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地塞米松对维甲酸诱导的大鼠嗜碱性白血病-1细胞中白三烯C4合成增强的抑制作用。

Inhibition by dexamethasone of retinoic acid-induced enhancement of leukotriene C4 synthesis in rat basophilic leukemia-1 cells.

作者信息

Hamasaki Y, Abe M, Matsumoto S, Ichimaru T, Kobayashi I, Tanaka E, Matsuo M, Hara N, Miyazaki S

机构信息

Department of Pediatrics, Saga Medical School, Japan.

出版信息

Am J Respir Cell Mol Biol. 1994 Jul;11(1):49-56. doi: 10.1165/ajrcmb.11.1.8018338.

Abstract

We investigated inhibitory actions of dexamethasone (DEX) on retinoic acid (RA)-induced enhancement of leukotriene C4 (LTC4) synthesis in rat basophilic leukemia-1 (RBL-1) cells. Cultured cells were preincubated with RA for 16 h with or without DEX, and generation of LTC4 was measured by high performance liquid chromatography in cell-free and intact cell systems. RA (0.1 microgram/ml) significantly potentiated calcium ionophore-stimulated production of LTC4 synthesis. DEX inhibited the RA-induced enhancement of LTC4 synthesis by up to approximately 95% in intact cells when stimulated with calcium ionophore. RA-induced LTC4 synthase activity, which was determined by enzyme assay, was also inhibited by DEX by 65% in a cell-free system. This discrepancy of inhibition between the intact and cell-free systems was due to a partial inhibition of phospholipase A2 activity by DEX in the intact cells. These results indicate that the production of LTC4 is predominantly regulated at a level of LTC4 synthase. The induction of new LTC4 synthase activity by RA and inhibition of the RA-induced activity by DEX are important regulatory mechanisms of LTC4 synthesis.

摘要

我们研究了地塞米松(DEX)对维甲酸(RA)诱导的大鼠嗜碱性白血病-1(RBL-1)细胞中白三烯C4(LTC4)合成增强的抑制作用。将培养的细胞在有或没有DEX的情况下与RA预孵育16小时,并通过高效液相色谱法在无细胞和完整细胞系统中测量LTC4的生成。RA(0.1微克/毫升)显著增强了钙离子载体刺激的LTC4合成。当用钙离子载体刺激时,DEX在完整细胞中抑制RA诱导的LTC4合成增强高达约95%。通过酶测定确定的RA诱导的LTC4合酶活性在无细胞系统中也被DEX抑制了65%。完整细胞和无细胞系统之间抑制作用的这种差异是由于DEX在完整细胞中对磷脂酶A2活性的部分抑制。这些结果表明,LTC4的产生主要在LTC4合酶水平受到调节。RA诱导新的LTC4合酶活性以及DEX对RA诱导活性的抑制是LTC4合成的重要调节机制。

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