Effect of Modified LDL on the Release of NO and PGI2 from Rat Peritoneal Macrophages
Nitric oxide (NO) and prostacyclin (PGI2) have vasodilative and anti-proliferative effects on smooth muscle cells (SMC) and an anti-aggregating action on platelets. The present study was designed to elucidate the influence of modified low density lipoprotein (LDL) on the release of NO and PGI2 from...
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Veröffentlicht in: | Journal of Atherosclerosis and Thrombosis 1995, Vol.2(1), pp.41-45 |
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creator | Morio, Hiroshi Saito, Hiroyuki Hirai, Aizan Tamura, Yasushi Yoshida, Sho |
description | Nitric oxide (NO) and prostacyclin (PGI2) have vasodilative and anti-proliferative effects on smooth muscle cells (SMC) and an anti-aggregating action on platelets. The present study was designed to elucidate the influence of modified low density lipoprotein (LDL) on the release of NO and PGI2 from rat peritoneal macrophages. Cholesteryl ester (CE) content in macrophages markedly increased on incubation with acetylated LDL (ac-LDL), while NO release did not change. Although incubation with mildly oxidized LDL (m-ox-LDL) and highly oxidized LDL (h-ox-LDL) increased CE content in macrophages, only incubation with h-ox-LDL reduced NO release. PGI2 release from macrophages was not affected by incubation with ac-LDL, m-ox-LDL or h-ox-LDL. These results indicate that the degree of suppression of NO release in macrophages by modified LDL is related to the extent of oxidative modification of LDL itself, but not to the extent of the accumulation of CE in macrophages. Although the role of NO released from macrophages in atherosclerosis is still unclear, the observation of reduced production of NO from macrophages in response to ox-LDL may provide new insight into the role of ox-LDL in the pathogenesis of atherosclerosis. J Atheroscler Thromb, 1995 ; 2 : 41-45. |
doi_str_mv | 10.5551/jat1994.2.41 |
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The present study was designed to elucidate the influence of modified low density lipoprotein (LDL) on the release of NO and PGI2 from rat peritoneal macrophages. Cholesteryl ester (CE) content in macrophages markedly increased on incubation with acetylated LDL (ac-LDL), while NO release did not change. Although incubation with mildly oxidized LDL (m-ox-LDL) and highly oxidized LDL (h-ox-LDL) increased CE content in macrophages, only incubation with h-ox-LDL reduced NO release. PGI2 release from macrophages was not affected by incubation with ac-LDL, m-ox-LDL or h-ox-LDL. These results indicate that the degree of suppression of NO release in macrophages by modified LDL is related to the extent of oxidative modification of LDL itself, but not to the extent of the accumulation of CE in macrophages. Although the role of NO released from macrophages in atherosclerosis is still unclear, the observation of reduced production of NO from macrophages in response to ox-LDL may provide new insight into the role of ox-LDL in the pathogenesis of atherosclerosis. 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The present study was designed to elucidate the influence of modified low density lipoprotein (LDL) on the release of NO and PGI2 from rat peritoneal macrophages. Cholesteryl ester (CE) content in macrophages markedly increased on incubation with acetylated LDL (ac-LDL), while NO release did not change. Although incubation with mildly oxidized LDL (m-ox-LDL) and highly oxidized LDL (h-ox-LDL) increased CE content in macrophages, only incubation with h-ox-LDL reduced NO release. PGI2 release from macrophages was not affected by incubation with ac-LDL, m-ox-LDL or h-ox-LDL. These results indicate that the degree of suppression of NO release in macrophages by modified LDL is related to the extent of oxidative modification of LDL itself, but not to the extent of the accumulation of CE in macrophages. Although the role of NO released from macrophages in atherosclerosis is still unclear, the observation of reduced production of NO from macrophages in response to ox-LDL may provide new insight into the role of ox-LDL in the pathogenesis of atherosclerosis. J Atheroscler Thromb, 1995 ; 2 : 41-45.