Cowper-Smith C D, Anger G J A, Magal E, Norman M H, Robertson G S
Department of Pharmacology, Dalhousie University, Sir Charles Tupper Medical Building, 5850 College Street, Halifax, Nova Scotia, Canada B3H 1X5.
Neuroscience. 2008 Aug 26;155(3):864-75. doi: 10.1016/j.neuroscience.2008.05.051. Epub 2008 Jun 10.
We compared the neuroprotective efficacy of a potent and CNS-penetrant cyclin dependent kinase (CDK) and glycogen synthase kinase 3 beta (GSK3beta) inhibitor (Compound 1) in juvenile (postnatal day 21; P21) and adult C57Bl/6 mice (postnatal day 60; P60) using a model of hypoxic-ischemic brain injury (HI). Neuronal cell counts and density measures from brain sections stained with Cresyl Violet revealed that exposure of P21 mice to 60 min of HI resulted in extensive damage to the ipsilateral cornu ammonis 1 (CA1) region of the hippocampus (40% cell loss) and striatum (30% cell loss) 7 days later. Exposure of P60 mice to 40 min of HI produced a similar pattern of cell loss. Intraperitoneal administration of Compound 1 (3 mg/kg) 1, 5 and 9 h after 60 min of HI did not reduce brain injury in P21 mice relative to vehicle controls. By contrast, in P60 mice, this treatment significantly decreased cell loss in the ipsilateral hippocampus (10% cell loss) and striatum (15% loss) relative to vehicle controls. Terminal uridine deoxynucleotidyl transferase (TUNNEL) positive cell counts and infarct volume were also substantially reduced in P60 mice treated with Compound 1. A motor coordination test performed twice weekly until 5 weeks post-HI confirmed that Compound 1 produced long lasting functional recovery. Our results indicate that Compound 1 produced long lasting neuroprotective effects in adult but not juvenile mice suggesting that inhibition of the CDKs and GSK3beta plays a distinct neuroprotective role in the juvenile and adult brain.
我们使用缺氧缺血性脑损伤(HI)模型,比较了一种强效且可穿透中枢神经系统的细胞周期蛋白依赖性激酶(CDK)和糖原合酶激酶3β(GSK3β)抑制剂(化合物1)在幼年(出生后第21天;P21)和成年C57Bl/6小鼠(出生后第60天;P60)中的神经保护效果。用甲酚紫染色的脑切片进行神经元细胞计数和密度测量结果显示,P21小鼠暴露于60分钟的HI后,7天后海马体同侧角回1(CA1)区域(细胞损失40%)和纹状体(细胞损失30%)受到广泛损伤。P60小鼠暴露于40分钟的HI后产生了类似的细胞损失模式。在HI 60分钟后1、5和9小时腹腔注射化合物1(3毫克/千克),相对于载体对照组,并未减少P21小鼠的脑损伤。相比之下,在P60小鼠中,这种治疗相对于载体对照组显著减少了同侧海马体(细胞损失10%)和纹状体(细胞损失15%)中的细胞损失。用化合物1处理的P60小鼠中,末端脱氧核苷酸转移酶(TUNNEL)阳性细胞计数和梗死体积也大幅减少。每周进行两次运动协调测试,直至HI后5周,结果证实化合物1产生了持久的功能恢复。我们的结果表明,化合物1在成年小鼠而非幼年小鼠中产生了持久的神经保护作用,这表明抑制CDK和GSK3β在幼年和成年大脑中发挥着不同的神经保护作用。