Burke R E, Kenyon N
Department of Neurology, Columbia University, New York, New York 10032.
Exp Neurol. 1991 Jul;113(1):63-73. doi: 10.1016/0014-4886(91)90147-5.
Little is known about the alterations in the neurochemical anatomy of the brain in the static encephalopathies of childhood, of which one cause is hypoxia-ischemia. We and others have previously shown in neonatal rodent that experimental hypoxia-ischemia results in an increase in the density of striatal cholinergic neurons (number/mm3). There is a rostrocaudal gradient for this effect within the striatum, with as much as a 50% increase in density caudally. It has not been known what effect this injury has on the distribution of striatal cholinergic neuropil. We have therefore investigated effects on striatal cholinergic neuropil, demonstrated with a monoclonal antibody to choline acetyltransferase (CAT) and the immunoperoxidase technique. Because individual CAT-positive fibers in the striatum are too numerous to be directly counted, we have quantified relative effects on neuropil at the population level using segmented field analysis within the same section. We find that hypoxic-ischemic injury results in a significant increase in the proportion of the injured striatum occupied by high density CAT-positive neuropil staining. This change is persistent, as it is also observed in adult rats. The increase is uniform in the rostrocaudal dimension. Our measure of CAT-positive neuropil staining, being relative, cannot determine whether the observed increase in staining is strictly due to striatal shrinkage with compaction of fibers or whether, in addition, there has been sprouting. The latter possibility is suggested by the lack of a correlation between the degree of shrinkage and changes in area occupied by positive staining. While the functional significance of these changes is not known, they support the concept that striatal cholinergic systems are resistant to hypoxic-ischemic injury and that an abnormal predominance of these systems may play a role in the persistent alterations of motor control observed clinically in this form of injury.
关于儿童静态脑病中大脑神经化学解剖结构的改变,我们知之甚少,其中一个病因是缺氧缺血。我们和其他人之前在新生啮齿动物中发现,实验性缺氧缺血会导致纹状体胆碱能神经元密度增加(数量/立方毫米)。在纹状体内,这种效应存在头尾梯度,尾部密度增加多达50%。目前尚不清楚这种损伤对纹状体胆碱能神经纤维网的分布有何影响。因此,我们用抗胆碱乙酰转移酶(CAT)单克隆抗体和免疫过氧化物酶技术研究了对纹状体胆碱能神经纤维网的影响。由于纹状体中单个CAT阳性纤维数量过多,无法直接计数,我们在同一切片内使用分段视野分析,在群体水平上量化了对神经纤维网的相对影响。我们发现,缺氧缺血损伤导致高密度CAT阳性神经纤维网染色占据的受损纹状体比例显著增加。这种变化是持续性的,在成年大鼠中也观察到。在头尾维度上,增加是均匀的。我们对CAT阳性神经纤维网染色的测量是相对的,无法确定观察到的染色增加是否严格由于纤维压实导致的纹状体萎缩,或者此外是否有发芽现象。后者的可能性由萎缩程度与阳性染色占据面积变化之间缺乏相关性所提示。虽然这些变化的功能意义尚不清楚,但它们支持这样的概念,即纹状体胆碱能系统对缺氧缺血损伤具有抗性,并且这些系统的异常优势可能在这种损伤形式临床上观察到的运动控制持续改变中起作用。