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Pentoxifylline inhibits the synthesis and IFN-γ-inducing activity of IL-18

机译:己酮可可碱抑制IL-18的合成和IFN-γ诱导活性

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摘要

The effect of phosphodiesterase-inhibiting anti-inflammatory drug pentoxifylline (PTX) on LPS-induced IL-18 synthesis and IL-18-mediated IFN-γ-induction were investigated. In a dose-dependent manner PTX inhibited production of IL-18 in LPS-treated cultures of murine spleen cells and bone marrow-derived macrophages. Similarly, PTX treatment significantly reduced blood IL-18 levels and expression of spleen IL-18 mRNA in LPS-challenged mice. The inhibitory effect of PTX was specific for IL-18, since LPS-induced IL-12 p40 release was not suppressed either in splenocyte cultures or blood of LPS-injected animals. Synergistic induction of IFN-γ by combined IL-12/IL-18 treatment was also inhibited by PTX in vitro and in vivo. Experiments with IL-12 pretreatment of splenocytes, followed by IL-18 stimulation, revealed that PTX suppressed both IL-12 and IL-18 signals responsible for IFN-γ induction. These results suggest that interference with IL-18 synthesis and IFN-γ-inducing activity might contribute to anti-inflammatory actions of PTX.
机译:研究了磷酸二酯酶抑制消炎药己酮可可碱(PTX)对LPS诱导的IL-18合成和IL-18介导的IFN-γ诱导的影响。 PTX以剂量依赖性方式抑制小鼠脾脏细胞和骨髓源性巨噬细胞经LPS处理的培养物中IL-18的产生。同样,PTX处理可显着降低LPS攻击小鼠的血液IL-18水平和脾脏IL-18 mRNA表达。 PTX的抑制作用对IL-18具有特异性,因为LPS诱导的IL-12 p40释放在脾细胞培养物中或LPS注射动物的血液中均不受抑制。通过IL-12 / IL-18联合治疗对IFN-γ的协同诱导在体外和体内也被PTX抑制。用IL-12预处理脾细胞,然后进行IL-18刺激的实验表明,PTX抑制了负责诱导IFN-γ的IL-12和IL-18信号。这些结果表明,对IL-18合成和IFN-γ诱导活性的干扰可能有助于PTX的抗炎作用。

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