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[抗生素对巨噬细胞白细胞介素-1产生的影响]

[Influence of antibiotics on the production of interleukin-1 by macrophages].

作者信息

Gillissen G, Melzer B

出版信息

Pathol Biol (Paris). 1985 Jun;33(5 Pt 2):521-4.

PMID:3911147
Abstract

Influence of cefoxitin and cefotaxime on interleukin-1 production (IL-1) by mice peritoneal resident macrophages activated by opsonized zymosan was investigated. Evaluation of the in vivo effect was done by examining macrophages of animals following intravenous administration of 30 mg/kg cefoxitin or cefotaxime. In vitro studies consisted in testing IL-1 production by macrophages in cell cultures in the presence of either antibiotic. In vivo IL-1 production was unchanged following cefoxitin treatment of cell donors, whereas a more than threefold increase was observed after administration of cefotaxime. In vitro, IL-1 production was enhanced by both antibiotics, but the pattern and extent of this effect diverged widely. Cefoxitin in a concentration of 300 micrograms/ml induced a threefold increase in IL-1 production. IL-1 production was increased tenfold and eightfold respectively by 150 and 300 micrograms/ml cefotaxime. When the concentration of either antibiotic was very high (400 micrograms/ml), the effect was significantly less important; a certain degree of inhibition was even observed with cefotaxime. Effects of cefoxitin and cefotaxime on IL-1 production and--as shown in previous studies--on prostaglandin E2 (PGE2) production and sensitivity of immunocompetent cells to PGE2 may be important factors in the mechanism of immunological side effects which result in a modulation of the course of experimental infection.

摘要

研究了头孢西丁和头孢噻肟对经调理酵母聚糖激活的小鼠腹腔常驻巨噬细胞产生白细胞介素-1(IL-1)的影响。通过检查静脉注射30mg/kg头孢西丁或头孢噻肟后动物的巨噬细胞来评估体内效应。体外研究包括在存在任一抗生素的情况下测试细胞培养物中巨噬细胞产生IL-1的情况。头孢西丁处理细胞供体后体内IL-1产生未改变,而注射头孢噻肟后观察到增加了三倍多。在体外,两种抗生素均增强了IL-1的产生,但这种效应的模式和程度差异很大。浓度为300μg/ml的头孢西丁使IL-1产生增加了三倍。150μg/ml和300μg/ml的头孢噻肟分别使IL-1产生增加了十倍和八倍。当任一抗生素的浓度非常高(400μg/ml)时,效应明显不那么重要;甚至观察到头孢噻肟有一定程度的抑制作用。头孢西丁和头孢噻肟对IL-1产生的影响以及——如先前研究所示——对前列腺素E2(PGE2)产生和免疫活性细胞对PGE2敏感性的影响可能是免疫副作用机制中的重要因素,这些副作用会导致实验性感染进程的调节。

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