Xiamen Cardiovascular Hospital, Xiamen University, No.2999 Jinshan Road, Huli District, Xiamen, Fujian 361012, China.
NHC Key Laboratory of Hormones and Development, Tianjin Key Laboratory of Metabolic Diseases, Chu Hsien-I Memorial Hospital & Tianjin Institute of Endocrinology, Tianjin Medical University, No.6 Huanrui North Road, Ruijing Street, Beichen District, Tianjin 300134, China.
ACS Appl Mater Interfaces. 2021 Mar 31;13(12):13968-13977. doi: 10.1021/acsami.1c00157. Epub 2021 Mar 19.
Oxidative stress plays an important role in Parkinson's disease (PD) and is considered a therapeutic target for PD. However, most therapeutic antioxidants show limitations due to their low reactive oxygen species (ROS) catalytic properties and low crossing of blood-brain barrier. Herein, the antioxidative activity of Yb and Er double-doped CeO (Yb/Er/CeO) upconversion nanoparticles (UCNPs) is obtained for PD treatment. Doping of Yb and Er ions increases oxygen vacancies, which leads to higher enzymelike catalytic activities compared to CeO nanoparticles alone. Tyrosine hydroxylase protein and glial fibrillary acidic protein expression in substantia nigra and striatum as well as the open-field activity test indicates that Yb/Er/CeO is effective for treatment of PD. The activities of glutathione peroxidase and total antioxidant capacity increase and the production of ROS decreases with Yb/Er/CeO UCNP treatment compared with MPTP-induced injury. This indicates that the mechanism of PD treatment is to catalyze ROS products. There have been no reports to date on the usage of Yb/Er/CeO as an antioxidant for PD treatment. Yb/Er/CeO UCNPs cross the blood-brain barrier and exhibit biocompatibility and antioxidant catalytic properties, which decrease the ROS and effectively help in treating PD.
氧化应激在帕金森病 (PD) 中发挥重要作用,被认为是 PD 的治疗靶点。然而,由于大多数治疗性抗氧化剂的活性氧 (ROS) 催化性能低,且血脑屏障通透性低,因此表现出局限性。在此,我们获得了镱和铒共掺杂氧化铈 (Yb/Er/CeO) 上转换纳米粒子 (UCNP) 用于治疗 PD 的抗氧化活性。Yb 和 Er 离子的掺杂增加了氧空位,与单独的 CeO 纳米粒子相比,其表现出更高的酶样催化活性。纹状体和黑质中酪氨酸羟化酶蛋白和神经胶质纤维酸性蛋白的表达以及旷场活动测试表明,Yb/Er/CeO 对 PD 的治疗有效。与 MPTP 诱导损伤相比,谷胱甘肽过氧化物酶和总抗氧化能力的活性增加,ROS 的产生减少,这表明 PD 治疗的机制是催化 ROS 产物。迄今为止,尚未有报道将 Yb/Er/CeO 用作 PD 治疗的抗氧化剂。Yb/Er/CeO UCNP 可穿过血脑屏障,具有生物相容性和抗氧化催化性能,可降低 ROS 并有效帮助治疗 PD。