Bar-Am Orit, Yogev-Falach Merav, Amit Tamar, Sagi Yotam, Youdim Moussa B H
Technion-Faculty of Medicine, Eve Topf and NPF Centers for Neurodegenerative Diseases, Department of Pharmacology, Haifa, Israel.
J Neurochem. 2004 Jun;89(5):1119-25. doi: 10.1111/j.1471-4159.2004.02425.x.
We have recently shown that the anti-Parkinson-propargyl-containing monoamine oxidase B (MAO-B) inhibitor drug, rasagiline [N-propargyl-(1R)-aminoindan], and its cholinesterase inhibitor derivatives TV3326 and TV3279, regulate amyloid precursor protein (APP) processing by a protein kinase C (PKC)-dependent mechanism in SH-SY5Y neuroblastoma and PC12 cells. In the present study, we investigated the effect of rasagiline and its derivatives on the regulation of the PKC-dependent mechanism and APP processing under in vivo conditions. Administration of rasagiline (0.1 mg/kg) to male C57/BL mice for 14 days significantly decreased membrane-bound holoprotein APP levels in the hippocampus. Additionally, we observed that rasagiline up-regulated p-PKC levels and the expression of alpha and epsilon PKC isozymes in the hippocampus, indicating that the mechanism by which rasagiline affects APP processing may be related to PKC-associated signalling. The results also demonstrate that rasagiline treatment significantly elevated the levels of phosphorylated myristoylated alanine-rich C kinase substrate (p-MARCKS), a major substrate for PKC, as well as the levels of receptors for activated C kinase 1 (RACK1). Similar effects on APP and PKC levels were also demonstrated for the two cholinesterase inhibitor derivatives of rasagiline, TV3326 and TV3279. These results indicate that rasagiline and its derivatives regulate PKC-dependent mechanisms and APP processing. The activation and induction of PKC and MARCKS by these drugs may have a crucial role not only in their neuroprotective activity, but also in their ability to affect neuronal plasticity and spatial learning processes.
我们最近发现,含抗帕金森炔丙基的单胺氧化酶B(MAO-B)抑制剂药物雷沙吉兰[N-炔丙基-(1R)-氨基茚满]及其胆碱酯酶抑制剂衍生物TV3326和TV3279,在SH-SY5Y神经母细胞瘤和PC12细胞中通过蛋白激酶C(PKC)依赖性机制调节淀粉样前体蛋白(APP)的加工。在本研究中,我们研究了雷沙吉兰及其衍生物在体内条件下对PKC依赖性机制调节和APP加工的影响。给雄性C57/BL小鼠连续14天给予雷沙吉兰(0.1mg/kg),可显著降低海马中膜结合全蛋白APP水平。此外,我们观察到雷沙吉兰上调了海马中p-PKC水平以及α和ε PKC同工酶的表达,表明雷沙吉兰影响APP加工的机制可能与PKC相关信号传导有关。结果还表明,雷沙吉兰治疗显著提高了PKC的主要底物磷酸化豆蔻酰化富含丙氨酸的C激酶底物(p-MARCKS)的水平以及活化C激酶1受体(RACK1)的水平。雷沙吉兰的两种胆碱酯酶抑制剂衍生物TV3326和TV3279对APP和PKC水平也有类似影响。这些结果表明,雷沙吉兰及其衍生物调节PKC依赖性机制和APP加工。这些药物对PKC和MARCKS的激活和诱导不仅可能在其神经保护活性中起关键作用,而且在其影响神经元可塑性和空间学习过程的能力中也起关键作用。