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首页> 外文期刊>Biochimica et Biophysica Acta. General Subjects >Prostaglandin E_2 production and induction of prostaglandin endoperoxide synthase-2 is inhibited in a murine macrophage-like cell line, RAW 264.7, by Mallotus japonicus phoroglucinol derivatives
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Prostaglandin E_2 production and induction of prostaglandin endoperoxide synthase-2 is inhibited in a murine macrophage-like cell line, RAW 264.7, by Mallotus japonicus phoroglucinol derivatives

机译:在小鼠巨噬细胞样细胞系RAW 264.7中,Mallotus japonicus phorluclucinol衍生物可抑制前列腺素E_2的产生和前列腺素内过氧化物合酶2的诱导。

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An aqueous acetone extract obtained from the pericarps of Mallotus japonicus (MJE) was observed to inhibit prostaglandin (PG) E_2 production in a lipopolysaccharide (LPS)-activated murine macrophage-like cell line, RAW 264.7. Six phloroglucinol derivatives isolated from MJE exhibited inhibitory activity against PGE_2 production. Among these phloroglucinol derivatives, isomallotochromanol showed the strongest inhibitor activity, with an IC_(50) of 1.0 μM. MJE and its phloroglucinol derivatives did not effect the enzyme activity of either prostaglandin endoperoxide synthase (PGHS)-1 or PGHS-2. However, induction of PGHS-2 in LPS-activated macrophages was inhibited by MJE and its phloroglucinol derivatives, whereas the level of PGHS-1 protein was not affected. Moreover, RT-PCR analysis showed that MJE and its phloroglucinol derivatives significantly suppressed PGHS-2 mRNA expression. Therefore, the observed inhibition of PGHS-2 induction by MJE and its phloroglucinol derivatives was likely due to a suppression of PGHS-2 mRNA expression. These results suggest that MJE and its phloroglucinol derivatives have the pharmacological ability to suppress PGE_2 production by activated macrophages.
机译:在脂多糖(LPS)激活的鼠巨噬细胞样细胞系RAW 264.7中,观察到从Mallotus japonicus(MJE)的果皮中获得的丙酮水提取物抑制前列腺素(PG)E_2的产生。从MJE中分离出的六种间苯三酚衍生物对PGE_2的产生具有抑制活性。在这些间苯三酚衍生物中,异麦芽酚苯甲醇显示出最强的抑制剂活性,IC_(50)为1.0μM。 MJE及其间苯三酚衍生物不会影响前列腺素内过氧化物合酶(PGHS)-1或PGHS-2的酶活性。但是,MJE及其间苯三酚衍生物可抑制LPS活化的巨噬细胞中PGHS-2的诱导,而PGHS-1蛋白的水平不受影响。此外,RT-PCR分析显示MJE及其间苯三酚衍生物可显着抑制PGHS-2 mRNA的表达。因此,观察到的MJE及其间苯三酚衍生物对PGHS-2诱导的抑制作用可能是由于PGHS-2 mRNA表达的抑制。这些结果表明,MJE及其间苯三酚衍生物具有抑制活化巨噬细胞产生PGE_2的药理能力。

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