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泰利霉素在体外刺激的小鼠细胞中抑制促炎介质的产生和核因子κB的激活。

Telithromycin inhibits the production of proinflammatory mediators and the activation of NF-kappaB in in vitro-stimulated murine cells.

作者信息

Leiva Magdalena, Ruiz-Bravo Alfonso, Moreno Encarnación, Jiménez-Valera Maria

机构信息

Department of Microbiology, Faculty of Pharmacy, University of Granada, Granada, Spain.

出版信息

FEMS Immunol Med Microbiol. 2008 Aug;53(3):343-50. doi: 10.1111/j.1574-695X.2008.00424.x. Epub 2008 Jun 28.

Abstract

Telithromycin is a ketolide antibiotic with anti-inflammatory properties. To investigate the mechanisms of these effects, we examined the in vitro immunomodulatory activity of telithromycin on murine splenocytes and the murine macrophage cell line RAW 264.7. Spleen cells from BALB/c-untreated mice and RAW 264.7 macrophages were cultured in the presence of telithromycin. Proliferation and apoptosis (colorimetric assay), and cytokine production (enzyme immunoassay) of spleen cells in response to lipopolysaccharide and concanavalin A (Con A), and nitric oxide (NO) (colorimetric assay) and cytokine production by lipopolysaccharide-stimulated RAW 264.7 cells were determined. Telithromycin moderately enhanced lymphocyte proliferation in response to lipopolysaccharide and Con A, and enhanced apoptosis induced by camptothecin in mitogen-stimulated splenocytes. Con A-induced IFN-gamma production was suppressed and lipopolysaccharide-induced IL-10 production was increased in spleen cell cultures with telithromycin. Lipopolysaccharide-induced secretion of NO and tumor necrosis factor-alpha (TNF-alpha) was suppressed by telithromycin in RAW 264.7 cultures. Lipopolysaccharide-induced activation of NF-kappaB transcription factor and TNF-alpha promoter in RAW 264.7 macrophages transitorily transfected with luciferase reporter constructs was also inhibited by the ketolide. The suppressive effect of telithromycin on NF-kappaB activation was confirmed by Western blot and enzyme immunoassay. These results suggest that telithromycin exerts anti-inflammatory activity mediated by the inhibition of activation of NF-kappaB.

摘要

泰利霉素是一种具有抗炎特性的酮内酯类抗生素。为了研究这些作用的机制,我们检测了泰利霉素对小鼠脾细胞和小鼠巨噬细胞系RAW 264.7的体外免疫调节活性。将来自未处理的BALB/c小鼠的脾细胞和RAW 264.7巨噬细胞在泰利霉素存在的情况下进行培养。测定脾细胞对脂多糖和伴刀豆球蛋白A(Con A)的增殖和凋亡(比色法)以及细胞因子产生(酶免疫测定),以及脂多糖刺激的RAW 264.7细胞产生的一氧化氮(NO)(比色法)和细胞因子。泰利霉素适度增强了脾细胞对脂多糖和Con A的淋巴细胞增殖,并增强了喜树碱在有丝分裂原刺激的脾细胞中诱导的凋亡。在含有泰利霉素的脾细胞培养物中,Con A诱导的γ干扰素产生受到抑制,脂多糖诱导的白细胞介素-10产生增加。在RAW 264.7培养物中,泰利霉素抑制了脂多糖诱导的NO和肿瘤坏死因子-α(TNF-α)的分泌。用荧光素酶报告构建体瞬时转染的RAW 264.7巨噬细胞中,脂多糖诱导的核因子-κB转录因子和TNF-α启动子的激活也受到该酮内酯的抑制。通过蛋白质免疫印迹法和酶免疫测定证实了泰利霉素对核因子-κB激活的抑制作用。这些结果表明,泰利霉素通过抑制核因子-κB的激活发挥抗炎活性。

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