Gender differences in glutathione metabolism in Alzheimer's disease
The mechanism underlying Alzheimer's disease (AD), an age‐related neurodegenerative disease, is still an area of significant controversy. Oxidative damage of macromolecules has been suggested to play an important role in the development of AD; however, the underlying mechanism is still unclear....
Gespeichert in:
Veröffentlicht in: | Journal of neuroscience research 2005-03, Vol.79 (6), p.861-867 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 867 |
---|---|
container_issue | 6 |
container_start_page | 861 |
container_title | Journal of neuroscience research |
container_volume | 79 |
creator | Liu, Honglei Harrell, Lindy E. Shenvi, Swapna Hagen, Tory Liu, Rui-Ming |
description | The mechanism underlying Alzheimer's disease (AD), an age‐related neurodegenerative disease, is still an area of significant controversy. Oxidative damage of macromolecules has been suggested to play an important role in the development of AD; however, the underlying mechanism is still unclear. In this study, we showed that the concentration of glutathione (GSH), the most abundant intracellular free thiol and an important antioxidant, was decreased in red blood cells from male AD patients compared with age‐ and gender‐matched controls. However, there was no difference in blood GSH concentration between the female patients and female controls. The decrease in GSH content in red blood cells from male AD patients was associated with reduced activities of glutamate cysteine ligase and glutathione synthase, the two enzymes involved in de novo GSH synthesis, with no change in the amount of oxidized glutathione or the activity of glutathione reductase, suggesting that a decreased de novo GSH synthetic capacity is responsible for the decline in GSH content in AD. These results showed for the first time that GSH metabolism was regulated differently in male and female AD patients. © 2005 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/jnr.20424 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_67451033</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>67451033</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3614-260697960725a30d17f2f698f2b0dfa2f7010245fed07ef2a2ce471abb6cad8f3</originalsourceid><addsrcrecordid>eNp1kEtLAzEURoMoWh8L_4B0pbiYevOYxCylaFWKig8ENyEzc6PRedRkio9f79RWXbnK4p7vEA4h2xQGFIAdPNdhwEAwsUR6FLRKRCrUMukBl5AIoGyNrMf4DABap3yVrNFUag6M9chwhHWBoV945zBgnWPs-7r_WE5b2z75psZ-ha3NmtLHanY5Kj-f0FcY9mI3imgjbpIVZ8uIW4t3g9ydHN8OT5Px5ehseDROci6pSJgEqZWWoFhqORRUOeakPnQsg8JZ5hRQYCJ1WIBCxyzLUShqs0zmtjh0fIPszr2T0LxOMbam8jHHsrQ1NtNopBIpBc47cH8O5qGJMaAzk-ArGz4MBTMrZrpi5rtYx-4spNOswuKPXCTqgIM58OZL_PjfZM4vrn-UyXzhY4vvvwsbXrovcpWa-4uRuWF6nOrbK_PAvwC3v4Pu</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>67451033</pqid></control><display><type>article</type><title>Gender differences in glutathione metabolism in Alzheimer's disease</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Liu, Honglei ; Harrell, Lindy E. ; Shenvi, Swapna ; Hagen, Tory ; Liu, Rui-Ming</creator><creatorcontrib>Liu, Honglei ; Harrell, Lindy E. ; Shenvi, Swapna ; Hagen, Tory ; Liu, Rui-Ming</creatorcontrib><description>The mechanism underlying Alzheimer's disease (AD), an age‐related neurodegenerative disease, is still an area of significant controversy. Oxidative damage of macromolecules has been suggested to play an important role in the development of AD; however, the underlying mechanism is still unclear. In this study, we showed that the concentration of glutathione (GSH), the most abundant intracellular free thiol and an important antioxidant, was decreased in red blood cells from male AD patients compared with age‐ and gender‐matched controls. However, there was no difference in blood GSH concentration between the female patients and female controls. The decrease in GSH content in red blood cells from male AD patients was associated with reduced activities of glutamate cysteine ligase and glutathione synthase, the two enzymes involved in de novo GSH synthesis, with no change in the amount of oxidized glutathione or the activity of glutathione reductase, suggesting that a decreased de novo GSH synthetic capacity is responsible for the decline in GSH content in AD. These results showed for the first time that GSH metabolism was regulated differently in male and female AD patients. © 2005 Wiley‐Liss, Inc.