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

机译:非吞噬人类二倍体成纤维细胞中4,4'-二氨基二苯砜抑制ROS生成

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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 Hansen's 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.
机译:尽管4,4'-二氨基二苯砜(DDS)的作用方式长期以来一直用于治疗包括汉森氏病在内的多种皮肤病,但仍在争论中。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类二倍体成纤维细胞(HDFs)的氧化应激的作用。总体而言,HDF与DDS的预孵育可防止氧化应激以及由百草枯引起的细胞毒性损害。 DDS在百草枯处理的HDF中的特定作用概述如下:a)通过抑制百草枯诱导的PKC活化来降低NADPH氧化酶4(NOX4)的表达; b)抑制百草枯引起的线粒体复合蛋白水平以及膜电位下降; c)因此,抑制了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将抑制非吞噬性HDF在氧化应激期间的自由基生成,并且DDS可能具有扩展的潜力,可进一步用于预防其他与氧化应激相关的病理。

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