Department of Pharmacy, "G. d'Annunzio" University of Chieti-Pescara, via dei Vestini 31, 66100 Chieti, Scalo (Chieti), Italy.
Department of Pharmacy, "G. d'Annunzio" University of Chieti-Pescara, via dei Vestini 31, 66100 Chieti, Scalo (Chieti), Italy.
Neuropeptides. 2018 Oct;71:11-20. doi: 10.1016/j.npep.2018.06.002. Epub 2018 Jun 19.
Neurodegenerative diseases share a common pathogenetic mechanism involving aggregation and deposition of misfolded proteins, oxidative stress, metal dyshomeostasis, and glutamate exicitotoxicity, which lead to progressive dysfunction of central nervous system (CNS). A potential strategy to counteract these deleterious events at neuronal level is represented by the employment of a novel class of multi-target therapeutic agents that selectively and simultaneously hit these targets In this paper, we report the metal binding and antioxidant properties of a novel metal-protein attenuating peptide, GSH-LD, a tetrapeptide obtained by linking glutathione, a well-known antioxidant tripeptide, to L-Dopa. Results demonstrated that GSH-LD possesses chelating capabilities in order to selectively target the excess of metals without interfere with metal-containing antioxidant enzymes. Moreover, antioxidant assays revealed a large contribution of GSH-LD to restore the antioxidant defences of damaged neuronal cells.
神经退行性疾病具有共同的发病机制,涉及错误折叠蛋白质的聚集和沉积、氧化应激、金属动态平衡失调和谷氨酸兴奋性毒性,导致中枢神经系统(CNS)的进行性功能障碍。一种对抗神经元水平这些有害事件的潜在策略是使用新型多靶治疗剂,这些治疗剂选择性地同时作用于这些靶点。在本文中,我们报告了一种新型金属蛋白衰减肽 GSH-LD 的金属结合和抗氧化特性,GSH-LD 是通过将谷胱甘肽(一种众所周知的抗氧化三肽)与 L-多巴连接而获得的四肽。结果表明,GSH-LD 具有螯合能力,以便选择性地针对多余的金属,而不干扰含金属的抗氧化酶。此外,抗氧化测定显示 GSH-LD 对恢复受损神经元细胞的抗氧化防御有很大贡献。