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深入了解铁死亡:与阿尔茨海默病、帕金森病和脑肿瘤的关联,以及纳米材料诱导铁死亡可能的治疗方法。

Deeper insight into ferroptosis: association with Alzheimer's, Parkinson's disease, and brain tumors and their possible treatment by nanomaterials induced ferroptosis.

机构信息

Department of Life Sciences, Hemchandracharya North Gujarat University, Patan, India.

Department of Physics, Faculty of Sciences, University 20 Août 1955, Skikda, Algeria.

出版信息

Redox Rep. 2023 Dec;28(1):2269331. doi: 10.1080/13510002.2023.2269331. Epub 2023 Nov 27.

DOI:10.1080/13510002.2023.2269331
PMID:38010378
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11001282/
Abstract

Ferroptosis is an emerging and novel type of iron-dependent programmed cell death which is mainly caused by the excessive deposition of free intracellular iron in the brain cells. This deposited free iron exerts a ferroptosis pathway, resulting in lipid peroxidation (LiPr). There are mainly three ferroptosis pathways viz. iron metabolism-mediated cysteine/glutamate, and LiPr-mediated. Iron is required by the brain as a redox metal for several physiological activities. Due to the iron homeostasis balance disruption, the brain gets adversely affected which further causes neurodegenerative diseases (NDDs) like Parkinson's and Alzheimer's disease, strokes, and brain tumors like glioblastoma (GBS), and glioma. Nanotechnology has played an important role in the prevention and treatment of these NDDs. A synergistic effect of nanomaterials and ferroptosis could prove to be an effective and efficient approach in the field of nanomedicine. In the current review, the authors have highlighted all the latest research in the field of ferroptosis, specifically emphasizing on the role of major molecular key players and various mechanisms involved in the ferroptosis pathway. Moreover, here the authors have also addressed the correlation of ferroptosis with the pathophysiology of NDDs and theragnostic effect of ferroptosis and nanomaterials for the prevention and treatment of NDDs.

摘要

铁死亡是一种新的、新型的铁依赖性程序性细胞死亡,主要是由脑细胞内自由铁的过度沉积引起的。这种沉积的自由铁发挥铁死亡途径,导致脂质过氧化(LiPr)。主要有三种铁死亡途径,即铁代谢介导的半胱氨酸/谷氨酸和 LiPr 介导的途径。铁作为一种氧化还原金属,对大脑的几种生理活动都很重要。由于铁的动态平衡被破坏,大脑受到不利影响,进而导致神经退行性疾病(NDDs),如帕金森病和阿尔茨海默病、中风以及脑肿瘤,如胶质母细胞瘤(GBS)和神经胶质瘤。纳米技术在预防和治疗这些 NDDs 方面发挥了重要作用。纳米材料与铁死亡的协同作用可能成为纳米医学领域一种有效且高效的方法。在目前的综述中,作者强调了铁死亡领域的所有最新研究,特别是强调了主要分子关键参与者的作用和铁死亡途径中涉及的各种机制。此外,作者还探讨了铁死亡与 NDDs 病理生理学的相关性,以及铁死亡和纳米材料在预防和治疗 NDDs 中的治疗效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9af6/11001282/c41377347f27/YRER_A_2269331_F0008_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9af6/11001282/e546d1e607e8/YRER_A_2269331_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9af6/11001282/e40f261fbd8a/YRER_A_2269331_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9af6/11001282/8a0b271dbb66/YRER_A_2269331_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9af6/11001282/b21ebd0771e3/YRER_A_2269331_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9af6/11001282/92e0dacd7ad9/YRER_A_2269331_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9af6/11001282/58fd42343959/YRER_A_2269331_F0006_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9af6/11001282/c349420e3c4b/YRER_A_2269331_F0007_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9af6/11001282/c41377347f27/YRER_A_2269331_F0008_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9af6/11001282/e546d1e607e8/YRER_A_2269331_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9af6/11001282/e40f261fbd8a/YRER_A_2269331_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9af6/11001282/8a0b271dbb66/YRER_A_2269331_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9af6/11001282/b21ebd0771e3/YRER_A_2269331_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9af6/11001282/92e0dacd7ad9/YRER_A_2269331_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9af6/11001282/58fd42343959/YRER_A_2269331_F0006_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9af6/11001282/c349420e3c4b/YRER_A_2269331_F0007_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9af6/11001282/c41377347f27/YRER_A_2269331_F0008_OC.jpg

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