Chiabrando Deborah, Fiorito Veronica, Petrillo Sara, Tolosano Emanuela
Molecular Biotechnology Center, Department of Molecular Biotechnology and Health Sciences, University of Torino, Turin, Italy.
Front Neurosci. 2018 Oct 9;12:712. doi: 10.3389/fnins.2018.00712. eCollection 2018.
Heme (iron-protoporphyrin IX) is an essential co-factor involved in several biological processes, including neuronal survival and differentiation. Nevertheless, an excess of free-heme promotes oxidative stress and lipid peroxidation, thus leading to cell death. The toxic properties of heme in the brain have been extensively studied during intracerebral or subarachnoid hemorrhages. Recently, a growing number of neurodegenerative disorders have been associated to alterations of heme metabolism. Hence, the etiology of such diseases remains undefined. The aim of this review is to highlight the neuropathological role of heme and to discuss the major heme-regulated pathways that might be crucial for the survival of neuronal cells. The understanding of the molecular mechanisms linking heme to neurodegeneration will be important for therapeutic purposes.
血红素(铁原卟啉IX)是一种必需的辅因子,参与包括神经元存活和分化在内的多种生物学过程。然而,过量的游离血红素会促进氧化应激和脂质过氧化,从而导致细胞死亡。在脑内或蛛网膜下腔出血期间,血红素在大脑中的毒性特性已得到广泛研究。最近,越来越多的神经退行性疾病与血红素代谢改变有关。因此,此类疾病的病因仍不明确。本综述的目的是强调血红素的神经病理学作用,并讨论可能对神经元细胞存活至关重要的主要血红素调节途径。了解将血红素与神经退行性变联系起来的分子机制对于治疗目的将具有重要意义。