Department of Anesthesiology, Faculty of Medicine, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki, Japan.
Department of Anesthesiology, Tsukuba University Hospital Mito Clinical Education and Training Center, Mito Kyodo General Hospital, 3-2-7 Miya-Mach, Mito, Ibaraki, Japan.
Neurocrit Care. 2020 Aug;33(1):64-72. doi: 10.1007/s12028-019-00862-w.
Global ischemia due to cardiac arrest (CA) followed by cardiopulmonary resuscitation (CPR) causes significant neuronal damage in vulnerable areas in the brain. Currently, a majority of patients eventually die after successful CPR due to neurological injury. Statins have pleiotropic effects including anti-inflammatory and/or antioxidant responses. These pleiotropic effects can have a beneficial role in the post-CPR phase. We tested whether two different types of statins, hydrophilic pravastatin and lipophilic simvastatin, attenuated neurological injury following CA/CPR. The efficacy of pravastatin and simvastatin combination treatment was also assessed.
Isoflurane-anesthetized adult male wild-type C57Bl/6 mice subjected to 8-min CA/CPR were randomized into four groups: control, 2 mg/kg pravastatin, 20 mg/kg simvastatin, or a combination of 3 mg/kg pravastatin and 10 mg/kg simvastatin. Neurobehavioral assessment and histological analyses were performed to assess overall general health condition and neuronal injury, respectively.
Combination treatment with pravastatin and simvastatin significantly reduced neuronal injury in the striatum and hippocampus, reduced cerebral edema, and improved general health at 4 days after CA/CPR. Combination statin treatment upregulated endothelial nitric oxide synthase mRNA in the brain. Pravastatin alone, but not simvastatin alone, improved general health after CA/CPR. Pravastatin was less potent than simvastatin at reducing neuronal injury in the brain.
Combination treatment with two different types of statins at the correct dose may be a promising approach to neuroprotection following CA/CPR.
心脏骤停(CA)后继发心肺复苏(CPR)导致大脑中脆弱区域的神经元发生严重损伤。目前,大多数患者在成功复苏后最终因神经损伤而死亡。他汀类药物具有多种作用,包括抗炎和/或抗氧化反应。这些多效性作用在 CPR 后阶段可能具有有益作用。我们测试了两种不同类型的他汀类药物,亲水性普伐他汀和亲脂性辛伐他汀,是否能减轻 CA/CPR 后的神经损伤。还评估了普伐他汀和辛伐他汀联合治疗的效果。
用异氟烷麻醉成年雄性野生型 C57Bl/6 小鼠进行 8 分钟的 CA/CPR,然后随机分为四组:对照组、2mg/kg 普伐他汀组、20mg/kg 辛伐他汀组或 3mg/kg 普伐他汀和 10mg/kg 辛伐他汀联合治疗组。分别进行神经行为评估和组织学分析,以评估整体一般健康状况和神经元损伤。
普伐他汀和辛伐他汀联合治疗可显著减轻 CA/CPR 后纹状体和海马区的神经元损伤,减轻脑水肿,并改善 CA/CPR 后 4 天的一般健康状况。联合他汀类药物治疗可上调大脑中的内皮型一氧化氮合酶 mRNA。普伐他汀单独使用,而辛伐他汀单独使用,均可改善 CA/CPR 后的一般健康状况。普伐他汀降低大脑神经元损伤的作用弱于辛伐他汀。
以正确剂量联合使用两种不同类型的他汀类药物可能是一种有前途的 CA/CPR 后神经保护方法。