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
Hauptverfasser: Morio, Hiroshi, Saito, Hiroyuki, Hirai, Aizan, Tamura, Yasushi, Yoshida, Sho
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container_end_page 45
container_issue 1
container_start_page 41
container_title Journal of Atherosclerosis and Thrombosis
container_volume 2
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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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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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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