Liu Na, Zhuang Shougang
Department of Medicine, Rhode Island Hospital and Brown University School of Medicine, Providence, RI 02903, USA.
Curr Clin Pharmacol. 2011 May;6(2):137-42. doi: 10.2174/157488411796151174.
Suramin is a polysulfonated naphthylurea, which was originally synthesized and designed as a treatment for trypanosomiasis and selected malignancies and metastatic diseases. Increasing evidence indicates that suramin is also effective in interfering with many other pathophysiological processes in animal models. For example, suramin can enhance renal regeneration after ischemia/reperfusion injury, attenuate liver damage following CD95 stimulation and endotoxic shock, reduce brain injury induced by ischemia, and suppress myocardial inflammation. Further, suramin has an anti-fibrotic effect in liver and muscle. Mechanistic studies show that suramin inhibits apoptosis, suppresses expression of proinflammatory cytokines, inactivates myofibroblasts and stimulates proliferation of renal epithelial cells. This review highlights the novel actions of suramin in a variety of tissues and organs.
苏拉明是一种多磺酸化萘脲,最初合成并设计用于治疗锥虫病以及特定的恶性肿瘤和转移性疾病。越来越多的证据表明,苏拉明在动物模型中对干扰许多其他病理生理过程也有效。例如,苏拉明可增强缺血/再灌注损伤后的肾脏再生,减轻CD95刺激和内毒素休克后的肝损伤,减少缺血诱导的脑损伤,并抑制心肌炎症。此外,苏拉明在肝脏和肌肉中具有抗纤维化作用。机制研究表明,苏拉明可抑制细胞凋亡,抑制促炎细胞因子的表达,使肌成纤维细胞失活,并刺激肾上皮细胞增殖。本综述重点介绍了苏拉明在多种组织和器官中的新作用。