Zucca Fabio A, Giaveri Giuseppe, Gallorini Mario, Albertini Alberto, Toscani Marco, Pezzoli Gianni, Lucius Ralph, Wilms Henrik, Sulzer David, Ito Shosuke, Wakamatsu Kazumasa, Zecca Luigi
Institute of Biomedical Technologies-CNR 20090 Segrate (Milano), Italy.
Pigment Cell Res. 2004 Dec;17(6):610-7. doi: 10.1111/j.1600-0749.2004.00201.x.
Neuromelanin (NM) accumulates as a function of age in normal human substantia nigra (SN) but is relatively depleted in the SN of patients with Parkinson disease (PD). Several studies have been performed to further our understanding of the role of NM in neuronal aging and neurodegenerative mechanisms of PD. To this purpose, NM from human SN was isolated and its structure and molecular interactions were investigated. Cysteinyl-dopamine was shown to be one precursor of NM synthesis. A striking affinity of NM for specific metals, lipids, drugs and pesticides was found in vitro, and in animal and human brain postmortem studies. Because of these affinities, NM seems to play a protective role in the human brain by blocking toxic molecules. On the other hand, experiments in cell culture indicate that NM can activate microglia, eliciting the release of cytotoxic factors that can induce neurodegeneration.
神经黑色素(NM)在正常人类黑质(SN)中随年龄增长而积累,但在帕金森病(PD)患者的黑质中相对减少。已经进行了多项研究,以加深我们对NM在神经元衰老和PD神经退行性机制中作用的理解。为此,从人类黑质中分离出NM,并对其结构和分子相互作用进行了研究。半胱氨酰多巴胺被证明是NM合成的一种前体。在体外以及动物和人类脑死后研究中发现,NM对特定金属、脂质、药物和农药具有显著亲和力。由于这些亲和力,NM似乎通过阻断有毒分子在人类大脑中发挥保护作用。另一方面,细胞培养实验表明,NM可以激活小胶质细胞,引发细胞毒性因子的释放,从而诱导神经退行性变。