Human septic myopathy: Induction of cyclooxygenase, heme oxygenase and activation of the ubiquitin proteolytic pathway
Skeletal muscle failure and wasting are manifestations of sepsis in humans that leads to serious and prolonged complications. The authors investigated the role of the major proinflammatory and antiinflammatory pathways, namely the inducible isoforms cyclooxygenase (COX-2) and heme oxygenase (HO-1),...
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Veröffentlicht in: | Anesthesiology (Philadelphia) 2004-09, Vol.101 (3), p.583-590 |
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creator | RABUEL, Christophe RENAUD, Estelle BREALEY, David RATAJCZAK, Philippe DAMY, Thibaut ALVES, Arnaud HABIB, Aïda SINGER, Mervyn PAYEN, Didier MEBAZAA, Alexandre |
description | Skeletal muscle failure and wasting are manifestations of sepsis in humans that leads to serious and prolonged complications. The authors investigated the role of the major proinflammatory and antiinflammatory pathways, namely the inducible isoforms cyclooxygenase (COX-2) and heme oxygenase (HO-1), and the ubiquitin proteolytic pathway in skeletal muscle of septic patients.
Protein expression was detected by Western blot techniques. Muscle biopsies were taken from two muscle groups, rectus abdominis and vastus lateralis, of septic and control patients.
The study showed an increase in COX-2 and HO-1 proteins expression and an activation of the proteolytic ubiquitin pathway with a parallel increase in free ubiquitin and ubiquitinated proteins in skeletal muscle of septic but not of control patients. In addition, those patients who would die from septic shock expressed more COX-2 and HO-1 proteins in muscle biopsies than did those patients who would survive.
This study showed a marked involvement of local proinflammatory and antiinflammatory pathways and, more importantly, demonstrated the existence of an active ubiquitin proteolytic pathway in skeletal muscle of septic patients. Activation of ubiquitin pathway could be involved in sepsis-related muscle catabolism and wasting. |
doi_str_mv | 10.1097/00000542-200409000-00006 |
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Protein expression was detected by Western blot techniques. Muscle biopsies were taken from two muscle groups, rectus abdominis and vastus lateralis, of septic and control patients.
The study showed an increase in COX-2 and HO-1 proteins expression and an activation of the proteolytic ubiquitin pathway with a parallel increase in free ubiquitin and ubiquitinated proteins in skeletal muscle of septic but not of control patients. In addition, those patients who would die from septic shock expressed more COX-2 and HO-1 proteins in muscle biopsies than did those patients who would survive.
This study showed a marked involvement of local proinflammatory and antiinflammatory pathways and, more importantly, demonstrated the existence of an active ubiquitin proteolytic pathway in skeletal muscle of septic patients. Activation of ubiquitin pathway could be involved in sepsis-related muscle catabolism and wasting.</description><identifier>ISSN: 0003-3022</identifier><identifier>EISSN: 1528-1175</identifier><identifier>DOI: 10.1097/00000542-200409000-00006</identifier><identifier>PMID: 15329582</identifier><identifier>CODEN: ANESAV</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Anesthesia ; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Biological and medical sciences ; Blotting, Western ; Cyclooxygenase 1 ; Cyclooxygenase 2 ; Endopeptidases - metabolism ; Enzyme Induction - physiology ; Female ; Heme Oxygenase (Decyclizing) - biosynthesis ; Humans ; Immunohistochemistry ; Isoenzymes - biosynthesis ; Isoenzymes - genetics ; Male ; Medical sciences ; Membrane Proteins ; Middle Aged ; Muscular Diseases - enzymology ; Muscular Diseases - etiology ; Muscular Diseases - metabolism ; Prostaglandin-Endoperoxide Synthases - biosynthesis ; Prostaglandin-Endoperoxide Synthases - genetics ; Sepsis - complications ; Sepsis - enzymology ; Sepsis - metabolism ; Ubiquitin - metabolism</subject><ispartof>Anesthesiology (Philadelphia), 2004-09, Vol.101 (3), p.583-590</ispartof><rights>2004 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c407t-a7e8bc6365a4354f44c794d394617ac1b4b6281f8f762f307d5e57a3ba2d1d263</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16082070$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15329582$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>RABUEL, Christophe</creatorcontrib><creatorcontrib>RENAUD, Estelle</creatorcontrib><creatorcontrib>BREALEY, David</creatorcontrib><creatorcontrib>RATAJCZAK, Philippe</creatorcontrib><creatorcontrib>DAMY, Thibaut</creatorcontrib><creatorcontrib>ALVES, Arnaud</creatorcontrib><creatorcontrib>HABIB, Aïda</creatorcontrib><creatorcontrib>SINGER, Mervyn</creatorcontrib><creatorcontrib>PAYEN, Didier</creatorcontrib><creatorcontrib>MEBAZAA, Alexandre</creatorcontrib><title>Human septic myopathy: Induction of cyclooxygenase, heme oxygenase and activation of the ubiquitin proteolytic pathway</title><title>Anesthesiology (Philadelphia)</title><addtitle>Anesthesiology</addtitle><description>Skeletal muscle failure and wasting are manifestations of sepsis in humans that leads to serious and prolonged complications. The authors investigated the role of the major proinflammatory and antiinflammatory pathways, namely the inducible isoforms cyclooxygenase (COX-2) and heme oxygenase (HO-1), and the ubiquitin proteolytic pathway in skeletal muscle of septic patients.
