4.6 Article

Chlorogenic acid alleviates hypoxic-ischemic brain injury in neonatal mice

Journal

NEURAL REGENERATION RESEARCH
Volume 18, Issue 3, Pages 568-576

Publisher

WOLTERS KLUWER MEDKNOW PUBLICATIONS
DOI: 10.4103/1673-5374.350203

Keywords

chlorogenic acid; ferroptosis; glutathione peroxidase 4; lipid peroxidation; neonatal hypoxic-ischemic brain injury; neurons; neuroprotection; oxidative stress; oxygen-glucose deprivation; system Xc(-)

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Recent studies have found that chlorogenic acid (CGA) in coffee has a protective effect on the nervous system, but its role in neonatal hypoxic-ischemic brain injury is still unclear. In this study, a newborn mouse model of hypoxic-ischemic brain injury was established and CGA was injected intraperitoneally. The results showed that CGA intervention effectively reduced cerebral infarct volume, relieved cerebral edema, restored brain tissue structure, and promoted axon growth in injured brain tissue.
Recent studies have shown that chlorogenic acid (CGA), which is present in coffee, has protective effects on the nervous system. However, its role in neonatal hypoxic-ischemic brain injury remains unclear. In this study, we established a newborn mouse model of hypoxic-ischemic brain injury using a modified Rice-Vannucci method and performed intraperitoneal injection of CGA. We found that CGA intervention effectively reduced the volume of cerebral infarct, alleviated cerebral edema, restored brain tissue structure after injury, and promoted axon growth in injured brain tissue. Moreover, CGA pretreatment alleviated oxygen-glucose deprivation damage of primary neurons and promoted neuron survival. In addition, changes in ferroptosis-related proteins caused by hypoxic-ischemic brain injury were partially reversed by CGA. Furthermore, CGA intervention upregulated the expression of the key ferroptosis factor glutathione peroxidase 4 and its upstream glutamate/cystine antiporter related factors SLC7A11 and SLC3A2. In summary, our findings reveal that CGA alleviates hypoxic-ischemic brain injury in neonatal mice by reducing ferroptosis, providing new ideas for the treatment of neonatal hypoxic-ischemic brain injury.

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