Wang Jintao, Wang Hui, Guo Chiao, Luo Wei, Lawler Alyssa, Reddy Aswin, Wang Julia, Sun Eddy B, Eitzman Daniel T
University of Michigan, Department of Internal Medicine, Cardiovascular Research Center, Ann Arbor, Michigan, United States of America.
PLoS One. 2014 Feb 27;9(2):e90146. doi: 10.1371/journal.pone.0090146. eCollection 2014.
Mebendazole is an antihelminthic drug that exerts its effects via interference with microtubule function in parasites. To determine the utility of mebendazole as a potential treatment for vascular diseases involving proliferation of vascular smooth muscle cells, the effects of mebendazole on vascular smooth muscle cell proliferation were tested in vitro and in a mouse model of arterial injury. In vitro, mebendazole inhibited proliferation and migration of murine vascular smooth muscle cells and this was associated with altered intracellular microtubule organization. To determine in vivo effects of mebendazole following vascular injury, femoral arterial wire injury was induced in wild-type mice treated with either mebendazole or placebo control. Compared with placebo-treated mice, mebendazole-treated mice formed less neointima at the site of injury. Mebendazole is effective at inhibiting vascular smooth muscle cell proliferation and migration, and neointimal formation following arterial injury in mice.
甲苯咪唑是一种抗蠕虫药物,它通过干扰寄生虫的微管功能发挥作用。为了确定甲苯咪唑作为涉及血管平滑肌细胞增殖的血管疾病潜在治疗方法的效用,在体外和动脉损伤小鼠模型中测试了甲苯咪唑对血管平滑肌细胞增殖的影响。在体外,甲苯咪唑抑制小鼠血管平滑肌细胞的增殖和迁移,这与细胞内微管组织的改变有关。为了确定血管损伤后甲苯咪唑的体内作用,在用甲苯咪唑或安慰剂对照治疗的野生型小鼠中诱导股动脉钢丝损伤。与安慰剂治疗的小鼠相比,甲苯咪唑治疗的小鼠在损伤部位形成的新内膜较少。甲苯咪唑在抑制小鼠动脉损伤后的血管平滑肌细胞增殖、迁移和新内膜形成方面是有效的。