Prostacyclin in Vascular Diseases: Recent Insights and Future Perspectives
Prostacyclin (PGI2) is one of the important vascular prostanoids, the effects of which counteract those of thromboxane (TXA2), and these 2 prostanoids provide an important balance in cardiovascular homeostasis. The clinical experience of COX-2 selective inhibitors having unexpected adverse effects i...
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Veröffentlicht in: | Circulation Journal 2010, Vol.74(5), pp.836-843 |
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description | Prostacyclin (PGI2) is one of the important vascular prostanoids, the effects of which counteract those of thromboxane (TXA2), and these 2 prostanoids provide an important balance in cardiovascular homeostasis. The clinical experience of COX-2 selective inhibitors having unexpected adverse effects in patients with cardiovascular risk has opened up a debate about the role of COX-2-derived prostanoids in vascular pathophysiology. PGI2 is a major anti-atherogenic prostanoid produced by COX-2 in vascular cells, including endothelial and vascular smooth muscle cells. The balance between COX-2-derived PGI2, COX-1-derived TXA2, and other COX-2-mediated atherogenic prostanoids is a crucial factor in determining pathophysiological outcomes. Recent studies using stable PGI2 analogs and genetically deficient mice have revealed novel effects of PGI2 on its target cells, such as endothelial and endothelial progenitor cells. The role PGI2 in the physiology and pathophysiology of vascular diseases is reviewed and the recent findings linking PGI2, COX-2 and atherothrombosis are summarized. (Circ J 2010; 74: 836 - 843) |
doi_str_mv | 10.1253/circj.CJ-10-0195 |
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The clinical experience of COX-2 selective inhibitors having unexpected adverse effects in patients with cardiovascular risk has opened up a debate about the role of COX-2-derived prostanoids in vascular pathophysiology. PGI2 is a major anti-atherogenic prostanoid produced by COX-2 in vascular cells, including endothelial and vascular smooth muscle cells. The balance between COX-2-derived PGI2, COX-1-derived TXA2, and other COX-2-mediated atherogenic prostanoids is a crucial factor in determining pathophysiological outcomes. Recent studies using stable PGI2 analogs and genetically deficient mice have revealed novel effects of PGI2 on its target cells, such as endothelial and endothelial progenitor cells. The role PGI2 in the physiology and pathophysiology of vascular diseases is reviewed and the recent findings linking PGI2, COX-2 and atherothrombosis are summarized. 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The clinical experience of COX-2 selective inhibitors having unexpected adverse effects in patients with cardiovascular risk has opened up a debate about the role of COX-2-derived prostanoids in vascular pathophysiology. PGI2 is a major anti-atherogenic prostanoid produced by COX-2 in vascular cells, including endothelial and vascular smooth muscle cells. The balance between COX-2-derived PGI2, COX-1-derived TXA2, and other COX-2-mediated atherogenic prostanoids is a crucial factor in determining pathophysiological outcomes. Recent studies using stable PGI2 analogs and genetically deficient mice have revealed novel effects of PGI2 on its target cells, such as endothelial and endothelial progenitor cells. The role PGI2 in the physiology and pathophysiology of vascular diseases is reviewed and the recent findings linking PGI2, COX-2 and atherothrombosis are summarized. (Circ J 2010; 74: 836 - 843)</description><subject>Animals</subject><subject>Atherosclerosis</subject><subject>Cyclooxygenase</subject><subject>Cyclooxygenase 1 - genetics</subject><subject>Cyclooxygenase 1 - metabolism</subject><subject>Cyclooxygenase 2 Inhibitors - adverse effects</subject><subject>Cyclooxygenase 2 Inhibitors - therapeutic use</subject><subject>Endothelial Cells - metabolism</subject><subject>Endothelial progenitor cells</subject><subject>Epoprostenol - genetics</subject><subject>Epoprostenol - metabolism</subject><subject>Homeostasis</subject><subject>Humans</subject><subject>Membrane Proteins - genetics</subject><subject>Membrane Proteins - metabolism</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>Muscle, Smooth, Vascular - metabolism</subject><subject>Muscle, Smooth, Vascular - physiopathology</subject><subject>Myocytes, Smooth Muscle - metabolism</subject><subject>Prostacyclin</subject><subject>Stem Cells - metabolism</subject><subject>Thrombosis - genetics</subject><subject>Thrombosis - metabolism</subject><subject>Thrombosis - physiopathology</subject><issn>1346-9843</issn><issn>1347-4820</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkD1PwzAQhi0EoqWwM6EyMaWcvxJnRIECVSUYgNW6OA6kSj-wk6H_HqcprXTynaznXp0eQq4pTCiT_N5Uziwm2SyiEAFN5QkZUi6SSCgGp7s5jlIl-IBceL8AYCnI9JwMGAgmOBdDcvvu1r5BszV1tRqH-kJv2hrd-LHyFr31l-SsxNrbq30fkc_p00f2Es3fnl-zh3lkZCybqFA5SzGBogRlueJhUEIVCXCKSpUsj6WyjJUqnCbzxJQxK2JqsBAUkcWWj8hdn7tx69_W-kYvK29sXePKrluvE85TKSmIQEJPmnC7d7bUG1ct0W01Bd150TsvOpt1H52XsHKzD2_zpS0OC_8iAjDtgUWw8W0PALqmMrXdJyZCy-45Jh-BH3TarvgfpLB3BA</recordid><startdate>2010</startdate><enddate>2010</enddate><creator>Kawabe, Jun-ichi</creator><creator>Ushikubi, Fumitaka</creator><creator>Hasebe, Naoyuki</creator><general>The Japanese Circulation Society</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></search><sort><creationdate>2010</creationdate><title>Prostacyclin in Vascular Diseases</title><author>Kawabe, Jun-ichi ; Ushikubi, Fumitaka ; Hasebe, Naoyuki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c565t-d8b29a70df08e3830df848d7031a88f2b658e22f88205b7cf62d61cad41aa26e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Animals</topic><topic>Atherosclerosis</topic><topic>Cyclooxygenase</topic><topic>Cyclooxygenase 1 - genetics</topic><topic>Cyclooxygenase 1 - metabolism</topic><topic>Cyclooxygenase 2 Inhibitors - adverse effects</topic><topic>Cyclooxygenase 2 Inhibitors - therapeutic use</topic><topic>Endothelial Cells - metabolism</topic><topic>Endothelial progenitor cells</topic><topic>Epoprostenol - genetics</topic><topic>Epoprostenol - metabolism</topic><topic>Homeostasis</topic><topic>Humans</topic><topic>Membrane Proteins - genetics</topic><topic>Membrane Proteins - metabolism</topic><topic>Mice</topic><topic>Mice, Knockout</topic><topic>Muscle, Smooth, Vascular - metabolism</topic><topic>Muscle, Smooth, Vascular - physiopathology</topic><topic>Myocytes, Smooth Muscle - metabolism</topic><topic>Prostacyclin</topic><topic>Stem Cells - metabolism</topic><topic>Thrombosis - genetics</topic><topic>Thrombosis - metabolism</topic><topic>Thrombosis - physiopathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kawabe, Jun-ichi</creatorcontrib><creatorcontrib>Ushikubi, Fumitaka</creatorcontrib><creatorcontrib>Hasebe, Naoyuki</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><jtitle>Circulation Journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kawabe, Jun-ichi</au><au>Ushikubi, Fumitaka</au><au>Hasebe, Naoyuki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prostacyclin in Vascular Diseases: Recent Insights and Future Perspectives</atitle><jtitle>Circulation Journal</jtitle><addtitle>Circ J</addtitle><date>2010</date><risdate>2010</risdate><volume>74</volume><issue>5</issue><spage>836</spage><epage>843</epage><pages>836-843</pages><issn>1346-9843</issn><eissn>1347-4820</eissn><abstract>Prostacyclin (PGI2) is one of the important vascular prostanoids, the effects of which counteract those of thromboxane (TXA2), and these 2 prostanoids provide an important balance in cardiovascular homeostasis. 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subjects | Animals Atherosclerosis Cyclooxygenase Cyclooxygenase 1 - genetics Cyclooxygenase 1 - metabolism Cyclooxygenase 2 Inhibitors - adverse effects Cyclooxygenase 2 Inhibitors - therapeutic use Endothelial Cells - metabolism Endothelial progenitor cells Epoprostenol - genetics Epoprostenol - metabolism Homeostasis Humans Membrane Proteins - genetics Membrane Proteins - metabolism Mice Mice, Knockout Muscle, Smooth, Vascular - metabolism Muscle, Smooth, Vascular - physiopathology Myocytes, Smooth Muscle - metabolism Prostacyclin Stem Cells - metabolism Thrombosis - genetics Thrombosis - metabolism Thrombosis - physiopathology |
title | Prostacyclin in Vascular Diseases: Recent Insights and Future Perspectives |
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