Nihei K, Kowall N W
Neurology Service, Massachusetts General Hospital, Boston 02114.
Neurosci Lett. 1993 Sep 3;159(1-2):67-70. doi: 10.1016/0304-3940(93)90800-z.
We performed a quantitative histochemical study of neuropeptide Y (NPY) immunoreactivity in postmortem human brain to further define patterns of neuronal degeneration in amyotrophic lateral sclerosis (ALS). The density of NPY fibers was decreased in ALS motor cortex but not in other cortical regions or striatum. Although, the density of cortical NPY neurons was unchanged in high grade cases, neurons were shrunken and atrophic with pruned dendrites. NPY neurons are less severely affected than parvalbumin neurons which are severely depleted in ALS cortex. This differential involvement of local circuit neurons suggests that a simple excitotoxic model may not adequately explain patterns of neuronal loss in ALS.
我们对死后人类大脑中的神经肽Y(NPY)免疫反应性进行了定量组织化学研究,以进一步明确肌萎缩侧索硬化症(ALS)中神经元变性的模式。ALS运动皮层中NPY纤维的密度降低,但在其他皮层区域或纹状体中未降低。尽管在高级别病例中皮层NPY神经元的密度未发生变化,但神经元出现萎缩,树突减少。与在ALS皮层中严重减少的小白蛋白神经元相比,NPY神经元受影响较轻。局部回路神经元的这种差异受累表明,简单的兴奋性毒性模型可能无法充分解释ALS中神经元丢失的模式。