Burke R E, Karanas A L
Department of Neurology, College of Physicians and Surgeons, Columbia University, New York, NY.
Ann Neurol. 1990 Jan;27(1):81-8. doi: 10.1002/ana.410270113.
Although the static encephalopathies of childhood are common, little is known of the underlying alterations in the neurochemical anatomy of the brain. Using quantitative morphological techniques, we examined the effect of perinatal hypoxia-ischemia on the number and distribution of cholinergic (ACh) neurons in a unilateral experimental striatal lesion in rats. The striatal pathology simulates status marmoratus, a recognized correlate of human dystonic cerebral palsy. We found that striatal injury results in a mean 22% decrease in the number of ACh neurons at the age of 3 to 4 weeks. The loss of neurons was relatively less than the volume loss, resulting in a mean 16% increase in neuron density. This effect was not uniform throughout the striatum; it was more pronounced caudally, resulting in a mean 52% increase in density in the most caudal striatal plane. These changes in immature rats were also seen in adult rats, indicating that there were lasting alterations in striatal cholinergic morphology. Hypoxic-ischemic injury to the striatum also resulted in a persistent decrease in the mean area of ACh neurons. The increased density of these neurons may imply that they are relatively resistant to hypoxic-ischemic injury. These findings may be relevant to the observation that anticholinergic drugs are among the most effective for treating dystonias, including those observed in static encephalopathies.
尽管儿童期的静态脑病很常见,但对于大脑神经化学解剖结构的潜在改变却知之甚少。我们运用定量形态学技术,研究了围产期缺氧缺血对大鼠单侧实验性纹状体损伤中胆碱能(ACh)神经元数量和分布的影响。纹状体病变模拟大理石样状态,这是一种公认的与人类张力障碍性脑瘫相关的情况。我们发现,在3至4周龄时,纹状体损伤导致ACh神经元数量平均减少22%。神经元的损失相对小于体积损失,导致神经元密度平均增加16%。这种效应在整个纹状体内并不均匀;在尾部更为明显,导致最尾端纹状体平面的密度平均增加52%。未成熟大鼠的这些变化在成年大鼠中也可见,表明纹状体胆碱能形态存在持久改变。纹状体的缺氧缺血损伤还导致ACh神经元的平均面积持续减少。这些神经元密度的增加可能意味着它们对缺氧缺血损伤相对具有抗性。这些发现可能与以下观察结果相关:抗胆碱能药物是治疗张力障碍(包括在静态脑病中观察到的那些)最有效的药物之一。