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首页> 外文期刊>Pfluegers Archiv: European Journal of Physiology >Prostaglandin D(2) and J (2)-series (PGJ (2), Delta (12)-PGJ (2)) prostaglandins stimulate IL-6 and MCP-1, but inhibit leptin, expression and secretion by 3T3-L1 adipocytes.
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Prostaglandin D(2) and J (2)-series (PGJ (2), Delta (12)-PGJ (2)) prostaglandins stimulate IL-6 and MCP-1, but inhibit leptin, expression and secretion by 3T3-L1 adipocytes.

机译:前列腺素D(2)和J(2)系列(PGJ(2),Delta(12)-PGJ(2))前列腺素刺激IL-6和MCP-1,但抑制瘦素,3T3-L1脂肪细胞的表达和分泌。

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Prostaglandin D(2) and its derivatives PGJ(2) and Delta(12)-PGJ(2) strongly stimulate the synthesis and secretion by white adipocytes of the neurotrophin NGF. Here we have explored whether PGD(2) and the J(2)-series prostaglandins have pervasive effects on adipokine production. The influence of these prostaglandins on the production of the adipocyte hormones leptin and adiponectin, and the inflammatory factors IL-6 and monocyte chemoattractant protein 1 (MCP-1), were examined in 3T3-L1 adipocytes. PGD(2) induced a reduction in adiponectin and leptin mRNA, and the secretion of these adipokines was also inhibited, the effect being greater with leptin (up to 10-fold) than with adiponectin (twofold). In contrast, PGD(2) induced a marked stimulation of IL-6 and MCP-1 expression; with IL-6, this was rapid, the mRNA level increasing by >50-fold by 1 h. The rise in mRNA was accompanied by an increase in IL-6 and MCP-1 release (up to 100- and 6.5-fold, respectively). The effects of PGD(2) were generally mirrored by PGJ(2) and Delta(12)-PGJ(2); Delta(12)-PGJ(2) was a particularly strong stimulator of IL-6 production. These results indicate that PGD(2) and the J(2)-series prostaglandins PGJ(2) and Delta(12)-PGJ(2) can have major effects on the synthesis and release of key adipokines. Such effects could be important in the inflammatory response in adipose tissue.
机译:前列腺素D(2)及其衍生物PGJ(2)和Delta(12)-PGJ(2)强烈刺激神经营养蛋白NGF的白色脂肪细胞合成和分泌。在这里,我们探讨了PGD(2)和J(2)系列前列腺素是否对脂肪因子的产生具有普遍的影响。在3T3-L1脂肪细胞中检查了这些前列腺素对脂肪细胞激素瘦素和脂联素的产生以及炎症因子IL-6和单核细胞趋化蛋白1(MCP-1)的影响。 PGD​​(2)诱导脂联素和瘦素mRNA的减少,并且这些脂联因子的分泌也受到抑制,瘦素的作用(高达10倍)比脂连蛋白(两倍)更大。相比之下,PGD(2)诱导了IL-6和MCP-1表达的明显刺激。对于IL-6,这是快速的,在1小时内,mRNA水平增加了> 50倍。 mRNA的增加伴随着IL-6和MCP-1释放的增加(分别高达100倍和6.5倍)。 PGD​​(2)的效果通常由PGJ(2)和Delta(12)-PGJ(2)反映出来; Delta(12)-PGJ(2)是IL-6生产的特别强大的刺激剂。这些结果表明,PGD(2)和J(2)系列前列腺素PGJ(2)和Delta(12)-PGJ(2)可以对关键脂肪因子的合成和释放产生重大影响。这种作用在脂肪组织的炎症反应中可能很重要。

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