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4,4-二氨基二苯砜抑制非吞噬性人二倍体成纤维细胞中 ROS 的生成。

Suppression of ROS generation by 4,4-diaminodiphenylsulfone in non-phagocytic human diploid fibroblasts.

机构信息

Department of Biochemistry and Molecular Biology, Aging and Apoptosis Research Center, Seoul National University College of Medicine, Seoul 110-799, Korea.

出版信息

Exp Mol Med. 2010 Mar 31;42(3):223-32. doi: 10.3858/emm.2010.42.3.024.

Abstract

The action mode of 4,4-diaminodiphenylsulfone (DDS) is still under debate, although it has long been used in treatment of several dermatologic diseases including Hansens disease. In this study, we tested the effect of DDS as an antioxidant on paraquat-induced oxidative stress in non-phagocytic human diploid fibroblasts (HDFs). Overall, preincubation of HDFs with DDS prevented the oxidative stress and the resulting cytotoxic damages caused by paraquat in these cells. The specific effects of DDS in paraquat-treated HDFs are summarized as follows: a) reducing the expression of NADPH oxidase 4 (NOX4) by inhibiting paraquat-induced activation of PKC; b) inhibiting paraquat-induced decreases in mitochondrial complex protein levels as well as in membrane potentials; c) consequently, inhibiting the generation of cytosolic and mitochondrial superoxide anions. Taken together, these findings suggest that DDS would suppress the radical generation in non-phagocytic HDFs during oxidative stress, and that DDS might have the extended potential to be used further in prevention of other oxidative stress-related pathologies.

摘要

尽管 4,4-二氨基二苯砜(DDS)已被长期用于治疗汉森病等多种皮肤科疾病,但它的作用模式仍存在争议。在这项研究中,我们测试了 DDS 作为抗氧化剂对百草枯诱导的非吞噬性人二倍体成纤维细胞(HDF)氧化应激的影响。总的来说,DDS 预处理可预防百草枯引起的氧化应激和由此导致的细胞毒性损伤。DDS 在百草枯处理的 HDF 中的具体作用总结如下:a)通过抑制百草枯诱导的 PKC 激活来减少 NADPH 氧化酶 4(NOX4)的表达;b)抑制百草枯诱导的线粒体复合物蛋白水平和膜电位降低;c)从而抑制胞质和线粒体超氧阴离子的产生。综上所述,这些发现表明,DDS 可抑制氧化应激过程中非吞噬性 HDF 中的自由基生成,并且 DDS 可能具有进一步用于预防其他氧化应激相关疾病的扩展潜力。

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