Neuroprotection on ischemic brain injury by Mg<sup>2+</sup>/H<sub>2</sub> released from endovascular Mg implant.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 39280580.
- Also identified by DOI 10.1016/j.bioactmat.2024.08.019 and PMC identifier 11402188.
- Licence recorded as CC BY-NC-ND.
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Abstract
Most acute ischemic stroke patients with large vessel occlusion require stent implantation for complete recanalization. Yet, due to ischemia-reperfusion injury, over half of these patients still experience poor prognoses. Thus, neuroprotective treatment is imperative to alleviate the ischemic brain injury, and a proof-of-concept study was conducted on "biodegradable neuroprotective stent". This concept is premised on the hypothesis that locally released Mg<sup>2+</sup>/H<sub>2</sub> from Mg metal within the bloodstream could offer synergistic neuroprotection against reperfusion injury in distant cerebral ischemic tissues. Initially, the study evaluated pure Mg's neuroactive potential using oxygen-glucose deprivation/reoxygenation (OGD/R) injured neuron cells. Subsequently, a pure Mg wire was implanted into the common carotid artery of the transient middle cerebral artery occlusion (MCAO) rat model to simulate human brain ischemia/reperfusion injury. <i>In vitro</i> analyses revealed that pure Mg extract aided mouse hippocampal neuronal cell (HT-22) in defending against OGD/R injury. Additionally, the protective effects of the Mg wire on behavioral abnormalities, neural injury, blood-brain barrier disruption, and cerebral blood flow reduction in MCAO rats were verified. Conclusively, Mg-based biodegradable neuroprotective implants could serve as an effective local Mg<sup>2+</sup>/H<sub>2</sub> delivery system for treating distant cerebral ischemic diseases.