Fixing the leak: targeting the vascular endothelium in sepsis
Angiopoietin-1 is a Tie-2 receptor agonist that stabilizes vascular endothelium, promoting endothelial maturation and preventing capillary leak. Angiopoietin-2 is largely a competitive partial antagonist that is markedly elevated in humans and animal models of sepsis and other inflammatory states, d...
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Veröffentlicht in: | Critical care (London, England) England), 2012-01, Vol.16 (6), p.177-177 |
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description | Angiopoietin-1 is a Tie-2 receptor agonist that stabilizes vascular endothelium, promoting endothelial maturation and preventing capillary leak. Angiopoietin-2 is largely a competitive partial antagonist that is markedly elevated in humans and animal models of sepsis and other inflammatory states, directly disrupts the endothelial barrier, and has been correlated with end-organ dysfunction and death in sepsis. In the previous issue of Critical Care, Alfieri and colleagues used intravital microscopy to study the microvasculature in a murine model of sepsis. Treatment with a modified angiopoietin-1 molecule led to reversal of albumin vascular leak and improved blood flow to skeletal muscle, as well as a decrease in the levels of several inflammatory cytokines. Importantly, the angiopoietin-1 variant was administered 20 hours after initial lipopolysaccharide challenge. This study adds to the evidence that the angiopoietin/Tie-2 axis represents a modifiable pathway through which targeted therapy may be able to directly reverse part of the pathology of sepsis. |
doi_str_mv | 10.1186/cc11829 |
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Angiopoietin-2 is largely a competitive partial antagonist that is markedly elevated in humans and animal models of sepsis and other inflammatory states, directly disrupts the endothelial barrier, and has been correlated with end-organ dysfunction and death in sepsis. In the previous issue of Critical Care, Alfieri and colleagues used intravital microscopy to study the microvasculature in a murine model of sepsis. Treatment with a modified angiopoietin-1 molecule led to reversal of albumin vascular leak and improved blood flow to skeletal muscle, as well as a decrease in the levels of several inflammatory cytokines. Importantly, the angiopoietin-1 variant was administered 20 hours after initial lipopolysaccharide challenge. This study adds to the evidence that the angiopoietin/Tie-2 axis represents a modifiable pathway through which targeted therapy may be able to directly reverse part of the pathology of sepsis.</description><identifier>ISSN: 1364-8535</identifier><identifier>EISSN: 1466-609X</identifier><identifier>DOI: 10.1186/cc11829</identifier><identifier>PMID: 23171759</identifier><language>eng</language><publisher>England: BioMed Central</publisher><subject>Angiopoietin-1 - administration & dosage ; Angiopoietin-1 - genetics ; Animals ; Disease Models, Animal ; Genetic Variation - genetics ; Humans ; Male ; Microcirculation - physiology ; Sepsis - drug therapy ; Sepsis - genetics</subject><ispartof>Critical care (London, England), 2012-01, Vol.16 (6), p.177-177</ispartof><rights>Copyright ©2012 BioMed Central Ltd 2012 BioMed Central Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c402t-772d8034ebac89095d7c9b9af0cafbaa92b0362bfd53726656b1c575565378373</citedby><cites>FETCH-LOGICAL-c402t-772d8034ebac89095d7c9b9af0cafbaa92b0362bfd53726656b1c575565378373</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3672578/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3672578/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23171759$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Spicer, Aaron</creatorcontrib><creatorcontrib>Calfee, Carolyn S</creatorcontrib><title>Fixing the leak: targeting the vascular endothelium in sepsis</title><title>Critical care (London, England)</title><addtitle>Crit Care</addtitle><description>Angiopoietin-1 is a Tie-2 receptor agonist that stabilizes vascular endothelium, promoting endothelial maturation and preventing capillary leak. Angiopoietin-2 is largely a competitive partial antagonist that is markedly elevated in humans and animal models of sepsis and other inflammatory states, directly disrupts the endothelial barrier, and has been correlated with end-organ dysfunction and death in sepsis. In the previous issue of Critical Care, Alfieri and colleagues used intravital microscopy to study the microvasculature in a murine model of sepsis. Treatment with a modified angiopoietin-1 molecule led to reversal of albumin vascular leak and improved blood flow to skeletal muscle, as well as a decrease in the levels of several inflammatory cytokines. Importantly, the angiopoietin-1 variant was administered 20 hours after initial lipopolysaccharide challenge. This study adds to the evidence that the angiopoietin/Tie-2 axis represents a modifiable pathway through which targeted therapy may be able to directly reverse part of the pathology of sepsis.