Greulich W, Fenger E
Klinik für Neurologie, Universität Witten/Herdecke, Federal Republic of Germany.
J Neural Transm Suppl. 1995;46:415-21.
After almost 30 years amantadines have reached a definite position in the therapy of Parkinson's disease. Especially in akinetic crisis and in combination with L-Dops amantadine improves the major symptoms of parkinsonism if L-Dopa alone is no more sufficient. Also in cases where L-Dopa treatment is not effective there is reported of a positive reaction on amantadine (Sandyk, 1987). Another advantage is their low side effects and their fast effectiveness. A monotherapy with amantadine is indicated in the early phase of Parkinson's disease and in cases of slight symptoms. According to Kornhuber and Streifler (1992) two thirds of parkinsonian patients react by such a monotherapy with a global improvement of 20 to 40%. After a long-term treatment amantadines are also still effective. In the beginning of the 1970ies opponent statements were made but now a days no larger amantadine study could show a definite decline in initial response to these drugs. Long-term studies with a larger population of patients indicate effects for many years. With additional knowledge about the pathogenesis of Parkinson's disease and about the role of the neurotoxicity though glutamate amantadines as NMDA-receptor antagonists become a great importance as neuroprotective substances.
经过近30年的发展,金刚烷胺在帕金森病治疗中已占据明确地位。尤其是在运动不能危象中,以及与左旋多巴联合使用时,如果单独使用左旋多巴不再足够,金刚烷胺可改善帕金森病的主要症状。在左旋多巴治疗无效的情况下,也有报道称对金刚烷胺有阳性反应(桑迪克,1987年)。另一个优点是它们的副作用低且起效快。金刚烷胺单一疗法适用于帕金森病的早期阶段和症状轻微的情况。根据科尔恩胡伯和施特雷弗勒(1992年)的研究,三分之二的帕金森病患者通过这种单一疗法有整体20%至40%的改善。经过长期治疗,金刚烷胺仍然有效。在20世纪70年代初有反对观点,但如今没有更大规模的金刚烷胺研究能表明对这些药物的初始反应有明显下降。对更多患者群体的长期研究表明其多年来都有效果。随着对帕金森病发病机制以及谷氨酸神经毒性作用的更多了解,作为N-甲基-D-天冬氨酸(NMDA)受体拮抗剂的金刚烷胺作为神经保护物质变得极为重要。