Nath Arnab Kumar, Ghatak Arnab, Dey Abhishek, Dey Somdatta Ghosh
Indian Association for the Cultivation of Science 2A & 2B, Raja S. C. Mullick Road, Jadavpur Kolkata 700032 India
Chem Sci. 2020 Dec 22;12(5):1924-1929. doi: 10.1039/d0sc06258h.
The degradation of neurotransmitters is a hallmark feature of Alzheimer's disease (AD). Copper bound Aβ peptides, invoked to be involved in the pathology of AD, are found to catalyze the oxidation of serotonin (5-HT) by HO. A combination of EPR and resonance Raman spectroscopy reveals the formation of a Cu(ii)-OOH species and a dimeric, EPR silent, CuO bis-μ-oxo species under the reaction conditions. The Cu(ii)-OOH species, which can be selectively formed in the presence of excess HO, is the reactive intermediate responsible for 5-HT oxidation. HO produced by the reaction of O with reduced Cu(i)-Aβ species can also oxidize 5-HT. Both these pathways are physiologically relevant and may be involved in the observed decay of neurotransmitters as observed in AD patients.
神经递质的降解是阿尔茨海默病(AD)的一个标志性特征。据认为参与AD病理学的铜结合β淀粉样肽(Aβ)被发现可催化5-羟色胺(5-HT)被HO氧化。电子顺磁共振(EPR)和共振拉曼光谱相结合揭示了在反应条件下形成了一种Cu(II)-OOH物种以及一种二聚体、EPR沉默的CuO双μ-氧物种。可以在过量HO存在下选择性形成的Cu(II)-OOH物种是负责5-HT氧化的反应中间体。由O与还原态的Cu(I)-Aβ物种反应产生的HO也可氧化5-HT。这两条途径在生理上都是相关的,并且可能与AD患者中观察到的神经递质衰变有关。