</description><subject>Angiopoietin-1 - administration & dosage</subject><subject>Angiopoietin-1 - genetics</subject><subject>Animals</subject><subject>Disease Models, Animal</subject><subject>Genetic Variation - genetics</subject><subject>Humans</subject><subject>Male</subject><subject>Microcirculation - physiology</subject><subject>Sepsis - drug therapy</subject><subject>Sepsis - genetics</subject><issn>1364-8535</issn><issn>1466-609X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkFtLxDAQhYMo7rqK_0D6pi_VXJqkERRkcVVY8EXBt5CmaTeatmvSLvrvjewFfZqZMx9nhgPAKYKXCOXsSutYsNgDY5QxljIo3vZjT1iW5pTQETgK4R1CxHNGDsEIE8QRp2IMbmb2y7Z10i9M4oz6uE565WvTb7WVCnpwyiemLbsoODs0iW2TYJbBhmNwUCkXzMmmTsDr7P5l-pjOnx-epnfzVGcQ9ynnuMwhyUyhdC6goCXXohCqglpVhVICF5AwXFQlJRwzRlmBNOWUsjjnhJMJuF37LoeiMaU2be-Vk0tvG-W_Zaes_L9p7ULW3UoSxjGNFhNwsTHw3edgQi8bG7RxTrWmG4JElCKCOcpgRM_XqPZdCN5UuzMIyt-w5SbsSJ79_WrHbdMlP_b-egs</recordid><startdate>20120101</startdate><enddate>20120101</enddate><creator>Spicer, Aaron</creator><creator>Calfee, Carolyn S</creator><general>BioMed Central</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><scope>5PM</scope></search><sort><creationdate>20120101</creationdate><title>Fixing the leak: targeting the vascular endothelium in sepsis</title><author>Spicer, Aaron ; Calfee, Carolyn S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c402t-772d8034ebac89095d7c9b9af0cafbaa92b0362bfd53726656b1c575565378373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Angiopoietin-1 - administration & dosage</topic><topic>Angiopoietin-1 - genetics</topic><topic>Animals</topic><topic>Disease Models, Animal</topic><topic>Genetic Variation - genetics</topic><topic>Humans</topic><topic>Male</topic><topic>Microcirculation - physiology</topic><topic>Sepsis - drug therapy</topic><topic>Sepsis - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Spicer, Aaron</creatorcontrib><creatorcontrib>Calfee, Carolyn S</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Critical care (London, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Spicer, Aaron</au><au>Calfee, Carolyn S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fixing the leak: targeting the vascular endothelium in sepsis</atitle><jtitle>Critical care (London, England)</jtitle><addtitle>Crit Care</addtitle><date>2012-01-01</date><risdate>2012</risdate><volume>16</volume><issue>6</issue><spage>177</spage><epage>177</epage><pages>177-177</pages><issn>1364-8535</issn><eissn>1466-609X</eissn><abstract>Angiopoietin-1 is a Tie-2 receptor agonist that stabilizes vascular endothelium, promoting endothelial maturation and preventing capillary leak. Angiopoietin-2 is largely a competitive partial antagonist that is markedly elevated in humans and animal models of sepsis and other inflammatory states, directly disrupts the endothelial barrier, and has been correlated with end-organ dysfunction and death in sepsis. In the previous issue of Critical Care, Alfieri and colleagues used intravital microscopy to study the microvasculature in a murine model of sepsis. Treatment with a modified angiopoietin-1 molecule led to reversal of albumin vascular leak and improved blood flow to skeletal muscle, as well as a decrease in the levels of several inflammatory cytokines. Importantly, the angiopoietin-1 variant was administered 20 hours after initial lipopolysaccharide challenge. 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subjects | Angiopoietin-1 - administration & dosage Angiopoietin-1 - genetics Animals Disease Models, Animal Genetic Variation - genetics Humans Male Microcirculation - physiology Sepsis - drug therapy Sepsis - genetics |
title | Fixing the leak: targeting the vascular endothelium in sepsis |
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