Lloyd K G
Adv Exp Med Biol. 1977;90:255-66. doi: 10.1007/978-1-4684-2511-6_16.
Postmortem studies in brains from parkinsonian patients consistently reveal a minimum loss of 75% of the nigrostriatal dopamine neurons. This indicates that over a prolonged period, before Parkinson's disease is clinically evident, there is a physiological compensation for the slow loss of dopamine neurons (i.e. compensated stage of Parkinson's disease). Only when the dopamine neuron loss is sufficiently severe (greater than 75% of nigrostriatal dopamine neurons) does the disease become clinically evident (decompensated state). Postmortem examination of Parkinson's disease brains and study of animal models indicate that the following mechanisms may contribute to this CNS compensation: 1) A decrease in striatal cholinergic activity, in an attempt to maintain a critical DA:ACh balance; and 2) A decrease in activity of GABA neurons in the striatum and substantia nigra, resulting in an increased firing rate of nigral dopamine cells. These mechanisms allow the brain to readjust to the initial dopamine cell loss in Parkinson's disease.
对帕金森病患者大脑进行的尸检研究始终显示,黑质纹状体多巴胺神经元至少损失75%。这表明,在帕金森病出现临床症状之前的很长一段时间里,多巴胺神经元的缓慢损失存在生理补偿机制(即帕金森病的代偿期)。只有当多巴胺神经元损失足够严重(超过黑质纹状体多巴胺神经元的75%)时,疾病才会出现临床症状(失代偿状态)。对帕金森病患者大脑的尸检以及动物模型研究表明,以下机制可能有助于这种中枢神经系统的补偿:1)纹状体胆碱能活性降低,试图维持关键的多巴胺:乙酰胆碱平衡;2)纹状体和黑质中γ-氨基丁酸(GABA)神经元的活性降低,导致黑质多巴胺细胞的放电频率增加。这些机制使大脑能够重新适应帕金森病初期的多巴胺细胞损失。