Traumatic Brain Injury |
Controlled cortical impact (CCI) |
/ |
ACSL4 expression level increased |
[66] |
CCI |
Baicalein |
Decreased ferroptotic PE oxidation |
[67] |
Ischemic stroke |
Middle cerebral artery occlusion (MCAO) |
/ |
ACSL4 increased after decreasing 1–3 h of ischemia |
[46] |
MCAO |
liproxstatin-1/Rosiglitazo-ne/ |
Lipid peroxidation index was significantly inhibited in comparison with untreated group |
[73] |
Hemorrhagic stroke |
Oxygen and glucose deprivation (OGD) |
/ |
ACSL4 mRNA expression was significantly increased |
[46] |
OGD |
Paeonol |
Paeonol inhibited the expression of ACSL4 |
[50] |
Alzheimer’s disease |
APPswe transgenic mice |
/ |
Aβ accumulates in brain tissue due to lipid peroxidation |
[74] |
APPswe/PSEN1dE9 (APP/PS1) double transgene mice |
tetrahydroxy stilbene glycoside (TSG) |
TSG inhibited the expression of ACSL4 |
[75] |
Parkinson’s disease |
PD mice model |
1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) |
The expression of ACSL4 significantly increased |
[76] |
PD mice model |
β-hydroxybutyrate (BHB) |
BHB inhibits ferroptosis in PD model |
[77] |
Spinal cord injury |
Spinal cord |
Edaravone |
Reduces ACSL4 levels |
[54] |
contusion injury model |
Multiple sclerosis |
Experimental autoimmune encephalitis (EAE) model |
ACSL4-KO |
Knocking down the ACSL4 gene considerably reduced the severity of EAE and the clinical score of EAE mice |
[78] |