Yang Dongxin, Deng Zhuofen, Zhou Hai, Zhang Qingshang, Zhang Xibing, Gong Jun
Central Laboratory of YunFu People's Hospital, YunFu Key Laboratory of Brain Diseases Research, Yunfu, Guangdong, China.
Department of Pharmacy, YunFu People's Hospital, Yunfu, Guangdong, China.
Front Cell Dev Biol. 2025 Mar 24;13:1562565. doi: 10.3389/fcell.2025.1562565. eCollection 2025.
Alzheimer's disease (AD) is one of the neurodegenerative disorders, characterized by complex pathogenic mechanisms, including the deposition of beta-amyloid protein and hyperphosphorylation of Tau protein. There is currently a lack of effective therapeutic approaches for AD treatment. The aim of this study was to design exosomes (EXO) as a specifically designed carrier able to carry Curcumin (Cur) and Methylene Blue (MB) to improve cognitive function and to elucidate its underlying mechanisms. Our study results indicated that EXO-Cur+MB inhibited Tau protein phosphorylation by activating the AKT/GSK-3β pathway, while reversing cognitive dysfunction in AD mice by reducing apoptosis induced by okadaic acid (OA). Thus, our results suggested that EXO-Cur+MB would be of potential use for the treatment of AD.
阿尔茨海默病(AD)是一种神经退行性疾病,其特征在于复杂的致病机制,包括β-淀粉样蛋白的沉积和Tau蛋白的过度磷酸化。目前缺乏有效的AD治疗方法。本研究的目的是设计外泌体(EXO)作为一种专门设计的载体,能够携带姜黄素(Cur)和亚甲蓝(MB)以改善认知功能并阐明其潜在机制。我们的研究结果表明,EXO-Cur+MB通过激活AKT/GSK-3β途径抑制Tau蛋白磷酸化,同时通过减少冈田酸(OA)诱导的细胞凋亡来逆转AD小鼠的认知功能障碍。因此,我们的结果表明EXO-Cur+MB在AD治疗中具有潜在用途。