The variation of plasma concentrations of a novel, adipocyte derived protein, adiponectin, in patients with acute myocardial infarction
Adiponectin is a new member of adipocyte derived proteins belonging to the soluble defence collagens. 1 Plasma adiponectin concentrations in obese subjects are decreased in spite of an adipose specific expression. 1 More interestingly, the patients with chronic coronary artery disease exhibited lowe...
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| Veröffentlicht in: | British heart journal 2003-06, Vol.89 (6), p.667-667 |
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| creator | Kojima, S Funahashi, T Sakamoto, T Miyamoto, S Soejima, H Hokamaki, J Kajiwara, I Sugiyama, S Yoshimura, M Fujimoto, K Miyao, Y Suefuji, H Kitagawa, A Ouchi, N Kihara, S Matsuzawa, Y Ogawa, H |
| description | Adiponectin is a new member of adipocyte derived proteins belonging to the soluble defence collagens. 1 Plasma adiponectin concentrations in obese subjects are decreased in spite of an adipose specific expression. 1 More interestingly, the patients with chronic coronary artery disease exhibited lower plasma adiponectin concentrations compared to body mass index (BMI) matched control subjects. 2 On the other hand, adiponectin accumulates in the vascular subendothelial space when the endothelial barrier is damaged. 3 In vitro, adiponectin suppresses the expression of adhesion molecules in the vascular endothelial cells and cytokine production from macrophages. 2, 4 Therefore, the molecule may be involved in the inflammation and tissue repairing processes. Active inflammation and accumulation of activated monocyte derived macrophages secreting cytokines, chemokines, growth regulating molecules, and metalloproteinases were observed at the site of coronary plaque rupture in acute coronary syndrome. 5 Adiponectin inhibits the expression of vascular cell adhesion molecule-1, endothelial leucocyte adhesion molecule-1, and intracellular adhesion molecule-1, which are detected in human atherosclerotic lesions, through the inactivation of tumour necrosis factor α (TNFα). |
| doi_str_mv | 10.1136/heart.89.6.667 |
| format | Article |
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Active inflammation and accumulation of activated monocyte derived macrophages secreting cytokines, chemokines, growth regulating molecules, and metalloproteinases were observed at the site of coronary plaque rupture in acute coronary syndrome. 5 Adiponectin inhibits the expression of vascular cell adhesion molecule-1, endothelial leucocyte adhesion molecule-1, and intracellular adhesion molecule-1, which are detected in human atherosclerotic lesions, through the inactivation of tumour necrosis factor α (TNFα).</description><identifier>ISSN: 1355-6037</identifier><identifier>ISSN: 0007-0769</identifier><identifier>EISSN: 1468-201X</identifier><identifier>DOI: 10.1136/heart.89.6.667</identifier><identifier>PMID: 12748233</identifier><language>eng</language><publisher>England: BMJ Publishing Group Ltd and British Cardiovascular Society</publisher><subject>Acute coronary syndromes ; acute myocardial infarction ; adinopectin ; Adipocytes ; Adipocytes - metabolism ; Adiponectin ; AMI ; Angioplasty ; Biomarkers - blood ; BMI ; Body Mass Index ; C reactive protein ; C-Reactive Protein - analysis ; Cardiac patients ; Cardiovascular disease ; Coronary vessels ; CRP ; Fat cells ; Heart attack ; Heart attacks ; Humans ; Identification and classification ; Intercellular Signaling Peptides and Proteins ; Medical imaging ; Myocardial Infarction - blood ; Physiological aspects ; Plasma ; Proteins ; Proteins - metabolism ; Rodents ; Scientific Letters ; Thrombosis ; TNFα ; tumour necrosis factor α</subject><ispartof>British heart journal, 2003-06, Vol.89 (6), p.667-667</ispartof><rights>Copyright 2003 by Heart</rights><rights>COPYRIGHT 2003 BMJ Publishing Group Ltd.