_NTLwaQv0JmhzF33Stz-yg9yocyuRifMtQfnzHz1FnaynyZLzkeysXfBvivIXCx-xEg</recordid><startdate>20130901</startdate><enddate>20130901</enddate><creator>Smeyne, Michelle</creator><creator>Smeyne, Richard Jay</creator><general>Elsevier Inc</general><scope>FBQ</scope><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><scope>7TK</scope><scope>5PM</scope></search><sort><creationdate>20130901</creationdate><title>Glutathione metabolism and Parkinson's disease</title><author>Smeyne, Michelle ; Smeyne, Richard Jay</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c614t-df23c4df8d6291bc5b0d172d067b0c5c560dad1d304abf31e44b5c21514990863</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>antioxidant activity</topic><topic>Antioxidants - metabolism</topic><topic>Dopamine - metabolism</topic><topic>Dopaminergic Neurons</topic><topic>enzymes</topic><topic>Glutathione</topic><topic>Glutathione - metabolism</topic><topic>Glutathione S-transferase</topic><topic>Humans</topic><topic>hydroxyl radicals</topic><topic>metabolism</topic><topic>Mitochondria - enzymology</topic><topic>Mitochondria - metabolism</topic><topic>neurons</topic><topic>Oxidative Stress</topic><topic>Parkinson disease</topic><topic>Parkinson Disease - enzymology</topic><topic>Parkinson Disease - metabolism</topic><topic>Parkinson Disease - physiopathology</topic><topic>Parkinson's disease</topic><topic>pathogenesis</topic><topic>Substantia nigra</topic><topic>Substantia Nigra - enzymology</topic><topic>superoxide anion</topic><topic>thiols</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Smeyne, Michelle</creatorcontrib><creatorcontrib>Smeyne, Richard Jay</creatorcontrib><collection>AGRIS</collection><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><collection>Neurosciences Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Free radical biology & medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Smeyne, Michelle</au><au>Smeyne, Richard Jay</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Glutathione metabolism and Parkinson's disease</atitle><jtitle>Free radical biology & medicine</jtitle><addtitle>Free Radic Biol Med</addtitle><date>2013-09-01</date><risdate>2013</risdate><volume>62</volume><spage>13</spage><epage>25</epage><pages>13-25</pages><issn>0891-5849</issn><eissn>1873-4596</eissn><abstract>It has been established that oxidative stress, defined as the condition in which the sum of free radicals in a cell exceeds the antioxidant capacity of the cell, contributes to the pathogenesis of Parkinson disease. Glutathione is a ubiquitous thiol tripeptide that acts alone or in concert with enzymes within cells to reduce superoxide radicals, hydroxyl radicals, and peroxynitrites. In this review, we examine the synthesis, metabolism, and functional interactions of glutathione and discuss how these relate to the protection of dopaminergic neurons from oxidative damage and its therapeutic potential in Parkinson disease.
[Display omitted]
•Glutathione, a thiol tripeptide, is an important antioxidant in the brain.•GSH is critical for protecting DA neurons in the SNpc from free radical damage.•GPx and GSTs catalyze the reduction of electrophiles using GSH.•GST mutations combined with environmental insults correlate with increased PD risk.•Maintaining GSH levels may provide a therapeutic treatment for PD.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>23665395</pmid><doi>10.1016/j.freeradbiomed.2013.05.001</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | antioxidant activity Antioxidants - metabolism Dopamine - metabolism Dopaminergic Neurons enzymes Glutathione Glutathione - metabolism Glutathione S-transferase Humans hydroxyl radicals metabolism Mitochondria - enzymology Mitochondria - metabolism neurons Oxidative Stress Parkinson disease Parkinson Disease - enzymology Parkinson Disease - metabolism Parkinson Disease - physiopathology Parkinson's disease pathogenesis Substantia nigra Substantia Nigra - enzymology superoxide anion thiols |
title | Glutathione metabolism and Parkinson's disease |
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