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氯法齐明诱导巨噬细胞凋亡的活性。

Apoptosis-inducing activity of clofazimine in macrophages.

机构信息

Leprosy Research Center, National Institute of Infectious Diseases, 4-2-1, Aoba-cho, Higashimurayama-shi, Tokyo 189-0002, Japan.

出版信息

Antimicrob Agents Chemother. 2011 Sep;55(9):4000-5. doi: 10.1128/AAC.00434-11. Epub 2011 Jun 20.

Abstract

Clofazimine is a riminophenazine compound which has been used for the treatment of leprosy since the 1960s. Although the drug is effective in the management of leprosy reactions because of its anti-inflammatory activity, the mechanism leading to the cessation of inflammation is not well understood. In the present study, it was shown that clofazimine exhibits apoptosis-inducing activity in macrophages. When human monocyte-derived macrophages were cultured in vitro in the presence of clofazimine, the cells exhibited a marked decrease in metabolic activity and showed shrinkage in cell size, indicating cell death. Nuclear condensation and fragmentation were also observed by Giemsa and Hoechst 33248 stains. The endonuclease inhibitor ZnCl(2) inhibited the clofazimine-induced cell death. Significant enhancement of caspase-3 activity was observed in clofazimine-treated macrophages and THP-1 cells. Collectively, these results suggest the apoptosis-inducing activity of clofazimine in macrophages, which may also be responsible for the antibacterial properties of clofazimine.

摘要

氯法齐明是一种苯并二氮嗪化合物,自 20 世纪 60 年代以来一直用于治疗麻风病。虽然该药物具有抗炎活性,因此在麻风病反应的治疗中非常有效,但导致炎症停止的机制尚不清楚。在本研究中,表明氯法齐明在巨噬细胞中表现出诱导细胞凋亡的活性。当人单核细胞衍生的巨噬细胞在存在氯法齐明的情况下在体外培养时,细胞的代谢活性明显下降,并且细胞体积缩小,表明细胞死亡。通过 Giemsa 和 Hoechst 33248 染色也观察到核浓缩和碎裂。核酸内切酶抑制剂 ZnCl2 抑制氯法齐明诱导的细胞死亡。在氯法齐明处理的巨噬细胞和 THP-1 细胞中观察到 caspase-3 活性显著增强。总的来说,这些结果表明氯法齐明在巨噬细胞中具有诱导细胞凋亡的活性,这也可能是氯法齐明具有抗菌特性的原因。

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