</rights><rights>Copyright: 2003 Copyright 2003 by Heart</rights><rights>Copyright © Copyright 2003 by Heart 2003</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b563t-7fdae36782f15eddfc8bb0007052f818716e8f5b6542a659ba6e7869eb79b92b3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1767676/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1767676/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,315,728,781,785,886,27929,27930,53796,53798</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12748233$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kojima, S</creatorcontrib><creatorcontrib>Funahashi, T</creatorcontrib><creatorcontrib>Sakamoto, T</creatorcontrib><creatorcontrib>Miyamoto, S</creatorcontrib><creatorcontrib>Soejima, H</creatorcontrib><creatorcontrib>Hokamaki, J</creatorcontrib><creatorcontrib>Kajiwara, I</creatorcontrib><creatorcontrib>Sugiyama, S</creatorcontrib><creatorcontrib>Yoshimura, M</creatorcontrib><creatorcontrib>Fujimoto, K</creatorcontrib><creatorcontrib>Miyao, Y</creatorcontrib><creatorcontrib>Suefuji, H</creatorcontrib><creatorcontrib>Kitagawa, A</creatorcontrib><creatorcontrib>Ouchi, N</creatorcontrib><creatorcontrib>Kihara, S</creatorcontrib><creatorcontrib>Matsuzawa, Y</creatorcontrib><creatorcontrib>Ogawa, H</creatorcontrib><title>The variation of plasma concentrations of a novel, adipocyte derived protein, adiponectin, in patients with acute myocardial infarction</title><title>British heart journal</title><addtitle>Heart</addtitle><description>Adiponectin is a new member of adipocyte derived proteins belonging to the soluble defence collagens. 1 Plasma adiponectin concentrations in obese subjects are decreased in spite of an adipose specific expression. 1 More interestingly, the patients with chronic coronary artery disease exhibited lower plasma adiponectin concentrations compared to body mass index (BMI) matched control subjects. 2 On the other hand, adiponectin accumulates in the vascular subendothelial space when the endothelial barrier is damaged. 3 In vitro, adiponectin suppresses the expression of adhesion molecules in the vascular endothelial cells and cytokine production from macrophages. 2, 4 Therefore, the molecule may be involved in the inflammation and tissue repairing processes. Active inflammation and accumulation of activated monocyte derived macrophages secreting cytokines, chemokines, growth regulating molecules, and metalloproteinases were observed at the site of coronary plaque rupture in acute coronary syndrome. 5 Adiponectin inhibits the expression of vascular cell adhesion molecule-1, endothelial leucocyte adhesion molecule-1, and intracellular adhesion molecule-1, which are detected in human atherosclerotic lesions, through the inactivation of tumour necrosis factor α (TNFα).</description><subject>Acute coronary syndromes</subject><subject>acute myocardial infarction</subject><subject>adinopectin</subject><subject>Adipocytes</subject><subject>Adipocytes - metabolism</subject><subject>Adiponectin</subject><subject>AMI</subject><subject>Angioplasty</subject><subject>Biomarkers - blood</subject><subject>BMI</subject><subject>Body Mass Index</subject><subject>C reactive protein</subject><subject>C-Reactive Protein - analysis</subject><subject>Cardiac patients</subject><subject>Cardiovascular disease</subject><subject>Coronary vessels</subject><subject>CRP</subject><subject>Fat cells</subject><subject>Heart attack</subject><subject>Heart attacks</subject><subject>Humans</subject><subject>Identification and classification</subject><subject>Intercellular Signaling Peptides and Proteins</subject><subject>Medical