Program in Clinical and Experimental Therapeutics, University of Georgia College of Pharmacy, HM 1200, 1120 15th St., Augusta, GA 30912, USA. Charlie Norwood VA Medical Center, Augusta, GA, USA. Department of Neurology, Georgia Health Sciences University, Augusta, GA, USA.
Transl Stroke Res. 2011 Jun 1;2(2):202-8. doi: 10.1007/s12975-011-0072-6.
Minocycline, a tetracycline antibiotic, has shown anti-inflammatory, anti-apoptotic, and neuroprotective effects in many models of cerebral ischemia and neurodegenerative disease. Its high penetration of the blood-brain barrier, good safety profile, and delayed therapeutic window make it an ideal candidate for use in stroke. In animal models, minocycline reduced infarct size and improved neurologic outcome when administered acutely, with similar neuroprotective benefits seen following delayed administration. To date, two early phase clinical trials have shown minocycline to be safe and potentially effective in acute ischemic stroke, alone or in combination with tissue plasminogen activator. A large efficacy clinical trial is now needed to confirm previous studies, allow for subgroup analysis, and pinpoint the potential place for minocycline in acute stroke therapy.
米诺环素是一种四环素类抗生素,在许多脑缺血和神经退行性疾病模型中表现出抗炎、抗细胞凋亡和神经保护作用。其对血脑屏障的高穿透性、良好的安全性和延迟的治疗窗口使其成为治疗中风的理想候选药物。在动物模型中,米诺环素在急性给药时可减少梗死面积并改善神经功能结局,延迟给药也可观察到类似的神经保护作用。迄今为止,两项早期临床试验表明,米诺环素单独或联合组织型纤溶酶原激活剂用于急性缺血性中风是安全且可能有效的。目前需要进行一项大型疗效临床试验来证实先前的研究结果,进行亚组分析,并确定米诺环素在急性中风治疗中的潜在地位。