Samardzic T, Jankovic V, Stosic-Grujicic S, Popadic D, Trajkovic V
Institute for Biological Research Sinisa Stankovic, Belgrade, Yugoslavia.
Clin Exp Immunol. 2001 May;124(2):274-81. doi: 10.1046/j.1365-2249.2001.01546.x.
The effect of phosphodiesterase-inhibiting anti-inflammatory drug pentoxifylline (PTX) on LPS-induced IL-18 synthesis and IL-18-mediated IFN-gamma-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-gamma 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-gamma induction. These results suggest that interference with IL-18 synthesis and IFN-gamma-inducing activity might contribute to anti-inflammatory actions of PTX.
研究了磷酸二酯酶抑制性抗炎药物己酮可可碱(PTX)对脂多糖(LPS)诱导的白细胞介素-18(IL-18)合成及IL-18介导的γ干扰素(IFN-γ)诱导的影响。PTX以剂量依赖方式抑制LPS处理的小鼠脾细胞和骨髓来源巨噬细胞培养物中IL-18的产生。同样,PTX处理显著降低了LPS攻击小鼠的血液IL-18水平及脾脏IL-18 mRNA的表达。PTX的抑制作用对IL-18具有特异性,因为在脾细胞培养物或LPS注射动物的血液中,LPS诱导的IL-12 p40释放均未受到抑制。PTX在体外和体内也抑制了IL-12/IL-18联合处理对IFN-γ的协同诱导。对脾细胞进行IL-12预处理后再用IL-18刺激的实验表明,PTX抑制了负责IFN-γ诱导的IL-12和IL-18信号。这些结果提示,干扰IL-18合成及IFN-γ诱导活性可能有助于PTX的抗炎作用。