Modulation of macrophage activation by prostaglandins

被引:5
作者
Sautebin, L
Carnuccio, R
DAcquisto, F
DiRosa, M
机构
[1] Department of Experimental Pharmacology, University of Naples “Federico II”, 80131 Naples
关键词
cAMP; macrophages; nitric oxide; phosphodiesterase inhibitor; prostaglandins; tumour necrosis factor;
D O I
10.1155/S0962935196000026
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The effect of prostaglandin E(2), iloprost and cAMP on both nitric oxide and tumour necrosis factor-alpha release in J774 macrophages has been studied. Both prostaglandin E(2) and iloprost inhibited, in a concentration-dependent fashion the lipopolysaccharide-induced generation of nitric oxide and tumour necrosis factor-alpha. The inhibitory effect of these prostanoids seems to be mediated by an increase of the second messenger cAMP since it was mimicked by dibutyryl cAMP and potentiated by the selective type IV phosphodiesterase inhibitor RO-20-1724. Our results suggest that the inhibition of nitric oxide release by prostaglandin E(2) and iloprost in lipopolysaccharide-activated J774 macrophages may be secondary to the inhibition of tumour necrosis factor-alpha generation, which in turn is likely to be mediated by cAMP.
引用
收藏
页码:14 / 17
页数:4
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