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铁死亡在阿尔茨海默病中的作用:机制与治疗潜力(综述)

The role of ferroptosis in Alzheimer's disease: Mechanisms and therapeutic potential (Review).

作者信息

Zeng Heng, Jin Zhaohui

机构信息

Department of Pharmacy, West China Hospital, Sichuan University, Chengdu, Sichuan 610041, P.R. China.

出版信息

Mol Med Rep. 2025 Jul;32(1). doi: 10.3892/mmr.2025.13557. Epub 2025 May 9.

Abstract

Alzheimer's disease (AD) is a prevalent neurodegenerative disorder characterized by insidious onset and progressive symptom deterioration. It extends beyond a simple aging process, involving irreversible and progressive neurological degeneration that impairs brain function through multiple etiologies. Iron dysregulation is implicated in the pathophysiology of AD; however, the precise mechanisms remain unclear. Additionally, vitamin E and selenium are key in regulating ferroptosis through their antioxidant properties. The present review examined the mechanistic pathways by which ferroptosis contributes to AD, the regulatory roles of vitamin E, selenium, ferrostatin‑1, N‑acetylcysteine and curcumin, and their potential as therapeutic agents to mitigate neurodegeneration.

摘要

阿尔茨海默病(AD)是一种常见的神经退行性疾病,其特征为隐匿起病和症状进行性恶化。它不仅仅是一个简单的衰老过程,还涉及不可逆的进行性神经变性,通过多种病因损害脑功能。铁代谢失调与AD的病理生理学有关;然而,确切机制仍不清楚。此外,维生素E和硒通过其抗氧化特性在调节铁死亡中起关键作用。本综述探讨了铁死亡导致AD的机制途径、维生素E、硒、铁抑素-1、N-乙酰半胱氨酸和姜黄素的调节作用,以及它们作为减轻神经变性治疗药物的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/689e/12076055/c6697f40c24c/mmr-32-01-13557-g00.jpg

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