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Is developmental neuropathology of the motor neurons the key to resolving the mystery in motor neuron diseases?

机译:运动神经元的发育神经病理学是解决运动神经元疾病之谜的关键吗?

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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.
机译:近年来,对运动神经元疾病的遗传学研究取得了突飞猛进的进展,但肌萎缩性侧索硬化症和脊髓性肌萎缩症的发病机理仍存在谜团。本期《大脑与发展》上的三篇论文提出了有关脊髓和脑干运动神经元发育神经病理学的有趣话题。在大鼠中进行的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具有修饰作用。在围产期和婴儿突然死亡的受害者中,舌下核的运动神经元和中间神经元的种群变化被证明与脑干呼吸网络的成熟有关。据报道,围产期缺氧缺血性脑病患者存在舌下发育不全和视网膜后增生并存。这些发现可能是解决运动神经元疾病的不确定病理机制的关键。

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