De Lean J, Deck J H
Can J Neurol Sci. 1976 Aug;3(3):167-73. doi: 10.1017/s0317167100025695.
The post-mortem examination of the nervous system of a patient with Shy-Drager syndrome successfully treated with levodopa (Sharpe et al, 1972) revealed features of striato-nigral degeneration and amyotrophic lateral sclerosis, a cerebellar system degeneration and a loss of approximately 75% of sympathetic preganglionic neurons. Lewy bodies were not present and no detectable changes were observed in the sympathetic prevertebral ganglia. While the limited and transient beneficial effect of levodopa on the bradykinesia in our case is possibly due to the progressive loss of striatal dopaminergic receptors seen in striatonigral degeneration, we propose that in Shy-Drager syndrome, levodopa therapy benefits orthostatic hypotension because of a suppression of the central depressor action of this drug. This suppression is attributable to functional disconnection of sympathetic ganglia secondary to the loss of preganglionic neurons or to degeneration of central autonomic catecholaminergic systems.
对一名用左旋多巴成功治疗的夏伊-德雷格综合征患者的神经系统进行尸检(夏普等人,1972年),发现有纹状体黑质变性和肌萎缩侧索硬化症的特征、小脑系统变性以及约75%的交感神经节前神经元缺失。未发现路易小体,交感神经椎前神经节也未观察到可检测到的变化。虽然在我们的病例中左旋多巴对运动迟缓的有限且短暂的有益作用可能是由于纹状体黑质变性中纹状体多巴胺能受体的逐渐丧失,但我们认为在夏伊-德雷格综合征中,左旋多巴治疗对体位性低血压有益是因为该药物的中枢降压作用受到抑制。这种抑制归因于节前神经元丧失继发的交感神经节功能断开或中枢自主儿茶酚胺能系统的变性。