imaging</subject><subject>Myocardial Infarction - blood</subject><subject>Physiological aspects</subject><subject>Plasma</subject><subject>Proteins</subject><subject>Proteins - metabolism</subject><subject>Rodents</subject><subject>Scientific Letters</subject><subject>Thrombosis</subject><subject>TNFα</subject><subject>tumour necrosis factor α</subject><issn>1355-6037</issn><issn>0007-0769</issn><issn>1468-201X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqFkl2L1DAUhoso7ofeeikBQRDsmPQjSW8WlsF11VVBVvEupOnpTMY2qUln1vkF_m1Pd4ZdFVFy0STned_Tc3KS5BGjM8Zy_mIJOowzWc34jHNxJzlkBZdpRtmXu7jPyzLlNBcHyVGMK0ppUUl-PzlgmShklueHyY_LJZCNDlaP1jviWzJ0OvaaGO8MuDFc38cpoInzG-ieE93YwZvtCKSBYDfQkCH4EazbhxyYcTpYRwaUo0skV3ZcEm3WKOq33ujQWN0h0epgpgwPknut7iI83H-Pk09nLy_n5-nFh1ev56cXaV3yfExF22jIuZBZy0pomtbIusa6BC2zVjIpGAfZljUvi0zzsqo1ByF5BbWo6iqr8-PkZOc7rOseml2JnRqC7XXYKq-t-j3i7FIt_EYxwaeFBk_3BsF_W0McVW-jga7TDvw6KpFnkgo-gU_-AFd-HRwWh16IVJIWFKl0Ry10Bwr74TGrWYADTI6dbC1enzKKDyZ4wZCf_YXH1UBvzb8EJvgYA7Q3tTKqphFS1yOkZKW4whFCweNfO3SL72fm9pdtHOH7TVyHrwrlolTvP8-VfPNOnn884-ot8s92fN2v_pf8JxOc4l4</recordid><startdate>200306</startdate><enddate>200306</enddate><creator>Kojima, S</creator><creator>Funahashi, T</creator><creator>Sakamoto, T</creator><creator>Miyamoto, S</creator><creator>Soejima, H</creator><creator>Hokamaki, J</creator><creator>Kajiwara, I</creator><creator>Sugiyama, S</creator><creator>Yoshimura, M</creator><creator>Fujimoto, K</creator><creator>Miyao, Y</creator><creator>Suefuji, H</creator><creator>Kitagawa, A</creator><creator>Ouchi, N</creator><creator>Kihara, S</creator><creator>Matsuzawa, Y</creator><creator>Ogawa, H</creator><general>BMJ Publishing Group Ltd and British Cardiovascular Society</general><general>BMJ Publishing Group Ltd</general><general>BMJ Publishing Group LTD</general><general>Copyright 2003 by Heart</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>200306</creationdate><title>The variation of plasma concentrations of a novel, adipocyte derived protein, adiponectin, in patients with acute myocardial infarction</title><author>Kojima, S ; Funahashi, T ; Sakamoto, T ; Miyamoto, S ; Soejima, H ; Hokamaki, J ; Kajiwara, I ; Sugiyama, S ; Yoshimura, M ; Fujimoto, K ; Miyao, Y ; Suefuji, H ; Kitagawa, A ; Ouchi, N ; Kihara, S ; Matsuzawa, Y ; Ogawa, H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b563t-7fdae36782f15eddfc8bb0007052f818716e8f5b6542a659ba6e7869eb79b92b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Acute coronary syndromes</topic><topic>acute myocardial infarction</topic><topic>adinopectin</topic><topic>Adipocytes</topic><topic>Adipocytes - metabolism</topic><topic>Adiponectin</topic><topic>AMI</topic><topic>Angioplasty</topic><topic>Biomarkers - blood</topic><topic>BMI</topic><topic>Body Mass Index</topic><topic>C reactive protein</topic><topic>C-Reactive Protein - analysis</topic><topic>Cardiac patients</topic><topic>Cardiovascular disease</topic><topic>Coronary vessels</topic><topic>CRP</topic><topic>Fat cells</topic><topic>Heart attack</topic><topic>Heart attacks</topic><topic>Humans</topic><topic>Identification and classification</topic><topic>Intercellular Signaling Peptides and Proteins</topic><topic>Medical imaging</topic><topic>Myocardial Infarction - blood</topic><topic>Physiological aspects</topic><topic>Plasma</topic><topic>Proteins</topic><topic>Proteins - metabolism</topic><topic>Rodents</topic><topic>Scientific Letters</topic><topic>Thrombosis</topic><topic>TNFα</topic><topic>tumour necrosis factor