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首页> 外文期刊>Journal of Neuroscience Research >Retinoic acid enhances prostaglandin E2 production through increased expression of cyclooxygenase-2 and microsomal prostaglandin E synthase-1 in rat brain microglia.
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Retinoic acid enhances prostaglandin E2 production through increased expression of cyclooxygenase-2 and microsomal prostaglandin E synthase-1 in rat brain microglia.

机译:维甲酸通过增加大鼠脑小胶质细胞中环氧合酶2和微粒体前列腺素E合酶1的表达来增强前列腺素E2的产生。

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摘要

Retinoic acid (RA) is a well-known antiinflammatory agent. In this study, we show that RA has a dual effect on cyclooxygenase-2 (COX-2) expression in inflammatory activated microglia, the resident brain macrophages. After treatment of microglia with LPS or thrombin, COX-2 expression was induced in two phases, specifically, an initial increase at about 12 hr after stimulation followed by a decrease, and another increase at about 48-72 hr. However, PGE(2) and 15d-PGJ(2) were detected at about 12 hr, and the levels continuously increased thereafter. Interestingly, all-trans retinoic acid (ATRA) suppressed the expression of early-phase COX-2 but augmented late-phase COX-2 and inhibited iNOS in the whole time sequence. ATRA enhanced PGE(2) production but had little effect on 15d-PGJ(2). Moreover, ATRA selectively up-regulated the expression of a PGE(2) synthase, mPGES-1, but had little effect on the PGD(2) synthase, H-PGDS. The results collectively suggest that ATRA modulates microglial responses to inflammatory stimulators, particularly at the late phase, via enhancement of COX-2 expression and PGE(2) production.
机译:维甲酸(RA)是众所周知的抗炎药。在这项研究中,我们显示RA对炎症激活的小胶质细胞(常驻脑巨噬细胞)中的环氧合酶2(COX-2)表达具有双重作用。用LPS或凝血酶处理小胶质细胞后,COX-2表达在两个阶段被诱导,特别是在刺激后约12小时开始增加,然后减少,在约48-72小时又增加。但是,在大约12小时检测到PGE(2)和15d-PGJ(2),此后其水平持续增加。有趣的是,全反式维甲酸(ATRA)在整个时间序列中均抑制了早期COX-2的表达,但增加了晚期COX-2的表达并抑制了iNOS。 ATRA增强了PGE(2)的产量,但对15d-PGJ(2)的影响很小。此外,ATRA选择性上调PGE(2)合酶,mPGES-1的表达,但对PGD(2)合酶,H-PGDS的影响很小。这些结果共同表明,ATRA通过增强COX-2表达和PGE(2)的产生来调节对炎症刺激物的小胶质细胞应答,特别是在晚期。

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