</description><subject>Animals</subject><subject>Cells, Cultured</subject><subject>Cholesterol Esters - metabolism</subject><subject>Epoprostenol - metabolism</subject><subject>Lipoproteins, LDL - pharmacology</subject><subject>Macrophages, Peritoneal - metabolism</subject><subject>Male</subject><subject>Nitric Oxide - metabolism</subject><subject>Rats</subject><subject>Rats, Wistar</subject><issn>1340-3478</issn><issn>1880-3873</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkM1Lw0AQxRdR6ufNq7AnT7buZ5K9KfUTWltKPS-TzaxNSZO6mx78701tKR6GefB7PGYeIdecDbTW_H4JLTdGDcRA8SNyxrOM9WWWyuNOS9VplWan5DzGJWNSai16pGeE0IKlZ2T-7D26ljaejpui9CUWdPQ0ok1N2wXSGVYIEbf4Y0KhLuj09V1QH5oVnUFLpxjKtqkRKjoGF5r1Ar4wXpITD1XEq_2-IJ8vz_PhW380eX0fPo76TiaC94F57xwXrsDMKadZBh5yrZPCGA0CnBE610rmiZCJMWnOE8ULXaTgmE-4lhfkdpe7Ds33BmNrV2V0WFVQY7OJNk1N0tWxNd7tjN2JMQb0dh3KFYQfy5ndlmj3JVphFe_sN_vcTb7C4mDet9bxhx1fxrb798AhtKWr8F8Y_xvFD8gtIFis5S8erII4</recordid><startdate>1995</startdate><enddate>1995</enddate><creator>Morio, Hiroshi</creator><creator>Saito, Hiroyuki</creator><creator>Hirai, Aizan</creator><creator>Tamura, Yasushi</creator><creator>Yoshida, Sho</creator><general>Japan Atherosclerosis 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>1995</creationdate><title>Effect of Modified LDL on the Release of NO and PGI2 from Rat Peritoneal Macrophages</title><author>Morio, Hiroshi ; Saito, Hiroyuki ; Hirai, Aizan ; Tamura, Yasushi ; Yoshida, Sho</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3621-a0ffcc12cde8c4c508afab556d995a2ac925b543b6236997b1641d5d7ac0f6153</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Animals</topic><topic>Cells, Cultured</topic><topic>Cholesterol Esters - metabolism</topic><topic>Epoprostenol - metabolism</topic><topic>Lipoproteins, LDL - pharmacology</topic><topic>Macrophages, Peritoneal - metabolism</topic><topic>Male</topic><topic>Nitric Oxide - metabolism</topic><topic>Rats</topic><topic>Rats, Wistar</topic><toplevel>online_resources</toplevel><creatorcontrib>Morio, Hiroshi</creatorcontrib><creatorcontrib>Saito, Hiroyuki</creatorcontrib><creatorcontrib>Hirai, Aizan</creatorcontrib><creatorcontrib>Tamura, Yasushi</creatorcontrib><creatorcontrib>Yoshida, Sho</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>Journal of Atherosclerosis and Thrombosis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Morio, Hiroshi</au><au>Saito, Hiroyuki</au><au>Hirai, Aizan</au><au>Tamura, Yasushi</au><au>Yoshida, Sho</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of Modified LDL on the Release of NO and PGI2 from Rat Peritoneal Macrophages</atitle><jtitle>Journal of Atherosclerosis and Thrombosis</jtitle><addtitle>JAT</addtitle><date>1995</date><risdate>1995</risdate><volume>2</volume><issue>1</issue><spage>41</spage><epage>45</epage><pages>41-45</pages><issn>1340-3478</issn><eissn>1880-3873</eissn><abstract>Nitric oxide (NO) and prostacyclin (PGI2) have vasodilative and anti-proliferative effects on smooth muscle cells (SMC) and an anti-aggregating action on platelets. The present study was designed to elucidate the influence of modified low density lipoprotein (LDL) on the release of NO and PGI2 from rat peritoneal macrophages. Cholesteryl ester (CE) content in macrophages markedly increased on incubation with acetylated LDL (ac-LDL), while NO release did not change. Although incubation with mildly oxidized LDL (m-ox-LDL) and highly oxidized LDL (h-ox-LDL) increased CE content in macrophages, only incubation with h-ox-LDL reduced NO release. PGI2 release from macrophages was not affected by incubation with ac-LDL, m-ox-LDL or h-ox-LDL. These results indicate that the degree of suppression of NO release in macrophages by modified LDL is related to the extent of oxidative modification of LDL itself, but not to the extent of the accumulation of CE in macrophages. Although the role of NO released from macrophages in atherosclerosis is still unclear, the observation of reduced production of NO from macrophages in response to ox-LDL may provide new insight into the role of ox-LDL in the pathogenesis of atherosclerosis. J Atheroscler Thromb, 1995 ; 2 : 41-45.</abstract><cop>Japan</cop><pub>Japan Atherosclerosis Society</pub><pmid>9225207</pmid><doi>10.5551/jat1994.2.41</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Cells, Cultured Cholesterol Esters - metabolism Epoprostenol - metabolism Lipoproteins, LDL - pharmacology Macrophages, Peritoneal - metabolism Male Nitric Oxide - metabolism Rats Rats, Wistar |
title | Effect of Modified LDL on the Release of NO and PGI2 from Rat Peritoneal Macrophages |
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