Journal
BRAIN AND BEHAVIOR
Volume -, Issue -, Pages -Publisher
WILEY
DOI: 10.1002/brb3.3179
Keywords
Ga-68-citrate; cottonseed oil (CSO); ferroptosis; ischemic stroke; neuroprotection; positron emission tomography (PET)
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This study found that cottonseed oil (CSO) can alleviate ferroptosis caused by cerebral ischemic injury in rats. CSO treatment reduces neurological dysfunction, infarct volume, neuronal injuries, and BBB integrity disruption. It also up-regulates anti-ferroptosis proteins and decreases ferroptosis-related proteins, as well as improves mitochondrial destruction induced by ischemic stroke. This provides new evidence for the potential therapeutic mechanism of CSO neuroprotection against ischemic stroke.
IntroductionFerroptosis has recently been recognized as a new cause of ischemia reperfusion injury due to blood-brain barrier (BBB) disruption followed by secondary iron-loaded transferrin (TF) influx. As a novel and independent cell death pathway, ferroptosis was characterized by iron-dependent lipid peroxidation, decline of GSH, GPX4, and shrinking mitochondria. Cottonseed oil (CSO), a liposoluble solvent, can alleviate ischemia stroke injuries and oxidative stress. However, the effect of CSO on ischemic stroke-induced ferroptosis has not been explored. In this study, we investigated the effect of CSO on ferroptosis caused by cerebral ischemic injury in rats. MethodsWe conducted the subcutaneous injection of 1.3 mL/kg CSO every other day for 3 weeks on rats with middle cerebral artery occlusion-reperfusion (MCAO-R) injury. We used Garcia Test, TTC staining, HE, Nissl and NeuN staining, Evans blue test, Ga-68-citrate PET, Western blot, immunofluorescence staining, Elisa kits, and transmission electron microscopy to detect the infarct volume, neural injuries, and ferroptosis-related indexes. ResultsCSO treatment could significantly ameliorate MCAO-R-induced neurological dysfunction in a male rat model. Furthermore, it reduced infarct volume and neuronal injuries; protected BBB integrity; reduced the influx of iron ion, TF, and TF receptors; up-regulated anti-ferroptosis proteins (GPX4, xCT, HO1, FTH1), while down-regulating ferroptosis-related protein ACSL4; increased the activity of GSH and SOD; and decreased MDA and LPO levels. Mitochondrial destruction induced by ischemic stroke was also alleviated by CSO treatment. ConclusionCSO treatment can alleviate ischemic stroke injury via ferroptosis inhibition, which provides a new potential therapeutic mechanism for CSO neuroprotection against ischemic stroke.
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