首页> 外文期刊>Prostaglandins, Leukotrienes, and Essential Fatty Acids >Macrolide antibiotics inhibit prostaglandin E(2) synthesis and mRNA expression of prostaglandin synthetic enzymes in human leukocytes.
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Macrolide antibiotics inhibit prostaglandin E(2) synthesis and mRNA expression of prostaglandin synthetic enzymes in human leukocytes.

机译:大环内酯类抗生素抑制人白细胞中前列腺素E(2)的合成和前列腺素合成酶的mRNA表达。

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摘要

We investigated the action of macrolide antibiotics, which are considered to have anti-inflammatory activity, on lipopolysaccharide (LPS)-stimulated prostaglandin (PG) E(2) synthesis and the expression of mRNAs for cytosolic phospholipase A(2) (cPLA(2)), cyclooxygenase (COX)-1, and COX-2 in human leukocytes. The production of LPS-stimulated PGE(2) was significantly increased in peripheral polymorphonuclear leukocytes (PMNLs) and in mononuclear leukocytes (MNLs). Amounts of mRNAs for COX-2 and cPLA(2), but not for COX-1, were enhanced by LPS in PMNLs and MNLs. The LPS-enhanced PGE(2) synthesis and the expression of cPLA(2) and COX-2 mRNAs were inhibited by clarithromycin, azithromycin and dexamethasone in PMNLs and MNLs. The mRNA expression of COX-1 in PMNLs was decreased by clarithromycin and azithromycin. Macrolide antibiotics inhibited PGE(2) synthesis in human leukocytes by suppressing cPLA(2), COX-1, and COX-2 mRNA expression. These data indicate one mechanism of macrolide anti-inflammatory activity.
机译:我们调查了被认为具有抗炎活性的大环内酯类抗生素对脂多糖(LPS)刺激的前列腺素(PG)E(2)合成以及胞质磷脂酶A(2)(cPLA(2)mRNA表达的作用)),人白细胞中的环氧合酶(COX)-1和COX-2。 LPS刺激的PGE(2)的产量在外周多形核白细胞(PMNLs)和单核白细胞(MNLs)中显着增加。在PMNL和MNL中,LPS增强了COX-2和cPLA(2)而不是COX-1的mRNA含量。 LPS增强的PGE(2)合成以及cPLA(2)和COX-2 mRNA的表达被克拉霉素,阿奇霉素和地塞米松在PMNL和MNL中抑制。克拉霉素和阿奇霉素使PMNLs中COX-1的mRNA表达降低。大环内酯类抗生素通过抑制cPLA(2),COX-1和COX-2 mRNA表达来抑制人白细胞中PGE(2)的合成。这些数据表明大环内酯类抗炎活性的一种机制。

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