Hornykiewicz O, Kish S J, Becker L E, Farley I, Shannak K
N Engl J Med. 1986 Aug 7;315(6):347-53. doi: 10.1056/NEJM198608073150602.
We examined histologically and biochemically the brains of two patients with generalized childhood-onset dystonia musculorum deformans. We found no important histologic changes in the basal ganglia, cerebral cortex, higher brain-stem nuclei, locus ceruleus, or raphe nuclei. Similarly, the activity of choline acetyltransferase and the levels of gamma-aminobutyric acid and glutamic acid in the cerebral cortex and basal ganglia were within the control range. In contrast, the norepinephrine concentrations were markedly and consistently decreased in the lateral and posterior hypothalamus, mamillary body, subthalamic nucleus, and locus ceruleus. The serotonin level was subnormal in the dorsal raphe nucleus, as was the dopamine level in the nucleus accumbens and, in one of the two cases, in the striatum. Elevated concentrations of norepinephrine were found in the septum, thalamus, colliculi, red nucleus, and dorsal raphe nucleus; of serotonin, in the globus pallidus, subthalamic nucleus, and locus ceruleus; and of 5-hydroxyindoleacetic acid, in the globus pallidus, subthalamic nucleus, and nuclei raphe centralis inferior and obscurus. The level of homovanillic acid showed little consistent change in the regions examined. We conclude that some of these monoamine changes, especially the pronounced apparent disturbance of noradrenergic brain mechanisms, may represent a basic neurochemical abnormality in dystonia musculorum deformans and may thus be relevant to the pathoneurophysiology and treatment of this disorder.
我们对两名患有全身性儿童期起病的变形性肌张力障碍的患者的大脑进行了组织学和生化检查。我们在基底神经节、大脑皮层、高位脑干核、蓝斑或中缝核中未发现重要的组织学变化。同样,大脑皮层和基底神经节中胆碱乙酰转移酶的活性以及γ-氨基丁酸和谷氨酸的水平均在对照范围内。相比之下,下丘脑外侧和后部、乳头体、丘脑底核和蓝斑中的去甲肾上腺素浓度明显且持续降低。中缝背核中的血清素水平低于正常,伏隔核中的多巴胺水平以及在两例中的一例纹状体中的多巴胺水平也低于正常。在隔区、丘脑、丘、红核和中缝背核中发现去甲肾上腺素浓度升高;在苍白球、丘脑底核和蓝斑中发现血清素浓度升高;在苍白球、丘脑底核以及中缝中央下核和中缝隐核中发现5-羟吲哚乙酸浓度升高。在所检查的区域中,高香草酸水平几乎没有一致的变化。我们得出结论,这些单胺变化中的一些,尤其是去甲肾上腺素能脑机制明显的明显紊乱,可能代表变形性肌张力障碍的一种基本神经化学异常,因此可能与该疾病的病理神经生理学和治疗有关。