Navigating the treatment landscape of Alzheimer's disease: Current strategies and future directions

Ibrain Pub Date : 2025-05-10 DOI:10.1002/ibra.12197
Tapas Kumar Mohapatra, Reena Rani Nayak, Ankit Ganeshpurkar, Prashant Tiwari, Dileep Kumar
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引用次数: 0

Abstract

Alzheimer's disease (AD), a neurodegenerative disease leading to dementia, lacks a single definitive diagnosis. While current medications only manage symptoms, the ideal treatment would restore cognition. Traditional therapies targeting beta-amyloid haven't yielded significant results, while new approaches target tau protein tangles, protein degradation pathways, inflammation, and neurotrophic factor depletion. Autophagy, a cellular degradation and recycling process, has emerged as a crucial hallmark and contributor to the pathogenesis of AD. Notably, autophagy induction has emerged as a promising therapeutic approach, with inducers like celastrol and caudatin promoting the degradation of toxic protein aggregates. Additionally, innovative drug formulations, such as nanoparticles, are being explored for targeted drug delivery. Research is increasingly focusing on neuroinflammation and developing multi-targeted drugs to address various aspects of AD, potentially leading to preventive strategies in the early stages. This review summarizes the current state and emerging trends in AD drug development.

阿尔茨海默病的治疗前景:当前策略和未来方向
阿尔茨海默病(AD)是一种导致痴呆的神经退行性疾病,缺乏单一的明确诊断。虽然目前的药物只能控制症状,但理想的治疗方法是恢复认知能力。针对-淀粉样蛋白的传统疗法尚未取得显著成果,而新的方法针对tau蛋白缠结、蛋白质降解途径、炎症和神经营养因子耗竭。自噬是一种细胞降解和再循环过程,已成为AD发病的一个重要标志和因素。值得注意的是,自噬诱导已成为一种很有前景的治疗方法,如雷公藤红素和尾状蛋白等诱导剂可促进有毒蛋白质聚集体的降解。此外,创新的药物配方,如纳米颗粒,正在探索靶向药物递送。研究越来越关注神经炎症和开发多靶向药物来解决阿尔茨海默病的各个方面,有可能在早期阶段导致预防策略。本文综述了阿尔茨海默病药物开发的现状和新趋势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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