Oleic acid induces endothelin-1 expression through activation of protein kinase C and NF-κB
被引:46
作者:
Park, JY
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机构:Univ Ulsan, Coll Med, Dept Internal Med, Songpa Ku, Seoul 138736, South Korea
Park, JY
Kim, YM
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机构:Univ Ulsan, Coll Med, Dept Internal Med, Songpa Ku, Seoul 138736, South Korea
Kim, YM
Song, HS
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机构:Univ Ulsan, Coll Med, Dept Internal Med, Songpa Ku, Seoul 138736, South Korea
Song, HS
Park, KY
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机构:Univ Ulsan, Coll Med, Dept Internal Med, Songpa Ku, Seoul 138736, South Korea
Park, KY
Kim, YM
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机构:Univ Ulsan, Coll Med, Dept Internal Med, Songpa Ku, Seoul 138736, South Korea
Kim, YM
Kim, MS
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机构:Univ Ulsan, Coll Med, Dept Internal Med, Songpa Ku, Seoul 138736, South Korea
Kim, MS
Pak, YK
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机构:Univ Ulsan, Coll Med, Dept Internal Med, Songpa Ku, Seoul 138736, South Korea
Pak, YK
Lee, IK
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机构:Univ Ulsan, Coll Med, Dept Internal Med, Songpa Ku, Seoul 138736, South Korea
Lee, IK
Lee, JD
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机构:Univ Ulsan, Coll Med, Dept Internal Med, Songpa Ku, Seoul 138736, South Korea
Lee, JD
Park, SJ
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机构:Univ Ulsan, Coll Med, Dept Internal Med, Songpa Ku, Seoul 138736, South Korea
Park, SJ
Lee, KU
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机构:
Univ Ulsan, Coll Med, Dept Internal Med, Songpa Ku, Seoul 138736, South KoreaUniv Ulsan, Coll Med, Dept Internal Med, Songpa Ku, Seoul 138736, South Korea
Lee, KU
[1
]
机构:
[1] Univ Ulsan, Coll Med, Dept Internal Med, Songpa Ku, Seoul 138736, South Korea
[2] Univ Ulsan, Asan Inst Life Sci, Seoul 138736, South Korea
[3] Keimyung Univ, Sch Med, Dept Internal Med, Taegu 700712, South Korea
[4] Univ Ulsan, Coll Med, Dept Biochem, Seoul 138736, South Korea
endothelin-1;
oleic acid;
protein kinase C;
nuclear factor kappa B;
D O I:
10.1016/S0006-291X(03)00436-4
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
This study investigated the effect of oleic acid on the expression levels of endothelin-1 (ET-1) and on the signaling pathways mediating it in human aortic endothelial cells (HAECs). ET-1 mRNA expression was significantly increased by oleic acid in a dose-and time-dependent manner. Elevation of ET-I expression in response to oleic acid was inhibited by the protein kinase C (PKC) inhibitor, GF109203X, or the NF-kappabeta inhibitor, pyrrolidine dithiocarbamate. In addition, both PKC and NF-kappabeta activities were significantly increased by oleic acid. Immunoblot analysis revealed that conventional PKCs (PKC-alpha and -betaII isoforms) were significantly increased in the membranous fractions of HAECs treated with oleic acid. PKC inhibitor completely abolished oleic acid-induced NF-kappabeta activation, suggesting that PKC activation is upstream of NF-kappabeta activation in oleic acid-induced ET-1 expression. These data suggest that elevated plasma oleic acid levels observed in obese, insulin-resistant subjects result in endothelial dysfunction, at least in part, through an increase in ET-1 expression. (C) 2003 Elsevier Science (USA). All rights reserved.