新型抗炎药3-甲酰基氨基-7-甲基磺酰基氨基-6-苯氧基- 4h -1-苯并吡喃-4-酮(T-614)的药理研究。第四通讯:抑制白细胞介素-1和白细胞介素-6的产生。

K Tanaka, Y Aikawa, H Kawasaki, K Asaoka, T Inaba, C Yoshida
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引用次数: 37

摘要

在体外研究了新型抗炎化合物3-甲酰基氨基-7-甲基磺酰基氨基-6-苯氧基- 4h -1-苯并吡喃-4-on (T-614)对人单核细胞和人单核细胞系THP-1细胞产生白细胞介素-1 (IL-1)和/或白细胞介素-6 (IL-6)的影响。T-614以剂量依赖性的方式(0.3-30微克/毫升)抑制免疫反应性IL-1 β从脂多糖(LPS)刺激的细胞释放。T-614对THP-1细胞IL-6的释放有抑制作用,其IC50值分别为2.0和6.6微克/毫升。lps刺激的THP-1细胞的Northern blotting分析表明,T-614对IL-1 β产生的抑制作用是通过抑制IL-1 β mRNA的表达引起的。T-614对细胞因子产生的抑制可能为其抗炎活性的其他机制提供了重要的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pharmacological studies on 3-formylamino-7-methylsulfonylamino-6-phenoxy-4H-1-benzopyran-4-one (T-614), a novel antiinflammatory agent. 4th communication: inhibitory effect on the production of interleukin-1 and interleukin-6.

In vitro effects of 3-formylamino-7-methylsulfonylamino-6-phenoxy-4H-1-benzopyran-4-on e (T-614), a novel antiinflammatory compound, on the production of interleukin-1 (IL-1) and/or interleukin-6 (IL-6) by human monocytes and the THP-1 cells of a human monocytic cell line, were examined. T-614 inhibited the release of immunoreactive IL-1 beta from these cells stimulated with lipopolysaccharides (LPS) in a dose-dependent manner (0.3-30 micrograms/ml). The release of IL-6 from THP-1 cells, as determined by the assays for its hepatocyte-stimulating activities and immunoreactivities, was inhibited by T-614 with the IC50 values of 2.0 and 6.6 micrograms/ml, respectively. Northern blotting analysis using LPS-stimulated THP-1 cells indicated that the inhibitory effect of T-614 on IL-1 beta production is caused by the suppression of IL-1 beta mRNA expression. The inhibition of cytokine production by T-614 may provide an important insight into the additional mechanisms contributing to its antiinflammatory activities.

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