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氨氯地平对人肺泡巨噬细胞源性细胞因子的抑制作用。

Suppression of human alveolar macrophage-derived cytokines by amiloride.

作者信息

Rolfe M W, Kunkel S L, Rowens B, Standiford T J, Cragoe E J, Strieter R M

机构信息

Department of Internal Medicine, University of Michigan Hospitals, Ann Arbor.

出版信息

Am J Respir Cell Mol Biol. 1992 Jun;6(6):576-82. doi: 10.1165/ajrcmb/6.6.576.

Abstract

Various human alveolar macrophage (AM)-derived cytokines in the lungs have been shown to be present under conditions of normal homeostasis as well as during the pathogenesis of inflammation. Although extensive investigation has demonstrated the induction of cytokines from AM, relatively little is known regarding endogenous and exogenous regulation of their production. Several pharmacologic agents, including corticosteroids, cyclooxygenase inhibitors, prostaglandins, and methyl-xanthines have been examined for their role in the modulation of mononuclear phagocyte-derived cytokines. In this study, we examine the role of amiloride for the regulation of AM-derived interleukin (IL)-8, tumor necrosis factor (TNF), IL-6, and IL-1 beta. Amiloride in concentrations of 10(-4) to 10(-6) M, concentrations capable of being achieved in the distal airways via nebulization, were shown to inhibit lipopolysaccharide-stimulated, AM-derived IL-8 and TNF in both a time- and dose-dependent fashion. In addition, 5-(N,N-hexamethylene) amiloride hydrochloride, an amiloride analogue with specific sodium channel antiport inhibition, resulted in a similar dose-dependent suppression of lipopolysaccharide-stimulated, AM-derived IL-8 production. Furthermore, the suppressive effect of amiloride appeared to be at the level of mRNA for IL-8, TNF, IL-1 beta, and IL-6, whereas steady-state levels of beta-actin mRNA remained unaltered. These findings would suggest that amiloride has a potentially important modulating influence for the regulation of AM-derived cytokines.

摘要

肺内多种源自人肺泡巨噬细胞(AM)的细胞因子已被证明在正常稳态条件下以及炎症发病过程中均有存在。尽管广泛的研究已证实AM可诱导细胞因子产生,但关于其产生的内源性和外源性调节相对知之甚少。包括皮质类固醇、环氧化酶抑制剂、前列腺素和甲基黄嘌呤在内的几种药物制剂已被研究其在调节单核吞噬细胞衍生细胞因子中的作用。在本研究中,我们研究了氨氯地平对AM衍生的白细胞介素(IL)-8、肿瘤坏死因子(TNF)、IL-6和IL-1β的调节作用。浓度为10⁻⁴至10⁻⁶ M的氨氯地平,通过雾化可在远端气道达到该浓度,结果显示其能以时间和剂量依赖性方式抑制脂多糖刺激的、AM衍生的IL-8和TNF。此外,5-(N,N-六亚甲基)盐酸氨氯地平,一种具有特异性钠通道反向转运抑制作用的氨氯地平类似物,对脂多糖刺激的、AM衍生的IL-8产生也有类似的剂量依赖性抑制作用。此外,氨氯地平的抑制作用似乎作用于IL-8、TNF、IL-1β和IL-6的mRNA水平,而β-肌动蛋白mRNA的稳态水平保持不变。这些发现表明氨氯地平对AM衍生细胞因子的调节可能具有重要的调节作用。

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