Dominiak Agnieszka, Wilkaniec Anna, Wroczyński Piotr, Adamczyk Agata
Department of Cellular Signaling, Mossakowski Medical Research Centre Polish Academy of Sciences, Pawińskiego 5 St., 02-106 Warsaw, Poland.
Curr Neuropharmacol. 2016;14(3):282-99. doi: 10.2174/1570159x14666151223100011.
Selenium (34Se), an antioxidant trace element, is an important regulator of brain function. These beneficial properties that Se possesses are attributed to its ability to be incorporated into selenoproteins as an amino acid. Several selenoproteins are expressed in the brain, in which some of them, e.g. glutathione peroxidases (GPxs), thioredoxin reductases (TrxRs) or selenoprotein P (SelP), are strongly involved in antioxidant defence and in maintaining intercellular reducing conditions. Since increased oxidative stress has been implicated in neurological disorders, including Parkinson's disease, Alzheimer's disease, stroke, epilepsy and others, a growing body of evidence suggests that Se depletion followed by decreased activity of Se-dependent enzymes may be important factors connected with those pathologies. Undoubtedly, the remarkable progress that has been made in understanding the biological function of Se in the brain has opened up new potential possibilities for the treatment of neurological diseases by using Se as a potential drug. However, further research in the search for optimal Se donors is necessary in order to achieve an effective and safe therapeutic income.
硒(34Se)是一种抗氧化微量元素,是脑功能的重要调节剂。硒所具有的这些有益特性归因于其作为氨基酸掺入硒蛋白的能力。几种硒蛋白在大脑中表达,其中一些,如谷胱甘肽过氧化物酶(GPxs)、硫氧还蛋白还原酶(TrxRs)或硒蛋白P(SelP),在抗氧化防御和维持细胞间还原状态方面发挥着重要作用。由于氧化应激增加与包括帕金森病、阿尔茨海默病、中风、癫痫等在内的神经疾病有关,越来越多的证据表明,硒缺乏以及随后硒依赖性酶活性降低可能是与这些疾病相关的重要因素。毫无疑问,在理解硒在大脑中的生物学功能方面所取得的显著进展为将硒作为潜在药物治疗神经疾病开辟了新的潜在可能性。然而,为了获得有效且安全的治疗效果,有必要进一步研究寻找最佳的硒供体。