Department of Physiology, Faculty of Medicine, University of Prishtina, Martyr's Boulevard n.n., 10000, Prishtina, Kosova.
J Transl Med. 2018 Feb 7;16(1):25. doi: 10.1186/s12967-018-1399-5.
Hepcidin is emerging as a new important factor in brain iron homeostasis. Studies suggest that there are two sources of hepcidin in the brain; one is local and the other comes from the circulation. Little is known about the molecular mediators of local hepcidin expression, but inflammation and iron-load have been shown to induce hepcidin expression in the brain. The most important source of hepcidin in the brain are glial cells. Role of hepcidin in brain functions has been observed during neuronal iron-load and brain hemorrhage, where secretion of abundant hepcidin is related with the severity of brain damage. This damage can be reversed by blocking systemic and local hepcidin secretion. Studies have yet to unveil its role in other brain conditions, but the rationale exists, since these conditions are characterized by overexpression of the factors that stimulate brain hepcidin expression, such as inflammation, hypoxia and iron-overload.
亚铁调素在脑铁稳态中作为一个新的重要因素而出现。研究表明,脑内有两种亚铁调素来源;一种是局部来源,另一种来自循环。关于局部亚铁调素表达的分子介质知之甚少,但炎症和铁负荷已被证明可诱导脑内亚铁调素表达。脑内亚铁调素的最重要来源是神经胶质细胞。在神经元铁负荷和脑出血期间观察到了亚铁调素在脑功能中的作用,其中大量亚铁调素的分泌与脑损伤的严重程度有关。通过阻断全身和局部亚铁调素分泌可以逆转这种损伤。虽然研究尚未揭示其在其他脑部疾病中的作用,但这种情况是合理的,因为这些疾病的特征是过度表达刺激脑内亚铁调素表达的因素,如炎症、缺氧和铁过载。