Magyar Kálmán, Szende Béla
Department of Pharmacodynamics, Neurochemical Research Unit, Semmelweis University, Hungarian Academy of Sciences, PO Box 370, Budapest 1445, Hungary.
Neurotoxicology. 2004 Jan;25(1-2):233-42. doi: 10.1016/S0161-813X(03)00102-5.
(-)-Deprenyl (selegiline) is an irreversible inhibitor of monoamine oxidase (MAO) B, which was discovered in 1962 and become the "golden standard" of MAO research. Like the other MAO-B inhibitors, it was synthesized as an antidepressant, but in a selective MAO-B inhibitory dose it does not act in depression. It is used in the treatment of Parkinson's disease. (-)-Deprenyl potentiates the effect of dopamine, it has antioxidant activity and prevents the toxicity of the dopaminergic (6-OH-dopamine; 1-methyl-4-phenyl-1,2,3,6-tetrahydro-pyridine (MPTP)), the noradrenergic (DSP-4) and cholinergic (AF64A) neurotoxins after pre-treatment. When (-)-deprenyl was administered with levodopa in a long-term treatment of Parkinsonian patients, it induces adverse events (nausea, dizziness, confusion, hallucination, insomnia and cardiovascular changes), which could be due to dopamine potentiation in dopaminergic systems (limbic system), other than the nigrostriatal pathway. (-)-Deprenyl in much lower concentrations needed to induce MAO-B inhibition (10(-9) to 10(-13) M) potently inhibits MPTP or serum withdrawal induced apoptosis in tissue cultures of neuro-ectodermal origin (PC12, M1, M2058). The (+)-enantiomer of deprenyl lacks of this property. The anti-apoptotic activity of (-)-deprenyl can be prevented by inhibiting the metabolism of the drug with SKF-525A pre-treatment, which suggests that some of the presently unknown metabolites could be responsible for the anti-apoptotic activity. In high concentration (10(-3) M), (-)-deprenyl and its metabolites induce apoptosis in tissue cultures without serum withdrawal (biphasic action). Our findings support the view that 100, or even 1000 times lower dose of (-)-deprenyl can be offered in human therapy to protect, or slow down neuronal degeneration, than it is presently used. With low dose of the drug the dopaminergic adverse events could be avoided, while anti-apoptotic activity might be preserved.
(-)-司来吉兰是单胺氧化酶(MAO)B的不可逆抑制剂,于1962年被发现,成为MAO研究的“金标准”。与其他MAO-B抑制剂一样,它最初是作为抗抑郁药合成的,但在选择性MAO-B抑制剂量下,它对抑郁症无效。它用于治疗帕金森病。(-)-司来吉兰可增强多巴胺的作用,具有抗氧化活性,并能在预处理后预防多巴胺能(6-羟基多巴胺;1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP))、去甲肾上腺素能(DSP-4)和胆碱能(AF64A)神经毒素的毒性。当(-)-司来吉兰与左旋多巴联合用于帕金森病患者的长期治疗时,会引发不良事件(恶心、头晕、意识模糊、幻觉、失眠和心血管变化),这可能是由于多巴胺能系统(边缘系统)而非黑质纹状体通路中的多巴胺增强所致。(-)-司来吉兰在诱导MAO-B抑制所需的浓度低得多(10^-9至10^-13 M)时,能有效抑制神经外胚层来源的组织培养物(PC12、M1、M2058)中MPTP或血清撤除诱导的细胞凋亡。司来吉兰的(+)-对映体缺乏这种特性。(-)-司来吉兰的抗凋亡活性可通过SKF-525A预处理抑制药物代谢来预防,这表明目前一些未知的代谢产物可能是抗凋亡活性的原因。在高浓度(10^-3 M)下,(-)-司来吉兰及其代谢产物在无血清撤除的组织培养物中诱导细胞凋亡(双相作用)。我们的研究结果支持这样一种观点,即在人类治疗中,与目前使用的剂量相比,提供低100倍甚至1000倍剂量的(-)-司来吉兰就可以保护或减缓神经元变性。使用低剂量药物可以避免多巴胺能不良事件,同时可能保留抗凋亡活性。