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左旋司来吉兰(司来吉兰)的生化作用。

Biochemical actions of l-deprenyl (selegiline).

作者信息

Lange K W, Riederer P, Youdim M B

机构信息

Department of Clinical Neurochemistry, University of Würzburg.

出版信息

Clin Pharmacol Ther. 1994 Dec;56(6 Pt 2):734-41. doi: 10.1038/clpt.1994.203.

Abstract

l-Deprenyl is a selective, irreversible monoamine oxidase (MAO) type B inhibitor. Dopamine is a relatively good MAO-B substrate in the human brain. Because Parkinson's disease is characterized by a decrease in dopaminergic neurotransmission in the basal ganglia, the selective inhibition of MAO-B should lead to diminished metabolism of dopamine in the nigrostriatal system and a significant increase in the concentration of the neurotransmitter. MAO-B inhibition explains the clinical efficacy of l-deprenyl in the treatment of Parkinson's disease and the prevention of the conversion of protoxins such as 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine, which is oxidized by MAO-B and can cause a parkinsonian syndrome, to their active neurotoxin. In addition, l-deprenyl appears to exhibit other biochemical actions that are independent of its MAO-B activity. These actions may be the basis of the neuroprotective effects of l-deprenyl and may include the inhibition of oxidative stress, an indirect influence on the polyamine binding site of the N-methyl-d-aspartate receptor and the stimulation of neurotrophic factors.

摘要

左旋司来吉兰是一种选择性、不可逆的单胺氧化酶(MAO)B型抑制剂。多巴胺是人脑中相对良好的MAO - B底物。由于帕金森病的特征是基底神经节中多巴胺能神经传递减少,对MAO - B的选择性抑制应导致黑质纹状体系统中多巴胺代谢减少,神经递质浓度显著增加。MAO - B抑制作用解释了左旋司来吉兰在治疗帕金森病以及预防原毒素(如1 - 甲基 - 4 - 苯基 - 1,2,3,6 - 四氢吡啶,其被MAO - B氧化并可导致帕金森综合征)转化为活性神经毒素方面的临床疗效。此外,左旋司来吉兰似乎还表现出其他与其MAO - B活性无关的生化作用。这些作用可能是左旋司来吉兰神经保护作用的基础,可能包括抑制氧化应激、对N - 甲基 - D - 天冬氨酸受体多胺结合位点的间接影响以及神经营养因子的刺激。

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