Yu Guolong, Hess David C, Borlongan Cesario V
Research and Affiliations Service Line, VAMC Augusta, GA 30912, USA.
Brain Res. 2004 Aug 20;1018(1):32-7. doi: 10.1016/j.brainres.2004.05.056.
We investigated the neuroprotective effects of immunosuppressant cyclosporine-A (CsA) and the anti-inflammatory methylprednisolone (MP) in a stroke model. Adult Sprague-Dawley rats underwent middle cerebral artery (MCA) occlusion then were randomly treated with either: low dose CsA, MP, low dose CsA plus MP, high dose CsA, or vehicle. Ischemic animals that received low dose CsA, MP or vehicle displayed profound motor and neurological impairments at days 1-3 after stroke. In contrast, ischemic animals that received high dose CsA exhibited near normal motor and neurological functions throughout the test period. Of note, ischemic animals that received low dose CsA plus MP showed significantly less motor and neurological deficits at day 1, but thereafter displayed behavioral impairments. Histological analysis at 3 days post-stroke revealed that only those ischemic animals treated with high dose CsA had significantly reduced cerebral infarcts. This study is the first report to demonstrate partial and transient neuroprotection against stroke by low dose CsA when combined with MP.
我们在中风模型中研究了免疫抑制剂环孢素A(CsA)和抗炎药物甲泼尼龙(MP)的神经保护作用。成年Sprague-Dawley大鼠接受大脑中动脉(MCA)闭塞手术,然后随机接受以下治疗:低剂量CsA、MP、低剂量CsA加MP、高剂量CsA或赋形剂。接受低剂量CsA、MP或赋形剂的缺血动物在中风后第1至3天表现出严重的运动和神经功能障碍。相比之下,接受高剂量CsA的缺血动物在整个测试期间表现出接近正常的运动和神经功能。值得注意的是,接受低剂量CsA加MP的缺血动物在第1天显示出明显较少的运动和神经功能缺损,但此后出现行为障碍。中风后3天的组织学分析表明,只有那些接受高剂量CsA治疗的缺血动物脑梗死明显减少。本研究是首次报道低剂量CsA与MP联合使用时对中风具有部分和短暂的神经保护作用。