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用于初发帕金森病患者单药治疗的多巴胺激动剂:与司来吉兰的比较。

Dopamine agonists used as monotherapy in de novo PD patients: comparisons with selegiline.

作者信息

Lieberman A

机构信息

Department of Movement Disorders, Barrow Neurological Institute, St. Joseph's Hospital and Medical Center, Phoenix, Arizona 85013.

出版信息

Neurology. 1992 Apr;42(4 Suppl 4):37-40; discussion 41-8.

PMID:1350073
Abstract

Studies indicate that selegiline, a monoamine oxidase type B inhibitor, slows progression of Parkinson's disease (PD) and delays the need for levodopa. While dopamine agonists also delay the need for levodopa because of their symptomatic, antiparkinsonian effect, only recently has it been proposed that agonists may also have a protective effect. When dopamine agonists are used as monotherapy in newly diagnosed PD patients, fewer patients improve than on levodopa, but fewer patients develop response fluctuations. This might indicate that dopamine agonists have a protective, as well as a symptomatic, effect, as the lack of response fluctuations may indicate that dopamine agonists protect nigral neurons. Response fluctuations may result from destruction of nigral neurons.

摘要

研究表明,单胺氧化酶B型抑制剂司来吉兰可减缓帕金森病(PD)的进展,并推迟左旋多巴的使用需求。虽然多巴胺激动剂因其缓解帕金森症状的作用也能推迟左旋多巴的使用需求,但直到最近才有观点认为激动剂可能也具有保护作用。当多巴胺激动剂用于新诊断的PD患者的单药治疗时,与使用左旋多巴相比,病情改善的患者较少,但出现反应波动的患者也较少。这可能表明多巴胺激动剂既有保护作用,也有缓解症状的作用,因为缺乏反应波动可能意味着多巴胺激动剂对黑质神经元具有保护作用。反应波动可能是黑质神经元被破坏所致。

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