Hayashi Masaharu
Brain Dev. 2010 Apr;32(4):265-7. doi: 10.1016/j.braindev.2009.12.001. Epub 2009 Dec 30.
Recently, genetic analyses on motor neurons diseases have advanced leaps and bounds, but mysteries still remain in the pathogenesis of amyotrophic lateral sclerosis and spinal muscular atrophy. Three papers in this issue of Brain and Development presented intriguing topics on the developmental neuropathology of motor neurons in the spinal cord and brainstem. Neonatal asphyxia experiments in rats indicated the modification of brainstem monoaminergic neuron systems in the development and repair of spinal motor neurons. In the victims of sudden perinatal and infant death, population changes in motor neurons and interneurons in the hypoglossal nucleus were shown to be involved in the disturbed maturation of the respiratory network in the brainstem. The coexistence of hypoglossal hypoplasia and hyperplasia of the area postrema was reported in a case of perinatal hypoxic ischemic encephalopathy. These findings are likely to be a key to resolving the undetermined pathological mechanisms of motor neuron diseases.
最近,对运动神经元疾病的基因分析取得了长足进展,但肌萎缩侧索硬化症和脊髓性肌萎缩症的发病机制仍存在谜团。本期《脑与发育》中的三篇论文提出了关于脊髓和脑干中运动神经元发育神经病理学的有趣话题。大鼠新生儿窒息实验表明,脑干单胺能神经元系统在脊髓运动神经元的发育和修复中发生了改变。在围产期和婴儿猝死的受害者中,舌下神经核中运动神经元和中间神经元的数量变化被证明与脑干呼吸网络成熟障碍有关。在一例围产期缺氧缺血性脑病病例中,报告了舌下神经发育不全与最后区增生并存的情况。这些发现可能是解决运动神经元疾病尚未明确的病理机制的关键。