期刊论文详细信息
Increased activity of nuclear factor-kappa B participates in cardiovascular remodeling induced by chronic inhibition of nitric oxide synthesis in rats
Article
关键词: MONOCYTE CHEMOATTRACTANT PROTEIN-1;    LONG-TERM BLOCKADE;    CONVERTING ENZYME-INHIBITION;    CHEMOTACTIC PROTEIN-1;    ENDOTHELIAL-CELLS;    GENE-THERAPY;    EXPRESSION;    TRANSCRIPTION;    DISEASE;    ATHEROSCLEROSIS;   
DOI  :  10.1161/01.CIR.102.7.806
来源: SCIE
【 摘 要 】

Background-Chronic inhibition of endothelial nitric oxide (NO) synthesis by the administration of N-omega-nitro-L-arginine methyl ester (L-NAME) to rats induces early vascular inflammatory changes [monocyte infiltration into coronary vessels, nuclear factor-kappa B (NF-kappa B) activation, and monocyte chemoattractant protein-1 expression] as well as subsequent arteriosclerosis (medial thickening and perivascular fibrosis) and cardiac fibrosis. However, no direct evidence for the importance of NF-kappa B in this process is known. Methods and Results-We examined the effect of a cis element decoy strategy to address the functional importance of NF-kappa B in the pathogenesis of cardiovascular remodeling. We found here that in vivo transfection of cis element decoy oligodeoxynucleotides against NF-kappa B to hearts prevented the L-NAME-induced early inflammation and subsequent coronary vascular medial thickening. In contrast, NF-kappa B decoy oligodeoxynucleotide transfection did not decrease the development of fibrosis, the expression of transforming growth factor-beta(1) mRNA, or systolic pressure overload induced by L-NAME administration. Conclusions-The NF-kappa B system participates importantly in the development of early vascular inflammation and subsequent medial thickening but not in fibrogenesis in this model. The present study may provide a new aspect of how endothelium-derived NO contributes to anti-inflammatory and/or antiarteriosclerotic properties of the vascular endothelium in vivo.

【 授权许可】

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