Protein expression was detected by Western blot techniques. Muscle biopsies were taken from two muscle groups, rectus abdominis and vastus lateralis, of septic and control patients.
The study showed an increase in COX-2 and HO-1 proteins expression and an activation of the proteolytic ubiquitin pathway with a parallel increase in free ubiquitin and ubiquitinated proteins in skeletal muscle of septic but not of control patients. In addition, those patients who would die from septic shock expressed more COX-2 and HO-1 proteins in muscle biopsies than did those patients who would survive.
This study showed a marked involvement of local proinflammatory and antiinflammatory pathways and, more importantly, demonstrated the existence of an active ubiquitin proteolytic pathway in skeletal muscle of septic patients. Activation of ubiquitin pathway could be involved in sepsis-related muscle catabolism and wasting.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Anesthesia</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Biological and medical sciences</subject><subject>Blotting, Western</subject><subject>Cyclooxygenase 1</subject><subject>Cyclooxygenase 2</subject><subject>Endopeptidases - metabolism</subject><subject>Enzyme Induction - physiology</subject><subject>Female</subject><subject>Heme Oxygenase (Decyclizing) - biosynthesis</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Isoenzymes - biosynthesis</subject><subject>Isoenzymes - genetics</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Membrane Proteins</subject><subject>Middle Aged</subject><subject>Muscular Diseases - enzymology</subject><subject>Muscular Diseases - etiology</subject><subject>Muscular Diseases - metabolism</subject><subject>Prostaglandin-Endoperoxide Synthases - biosynthesis</subject><subject>Prostaglandin-Endoperoxide Synthases - genetics</subject><subject>Sepsis - complications</subject><subject>Sepsis - enzymology</subject><subject>Sepsis - metabolism</subject><subject>Ubiquitin - metabolism</subject><issn>0003-3022</issn><issn>1528-1175</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkEtPwzAQhC0EglL4C8gXOBHw2w43VPGSKnGBc7RxHGqUxCVOgPx7EtqCL9aMvt1ZDUKYkitKUn1NpicFSxghgqSjSCZH7aEZlcwklGq5j2ajxRNOGDtCxzG-j1JLbg7REZWcpdKwGfp87GtocHTrzltcD2EN3Wq4wU9N0dvOhwaHEtvBViF8D2-ugegu8crVDv9pDE2BYYQ_YTfQrRzuc__R-843eN2GzoVqmBKm9V8wnKCDEqroTrf_HL3e370sHpPl88PT4naZWEF0l4B2JreKKwmCS1EKYXUqCp4KRTVYmotcMUNLU2rFSk50IZ3UwHNgBS2Y4nN0sdk73vDRu9hltY_WVRU0LvQxU8pQRYQZQbMBbRtibF2ZrVtfQztklGRT59mu8-yv819ryjjbZvR57Yr_wW3JI3C-BSBaqMoWGuvjP6eIYUQT_gNkI4tF</recordid><startdate>20040901</startdate><enddate>20040901</enddate><creator>RABUEL, Christophe</creator><creator>RENAUD, Estelle</creator><creator>BREALEY, David</creator><creator>RATAJCZAK, Philippe</creator><creator>DAMY, Thibaut</creator><creator>ALVES, Arnaud</creator><creator>HABIB, Aïda</creator><creator>SINGER, Mervyn</creator><creator>PAYEN, Didier</creator><creator>MEBAZAA, Alexandre</creator><general>Lippincott</general><scope>IQODW</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>20040901</creationdate><title>Human septic myopathy: Induction of cyclooxygenase, heme oxygenase and activation of the ubiquitin proteolytic pathway</title><author>RABUEL, Christophe ; RENAUD, Estelle ; BREALEY, David ; RATAJCZAK, Philippe ; DAMY, Thibaut ; ALVES, Arnaud ; HABIB, Aïda ; SINGER, Mervyn ; PAYEN, Didier ; MEBAZAA, Alexandre</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c407t-a7e8bc6365a4354f44c794d394617ac1b4b6281f8f762f307d5e57a3ba2d1d263</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Anesthesia</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Biological and medical sciences</topic><topic>Blotting, Western</topic><topic>Cyclooxygenase 1</topic><topic>Cyclooxygenase 2</topic><topic>Endopeptidases - metabolism</topic><topic>Enzyme Induction - physiology</topic><topic>Female</topic><topic>Heme Oxygenase (Decyclizing) - biosynthesis</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Isoenzymes - biosynthesis</topic><topic>Isoenzymes - genetics</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Membrane Proteins</topic><topic>Middle Aged</topic><topic>Muscular