首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Prostaglandin E2 inhibits and indomethacin and aspirin enhance A23187-stimulated leukotriene B4 synthesis by rat peritoneal macrophages.
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Prostaglandin E2 inhibits and indomethacin and aspirin enhance A23187-stimulated leukotriene B4 synthesis by rat peritoneal macrophages.

机译:前列腺素E2抑制并消炎痛和阿司匹林增强A23187刺激的大鼠腹膜巨噬细胞合成白三烯B4。

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摘要

1. The calcium ionophore, A23187, stimulated leukotriene B4 (LTB4), thromboxane B2 (TxB2) and prostaglandin E2 (PGE2) synthesis by 4 day carrageenin-elicited rat peritoneal macrophages. 2. At concentrations of 2 x 10(-7)-2 x 10(-5) M indomethacin and aspirin enhanced A23187-stimulated LTB4 synthesis and inhibited PGE2 and TXB2 formation. 3. PGE2 inhibited A23187-stimulated LTB4 and TXB2 formation as well as the augmentation of LTB4 release caused by aspirin and indomethacin. However, PGE2 was ineffective when the cells were challenged with arachidonic acid (AA). 4. Dibutyryl adenosine 3':5'-cyclic monophosphate (db-cyclic AMP) partially inhibited A23187-stimulated LTB4 production. 5. Our results suggest that PGE2 inhibits macrophage LTB4 synthesis by limiting the availability of AA. Indomethacin and aspirin, possibly by removing the regulatory effect of PGE2, promote the synthesis of the pro-inflammatory LTB4.
机译:1.钙离子载体A23187通过角叉菜胶诱导的大鼠腹膜巨噬细胞刺激白三烯B4(LTB4),血栓烷B2(TxB2)和前列腺素E2(PGE2)的合成。 2.在2 x 10(-7)-2 x 10(-5)M的浓度下,吲哚美辛和阿司匹林增强A23187刺激的LTB4合成,并抑制PGE2和TXB2的形成。 3. PGE2抑制了A23187刺激的LTB4和TXB2的形成,以及阿司匹林和消炎痛引起的LTB4释放的增加。但是,当用花生四烯酸(AA)攻击细胞时,PGE2无效。 4.二丁酰腺苷3':5'-环一磷酸酯(db-环AMP)部分抑制A23187刺激的LTB4产生。 5.我们的结果表明,PGE2通过限制AA的可用性抑制巨噬细胞LTB4的合成。消炎痛和阿司匹林可能通过消除PGE2的调节作用来促进促炎性LTB4的合成。

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