Khwaja O, Volpe J J
Department of Neurology, Children's Hospital Boston, 300 Longwood Ave, Boston, MA 02115, USA.
Arch Dis Child Fetal Neonatal Ed. 2008 Mar;93(2):F153-61. doi: 10.1136/adc.2006.108837.
Cerebral white matter injury, characterised by loss of premyelinating oligodendrocytes (pre-OLs), is the most common form of injury to the preterm brain and is associated with a high risk of neurodevelopmental impairment. The unique cerebrovascular anatomy and physiology of the premature baby underlies the exquisite sensitivity of white matter to the abnormal milieu of preterm extrauterine life, in particular ischaemia and inflammation. These two upstream mechanisms can coexist and amplify their effects, leading to activation of two principal downstream mechanisms: excitotoxicity and free radical attack. Upstream mechanisms trigger generation of reactive oxygen and nitrogen species. The pre-OL is intrinsically vulnerable to free radical attack due to immaturity of antioxidant enzyme systems and iron accumulation. Ischaemia and inflammation trigger glutamate receptor-mediated injury leading to maturation-dependent cell death and loss of cellular processes. This review looks at recent evidence for pathogenetic mechanisms in white matter injury with emphasis on targets for prevention and treatment of injury.
脑白质损伤以少突胶质前体细胞(pre-OLs)缺失为特征,是早产脑损伤最常见的形式,且与神经发育障碍的高风险相关。早产婴儿独特的脑血管解剖结构和生理机能是白质对早产宫外生活异常环境(尤其是缺血和炎症)极度敏感的基础。这两种上游机制可同时存在并放大其效应,导致两种主要下游机制激活:兴奋性毒性和自由基攻击。上游机制触发活性氧和氮物种的产生。由于抗氧化酶系统不成熟和铁蓄积,pre-OL本质上易受自由基攻击。缺血和炎症触发谷氨酸受体介导的损伤,导致成熟依赖性细胞死亡和细胞突起丧失。本综述探讨了白质损伤发病机制的最新证据,重点关注损伤的预防和治疗靶点。