Rinne J O
Department of Neurology, University of Turku, Finland.
Mov Disord. 1993;8 Suppl 1:S31-5. doi: 10.1002/mds.870080507.
Neuronal loss in the substantia nigra of patients with Parkinson's disease (PD) does not occur evenly throughout the nucleus: the ventrolateral part of the substantia nigra degenerates more severely, whereas the medial part is relatively preserved. This pattern of nigral neuronal loss is compatible with the uneven loss of dopamine in the striatum (the putamen more affected than the caudate nucleus). The predominant loss of ventrolateral nigrostriatal projections in PD, leading to substantial loss of dopamine especially in the putamen, is thought to contribute to the motor symptoms of the patients. On the other hand, the more medial nigral projections may be involved in the cognitive symptoms of patients. Selegiline (L-deprenyl) has been shown to delay the need to initiate levodopa therapy in early PD, and selegiline has also been suggested to increase the survival of PD patients. These observations have led to the proposal of selegiline's neuron-saving effect in PD. There is some pathological evidence supporting the better survival of nigral neurons in PD patients treated with selegiline as compared with those without such treatment. Further studies are, however, needed to elucidate this question more clearly.
帕金森病(PD)患者黑质中的神经元丢失在整个核团中并不均匀:黑质腹外侧部分退化更严重,而内侧部分相对保留。这种黑质神经元丢失模式与纹状体中多巴胺的不均匀丢失(壳核比尾状核受影响更严重)相一致。PD中腹外侧黑质纹状体投射的主要丢失,导致多巴胺大量丢失,尤其是在壳核中,被认为是导致患者运动症状的原因。另一方面,黑质更内侧的投射可能与患者的认知症状有关。司来吉兰(L-司立吉林)已被证明可延迟早期PD患者开始左旋多巴治疗的时间,并且有人提出司来吉兰还可提高PD患者的生存率。这些观察结果导致了司来吉兰在PD中具有神经保护作用的提议。有一些病理学证据支持与未接受此类治疗的PD患者相比,接受司来吉兰治疗的患者黑质神经元存活率更高。然而,需要进一步研究以更清楚地阐明这个问题。