Diseases - enzymology</topic><topic>Muscular Diseases - etiology</topic><topic>Muscular Diseases - metabolism</topic><topic>Prostaglandin-Endoperoxide Synthases - biosynthesis</topic><topic>Prostaglandin-Endoperoxide Synthases - genetics</topic><topic>Sepsis - complications</topic><topic>Sepsis - enzymology</topic><topic>Sepsis - metabolism</topic><topic>Ubiquitin - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>RABUEL, Christophe</creatorcontrib><creatorcontrib>RENAUD, Estelle</creatorcontrib><creatorcontrib>BREALEY, David</creatorcontrib><creatorcontrib>RATAJCZAK, Philippe</creatorcontrib><creatorcontrib>DAMY, Thibaut</creatorcontrib><creatorcontrib>ALVES, Arnaud</creatorcontrib><creatorcontrib>HABIB, Aïda</creatorcontrib><creatorcontrib>SINGER, Mervyn</creatorcontrib><creatorcontrib>PAYEN, Didier</creatorcontrib><creatorcontrib>MEBAZAA, Alexandre</creatorcontrib><collection>Pascal-Francis</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>Anesthesiology (Philadelphia)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>RABUEL, Christophe</au><au>RENAUD, Estelle</au><au>BREALEY, David</au><au>RATAJCZAK, Philippe</au><au>DAMY, Thibaut</au><au>ALVES, Arnaud</au><au>HABIB, Aïda</au><au>SINGER, Mervyn</au><au>PAYEN, Didier</au><au>MEBAZAA, Alexandre</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Human septic myopathy: Induction of cyclooxygenase, heme oxygenase and activation of the ubiquitin proteolytic pathway</atitle><jtitle>Anesthesiology (Philadelphia)</jtitle><addtitle>Anesthesiology</addtitle><date>2004-09-01</date><risdate>2004</risdate><volume>101</volume><issue>3</issue><spage>583</spage><epage>590</epage><pages>583-590</pages><issn>0003-3022</issn><eissn>1528-1175</eissn><coden>ANESAV</coden><abstract>Skeletal muscle failure and wasting are manifestations of sepsis in humans that leads to serious and prolonged complications. The authors investigated the role of the major proinflammatory and antiinflammatory pathways, namely the inducible isoforms cyclooxygenase (COX-2) and heme oxygenase (HO-1), and the ubiquitin proteolytic pathway in skeletal muscle of septic patients.
Protein expression was detected by Western blot techniques. Muscle biopsies were taken from two muscle groups, rectus abdominis and vastus lateralis, of septic and control patients.
The study showed an increase in COX-2 and HO-1 proteins expression and an activation of the proteolytic ubiquitin pathway with a parallel increase in free ubiquitin and ubiquitinated proteins in skeletal muscle of septic but not of control patients. In addition, those patients who would die from septic shock expressed more COX-2 and HO-1 proteins in muscle biopsies than did those patients who would survive.
This study showed a marked involvement of local proinflammatory and antiinflammatory pathways and, more importantly, demonstrated the existence of an active ubiquitin proteolytic pathway in skeletal muscle of septic patients. Activation of ubiquitin pathway could be involved in sepsis-related muscle catabolism and wasting.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott</pub><pmid>15329582</pmid><doi>10.1097/00000542-200409000-00006</doi><tpages>8</tpages></addata></record> |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Journals@Ovid Complete |
subjects | Adult Aged Aged, 80 and over Anesthesia Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Biological and medical sciences Blotting, Western Cyclooxygenase 1 Cyclooxygenase 2 Endopeptidases - metabolism Enzyme Induction - physiology Female Heme Oxygenase (Decyclizing) - biosynthesis Humans Immunohistochemistry Isoenzymes - biosynthesis Isoenzymes - genetics Male Medical sciences Membrane Proteins Middle Aged Muscular Diseases - enzymology Muscular Diseases - etiology Muscular Diseases - metabolism Prostaglandin-Endoperoxide Synthases - biosynthesis Prostaglandin-Endoperoxide Synthases - genetics Sepsis - complications Sepsis - enzymology Sepsis - metabolism Ubiquitin - metabolism |
title | Human septic myopathy: Induction of cyclooxygenase, heme oxygenase and activation of the ubiquitin proteolytic pathway |
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