α</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kojima, S</creatorcontrib><creatorcontrib>Funahashi, T</creatorcontrib><creatorcontrib>Sakamoto, T</creatorcontrib><creatorcontrib>Miyamoto, S</creatorcontrib><creatorcontrib>Soejima, H</creatorcontrib><creatorcontrib>Hokamaki, J</creatorcontrib><creatorcontrib>Kajiwara, I</creatorcontrib><creatorcontrib>Sugiyama, S</creatorcontrib><creatorcontrib>Yoshimura, M</creatorcontrib><creatorcontrib>Fujimoto, K</creatorcontrib><creatorcontrib>Miyao, Y</creatorcontrib><creatorcontrib>Suefuji, H</creatorcontrib><creatorcontrib>Kitagawa, A</creatorcontrib><creatorcontrib>Ouchi, N</creatorcontrib><creatorcontrib>Kihara, S</creatorcontrib><creatorcontrib>Matsuzawa, Y</creatorcontrib><creatorcontrib>Ogawa, H</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>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>British heart journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kojima, S</au><au>Funahashi, T</au><au>Sakamoto, T</au><au>Miyamoto, S</au><au>Soejima, H</au><au>Hokamaki, J</au><au>Kajiwara, I</au><au>Sugiyama, S</au><au>Yoshimura, M</au><au>Fujimoto, K</au><au>Miyao, Y</au><au>Suefuji, H</au><au>Kitagawa, A</au><au>Ouchi, N</au><au>Kihara, S</au><au>Matsuzawa, Y</au><au>Ogawa, H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The variation of plasma concentrations of a novel, adipocyte derived protein, adiponectin, in patients with acute myocardial infarction</atitle><jtitle>British heart journal</jtitle><addtitle>Heart</addtitle><date>2003-06</date><risdate>2003</risdate><volume>89</volume><issue>6</issue><spage>667</spage><epage>667</epage><pages>667-667</pages><issn>1355-6037</issn><issn>0007-0769</issn><eissn>1468-201X</eissn><abstract>Adiponectin is a new member of adipocyte derived proteins belonging to the soluble defence collagens. 1 Plasma adiponectin concentrations in obese subjects are decreased in spite of an adipose specific expression. 1 More interestingly, the patients with chronic coronary artery disease exhibited lower plasma adiponectin concentrations compared to body mass index (BMI) matched control subjects. 2 On the other hand, adiponectin accumulates in the vascular subendothelial space when the endothelial barrier is damaged. 3 In vitro, adiponectin suppresses the expression of adhesion molecules in the vascular endothelial cells and cytokine production from macrophages. 2, 4 Therefore, the molecule may be involved in the inflammation and tissue repairing processes. Active inflammation and accumulation of activated monocyte derived macrophages secreting cytokines, chemokines, growth regulating molecules, and metalloproteinases were observed at the site of coronary plaque rupture in acute coronary syndrome. 5 Adiponectin inhibits the expression of vascular cell adhesion molecule-1, endothelial leucocyte adhesion molecule-1, and intracellular adhesion molecule-1, which are detected in human atherosclerotic lesions, through the inactivation of tumour necrosis factor α (TNFα).</abstract><cop>England</cop><pub>BMJ Publishing Group Ltd and British Cardiovascular Society</pub><pmid>12748233</pmid><doi>10.1136/heart.89.6.667</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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| subjects | Acute coronary syndromes acute myocardial infarction adinopectin Adipocytes Adipocytes - metabolism Adiponectin AMI Angioplasty Biomarkers - blood BMI Body Mass Index C reactive protein C-Reactive Protein - analysis Cardiac patients Cardiovascular disease Coronary vessels CRP Fat cells Heart attack Heart attacks Humans Identification and classification Intercellular Signaling Peptides and Proteins Medical imaging Myocardial Infarction - blood Physiological aspects Plasma Proteins Proteins - metabolism Rodents Scientific Letters Thrombosis TNFα tumour necrosis factor α |
| title | The variation of plasma concentrations of a novel, adipocyte derived protein, adiponectin, in patients with acute myocardial infarction |
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