Muir K W
University Department of Neurology, Institute of Neurological Sciences, Southern General Hospital, Glasgow, Scotland, UK.
CNS Drugs. 2001;15(12):921-30. doi: 10.2165/00023210-200115120-00002.
Magnesium exhibits a range of neuronal and vascular actions that may ameliorate ischaemic CNS insults, including stroke. Significant neuroprotection with magnesium has been observed in different models of focal cerebral ischaemia in many laboratories, with infarct volume reductions between 25 and 61%. Maximal neuroprotection is evident at readily attainable serum concentrations, and neuroprotection is still seen when administration is delayed up to 6 hours after onset of ischaemia. Clinical use of magnesium in pre-eclampsia and acute myocardial infarction confirms its safety and tolerability. Five small trials in acute stroke have reported reduced odds of death or dependence with administration of magnesium, but confidence intervals are wide, and definitive data from ongoing large trials are awaited.
镁具有一系列神经和血管作用,可能改善包括中风在内的缺血性中枢神经系统损伤。许多实验室在不同的局灶性脑缺血模型中均观察到镁具有显著的神经保护作用,梗死体积减少了25%至61%。在易于达到的血清浓度下即可显现出最大程度的神经保护作用,并且在缺血发作后延迟给药长达6小时仍可见神经保护作用。镁在子痫前期和急性心肌梗死中的临床应用证实了其安全性和耐受性。五项急性中风的小型试验报告称,使用镁可降低死亡或依赖的几率,但置信区间较宽,仍在等待正在进行的大型试验得出的确切数据。