</description><identifier>ISSN: 0360-4012</identifier><identifier>EISSN: 1097-4547</identifier><identifier>DOI: 10.1002/jnr.20424</identifier><identifier>PMID: 15693022</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Aged ; Alzheimer Disease - metabolism ; Alzheimer's disease ; Analysis of Variance ; Case-Control Studies ; Chromatography, High Pressure Liquid - methods ; Electrochemistry - methods ; Erythrocytes - metabolism ; gender ; Glutamate-Cysteine Ligase - blood ; glutathione ; Glutathione - metabolism ; Glutathione Disulfide - blood ; Glutathione Synthase - blood ; Humans ; Leukocytes - metabolism ; Male ; Mental Status Schedule ; Sex Characteristics</subject><ispartof>Journal of neuroscience research, 2005-03, Vol.79 (6), p.861-867</ispartof><rights>Copyright © 2005 Wiley‐Liss, Inc.</rights><rights>Copyright 2005 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3614-260697960725a30d17f2f698f2b0dfa2f7010245fed07ef2a2ce471abb6cad8f3</citedby><cites>FETCH-LOGICAL-c3614-260697960725a30d17f2f698f2b0dfa2f7010245fed07ef2a2ce471abb6cad8f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjnr.20424$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjnr.20424$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15693022$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Honglei</creatorcontrib><creatorcontrib>Harrell, Lindy E.</creatorcontrib><creatorcontrib>Shenvi, Swapna</creatorcontrib><creatorcontrib>Hagen, Tory</creatorcontrib><creatorcontrib>Liu, Rui-Ming</creatorcontrib><title>Gender differences in glutathione metabolism in Alzheimer's disease</title><title>Journal of neuroscience research</title><addtitle>J. Neurosci. Res</addtitle><description>The mechanism underlying Alzheimer's disease (AD), an age‐related neurodegenerative disease, is still an area of significant controversy. Oxidative damage of macromolecules has been suggested to play an important role in the development of AD; however, the underlying mechanism is still unclear. In this study, we showed that the concentration of glutathione (GSH), the most abundant intracellular free thiol and an important antioxidant, was decreased in red blood cells from male AD patients compared with age‐ and gender‐matched controls. However, there was no difference in blood GSH concentration between the female patients and female controls. The decrease in GSH content in red blood cells from male AD patients was associated with reduced activities of glutamate cysteine ligase and glutathione synthase, the two enzymes involved in de novo GSH synthesis, with no change in the amount of oxidized glutathione or the activity of glutathione reductase, suggesting that a decreased de novo GSH synthetic capacity is responsible for the decline in GSH content in AD. These results showed for the first time that GSH metabolism was regulated differently in male and female AD patients. © 2005 Wiley‐Liss, Inc.</description><subject>Aged</subject><subject>Alzheimer Disease - metabolism</subject><subject>Alzheimer's disease</subject><subject>Analysis of Variance</subject><subject>Case-Control Studies</subject><subject>Chromatography, High Pressure Liquid - methods</subject><subject>Electrochemistry - methods</subject><subject>Erythrocytes - metabolism</subject><subject>gender</subject><subject>Glutamate-Cysteine Ligase - blood</subject><subject>glutathione</subject><subject>Glutathione - metabolism</subject><subject>Glutathione Disulfide - blood</subject><subject>Glutathione Synthase - blood</subject><subject>Humans</subject><subject>Leukocytes - metabolism</subject><subject>Male</subject><subject>Mental Status Schedule</subject><subject>Sex Characteristics</subject><issn>0360-4012</issn><issn>1097-4547</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kEtLAzEURoMoWh8L_4B0pbiYevOYxCylaFWKig8ENyEzc6PRedRkio9f79RWXbnK4p7vEA4h2xQGFIAdPNdhwEAwsUR6FLRKRCrUMukBl5AIoGyNrMf4DABap3yVrNFUag6M9chwhHWBoV945zBgnWPs-7r_WE5b2z75psZ-ha3NmtLHanY5Kj-f0FcY9mI3imgjbpIVZ8uIW4t3g9ydHN8OT5Px5ehseDROci6pSJgEqZWWoFhqORRUOeakPnQsg8JZ5hRQYCJ1WIBCxyzLUShqs0zmtjh0fIPszr2T0LxOMbam8jHHsrQ1NtNopBIpBc47cH8O5qGJMaAzk-ArGz4MBTMrZrpi5rtYx-4spNOswuKPXCTqgIM58OZL_PjfZM4vrn-UyXzhY4vvvwsbXrovcpWa-4uRuWF6nOrbK_PAvwC3v4Pu</recordid><startdate>20050315</startdate><enddate>20050315</enddate><creator>Liu, Honglei</creator><creator>Harrell, Lindy E.