Follett Pamela L, Deng Wenbin, Dai Weimin, Talos Delia M, Massillon Leon J, Rosenberg Paul A, Volpe Joseph J, Jensen Frances E
Department of Neurology and Program in Neuroscience, Children's Hospital and Harvard Medical School, Boston, Massachusetts 02115, USA.
J Neurosci. 2004 May 5;24(18):4412-20. doi: 10.1523/JNEUROSCI.0477-04.2004.
Periventricular leukomalacia is a form of hypoxic-ischemic cerebral white matter injury seen most commonly in premature infants and is the major antecedent of cerebral palsy. Glutamate receptor-mediated excitotoxicity is a predominant mechanism of hypoxic-ischemic injury to developing cerebral white matter. We have demonstrated previously the protective effect of AMPA-kainate-type glutamate receptor blockade in a rodent model of periventricular leukomalacia. The present study explores the therapeutic potential of glutamate receptor blockade for hypoxic-ischemic white matter injury. We demonstrate that AMPA receptors are expressed on developing human oligodendrocytes that populate fetal white matter at 23-32 weeks gestation, the period of highest risk for periventricular leukomalacia. We show that the clinically available anticonvulsant topiramate, when administered post-insult in vivo, is protective against selective hypoxic-ischemic white matter injury and decreases the subsequent neuromotor deficits. We further demonstrate that topiramate attenuates AMPA-kainate receptor-mediated cell death and calcium influx, as well as kainate-evoked currents in developing oligodendrocytes, similar to the AMPA-kainate receptor antagonist 6-nitro-7-sulfamoylbenzo-(f)quinoxaline-2,3-dione (NBQX). Notably, protective doses of NBQX and topiramate do not affect normal maturation and proliferation of oligodendrocytes either in vivo or in vitro. Taken together, these results suggest that AMPA-kainate receptor blockade may have potential for translation as a therapeutic strategy for periventricular leukomalacia and that the mechanism of protective efficacy of topiramate is caused at least in part by attenuation of excitotoxic injury to premyelinating oligodendrocytes in developing white matter.
脑室周围白质软化是一种缺氧缺血性脑白质损伤形式,最常见于早产儿,是脑瘫的主要前驱病变。谷氨酸受体介导的兴奋毒性是发育中的脑白质缺氧缺血性损伤的主要机制。我们之前已在脑室周围白质软化的啮齿动物模型中证明了AMPA-海人酸型谷氨酸受体阻断的保护作用。本研究探讨了谷氨酸受体阻断对缺氧缺血性白质损伤的治疗潜力。我们证明,AMPA受体在发育中的人类少突胶质细胞上表达,这些细胞在妊娠23-32周时填充胎儿白质,这是脑室周围白质软化风险最高的时期。我们表明,临床上可用的抗惊厥药物托吡酯在损伤后体内给药时,对选择性缺氧缺血性白质损伤具有保护作用,并减少随后的神经运动缺陷。我们进一步证明,托吡酯可减轻AMPA-海人酸受体介导的细胞死亡和钙内流,以及发育中的少突胶质细胞中海人酸诱发的电流,类似于AMPA-海人酸受体拮抗剂6-硝基-7-氨磺酰基苯并-(f)喹喔啉-2,3-二酮(NBQX)。值得注意的是,NBQX和托吡酯的保护剂量在体内或体外均不影响少突胶质细胞的正常成熟和增殖。综上所述,这些结果表明,AMPA-海人酸受体阻断可能有潜力转化为脑室周围白质软化的治疗策略,托吡酯保护作用的机制至少部分是由于减轻了发育中的白质中未成熟少突胶质细胞的兴奋毒性损伤。