» Articles » PMID: 35992267

Neuronal Ferroptosis After Intracerebral Hemorrhage

Overview
Specialty Biology
Date 2022 Aug 22
PMID 35992267
Authors
Affiliations
Soon will be listed here.
Abstract

Intracerebral hemorrhage (ICH) is a devastating form of stroke with high rates of morbidity, mortality, and disability. It induces cell death that is responsible for the secondary brain injury (SBI). The underlying mechanism of SBI after ICH is still unclear, and whether it is related to iron overload is worthy to be discussed. Ferroptosis is an iron-dependent non-apoptotic modes of cell death and plays a particularly important role in the occurrence and progression of ICH. Many ICH-induced regulators and signalling pathways of ferroptosis have been reported as promising targets for treating ICH. In this article, we review the definition, characteristics, and inhibition methods of neuronal ferroptosis caused by iron deposition after ICH, and review the biomarkers for ferroptosis.

Citing Articles

Taurine Attenuates Neuronal Ferroptosis by CSF-Derived Exosomes of GABABR Encephalitis Through GABABR/NF2/P-YAP Pathway.

Zhang C, Zhou T, Qiao S, Lu L, Zhu M, Wang A Mol Neurobiol. 2025; .

PMID: 40085353 DOI: 10.1007/s12035-025-04819-3.


Neuroinflammation and iron metabolism after intracerebral hemorrhage: a glial cell perspective.

Ju J, Hang L Front Neurol. 2025; 15:1510039.

PMID: 39882361 PMC: 11774705. DOI: 10.3389/fneur.2024.1510039.


The role of ACSL4 in stroke: mechanisms and potential therapeutic target.

Zhuo B, Qin C, Deng S, Jiang H, Si S, Tao F Mol Cell Biochem. 2024; .

PMID: 39496916 DOI: 10.1007/s11010-024-05150-6.


Celastrol alleviates secondary brain injury following intracerebral haemorrhage by inhibiting neuronal ferroptosis and blocking blood-brain barrier disruption.

Wei M, Liu Y, Li D, Wang X, Wang X, Li Y IBRO Neurosci Rep. 2024; 17:161-176.

PMID: 39220228 PMC: 11362646. DOI: 10.1016/j.ibneur.2024.08.003.


In situ implantable DNA hydrogel for diagnosis and therapy of postoperative rehemorrhage following intracerebral hemorrhage surgery.

Yu W, Gong E, Wang C, Che C, Zhao Y, Wu X Sci Adv. 2024; 10(33):eado3919.

PMID: 39141742 PMC: 11323940. DOI: 10.1126/sciadv.ado3919.


References
1.
Xie L, Zheng W, Xin N, Xie J, Wang T, Wang Z . Ebselen inhibits iron-induced tau phosphorylation by attenuating DMT1 up-regulation and cellular iron uptake. Neurochem Int. 2012; 61(3):334-40. DOI: 10.1016/j.neuint.2012.05.016. View

2.
Gao M, Monian P, Pan Q, Zhang W, Xiang J, Jiang X . Ferroptosis is an autophagic cell death process. Cell Res. 2016; 26(9):1021-32. PMC: 5034113. DOI: 10.1038/cr.2016.95. View

3.
Ansari S, Memon M, Brohi N, Tahir A . N-acetylcysteine in the Management of Acute Exacerbation of Chronic Obstructive Pulmonary Disease. Cureus. 2019; 11(11):e6073. PMC: 6892576. DOI: 10.7759/cureus.6073. View

4.
Zhang X, Liu T, Xu S, Gao P, Dong W, Liu W . A pro-inflammatory mediator USP11 enhances the stability of p53 and inhibits KLF2 in intracerebral hemorrhage. Mol Ther Methods Clin Dev. 2021; 21:681-692. PMC: 8178085. DOI: 10.1016/j.omtm.2021.01.015. View

5.
Gao M, Monian P, Quadri N, Ramasamy R, Jiang X . Glutaminolysis and Transferrin Regulate Ferroptosis. Mol Cell. 2015; 59(2):298-308. PMC: 4506736. DOI: 10.1016/j.molcel.2015.06.011. View