</creator><creator>Shenvi, Swapna</creator><creator>Hagen, Tory</creator><creator>Liu, Rui-Ming</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</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></search><sort><creationdate>20050315</creationdate><title>Gender differences in glutathione metabolism in Alzheimer's disease</title><author>Liu, Honglei ; Harrell, Lindy E. ; Shenvi, Swapna ; Hagen, Tory ; Liu, Rui-Ming</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3614-260697960725a30d17f2f698f2b0dfa2f7010245fed07ef2a2ce471abb6cad8f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Aged</topic><topic>Alzheimer Disease - metabolism</topic><topic>Alzheimer's disease</topic><topic>Analysis of Variance</topic><topic>Case-Control Studies</topic><topic>Chromatography, High Pressure Liquid - methods</topic><topic>Electrochemistry - methods</topic><topic>Erythrocytes - metabolism</topic><topic>gender</topic><topic>Glutamate-Cysteine Ligase - blood</topic><topic>glutathione</topic><topic>Glutathione - metabolism</topic><topic>Glutathione Disulfide - blood</topic><topic>Glutathione Synthase - blood</topic><topic>Humans</topic><topic>Leukocytes - metabolism</topic><topic>Male</topic><topic>Mental Status Schedule</topic><topic>Sex Characteristics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Honglei</creatorcontrib><creatorcontrib>Harrell, Lindy E.</creatorcontrib><creatorcontrib>Shenvi, Swapna</creatorcontrib><creatorcontrib>Hagen, Tory</creatorcontrib><creatorcontrib>Liu, Rui-Ming</creatorcontrib><collection>Istex</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><jtitle>Journal of neuroscience research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Honglei</au><au>Harrell, Lindy E.</au><au>Shenvi, Swapna</au><au>Hagen, Tory</au><au>Liu, Rui-Ming</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Gender differences in glutathione metabolism in Alzheimer's disease</atitle><jtitle>Journal of neuroscience research</jtitle><addtitle>J. Neurosci. Res</addtitle><date>2005-03-15</date><risdate>2005</risdate><volume>79</volume><issue>6</issue><spage>861</spage><epage>867</epage><pages>861-867</pages><issn>0360-4012</issn><eissn>1097-4547</eissn><abstract>The mechanism underlying Alzheimer's disease (AD), an age‐related neurodegenerative disease, is still an area of significant controversy. Oxidative damage of macromolecules has been suggested to play an important role in the development of AD; however, the underlying mechanism is still unclear. In this study, we showed that the concentration of glutathione (GSH), the most abundant intracellular free thiol and an important antioxidant, was decreased in red blood cells from male AD patients compared with age‐ and gender‐matched controls. However, there was no difference in blood GSH concentration between the female patients and female controls. The decrease in GSH content in red blood cells from male AD patients was associated with reduced activities of glutamate cysteine ligase and glutathione synthase, the two enzymes involved in de novo GSH synthesis, with no change in the amount of oxidized glutathione or the activity of glutathione reductase, suggesting that a decreased de novo GSH synthetic capacity is responsible for the decline in GSH content in AD. These results showed for the first time that GSH metabolism was regulated differently in male and female AD patients. © 2005 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>15693022</pmid><doi>10.1002/jnr.20424</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0360-4012 |
ispartof | Journal of neuroscience research, 2005-03, Vol.79 (6), p.861-867 |
issn | 0360-4012 1097-4547 |
language | eng |
recordid | cdi_proquest_miscellaneous_67451033 |
source | MEDLINE; Wiley Online Library Journals Frontfile Complete |
subjects | Aged Alzheimer Disease - metabolism Alzheimer's disease Analysis of Variance Case-Control Studies Chromatography, High Pressure Liquid - methods Electrochemistry - methods Erythrocytes - metabolism gender Glutamate-Cysteine Ligase - blood glutathione Glutathione - metabolism Glutathione Disulfide - blood Glutathione Synthase - blood Humans Leukocytes - metabolism Male Mental Status Schedule Sex Characteristics |
title | Gender differences in glutathione metabolism in Alzheimer's disease |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-09T18%3A31%3A14IST&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=Gender%20differences%20in%20glutathione%20metabolism%20in%20Alzheimer's%20disease&rft.jtitle=Journal%20of%20neuroscience%20research&rft.au=Liu,%20Honglei&rft.date=2005-03-15&rft.volume=79&rft.issue=6&rft.spage=861&rft.epage=867&rft.pages=861-867&rft.issn=0360-4012&rft.eissn=1097-4547&rft_id=info:doi/10.1002/jnr.20424&rft_dat=%3Cproquest_cross%3E67451033%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=67451033&rft_id=info:pmid/15693022&rfr_iscdi=true |