1. Neuroprotective effect of apigenin against hypoxic-ischemic brain injury in neonatal rats via activation of the PI3K/Akt/Nrf2 signaling pathway
- Author
-
Jianghu Zhu, Changchang Fu, Luyao Li, Kun Lin, Hongzeng Wang, Xiaoqin Fu, Jiali Huang, Yihui Zheng, Zhenlang Lin, Peijun Li, Wei Lin, and Ting-Ting Chen
- Subjects
0301 basic medicine ,Antioxidant ,business.industry ,medicine.medical_treatment ,General Medicine ,Pharmacology ,medicine.disease ,Neuroprotection ,Cerebral edema ,03 medical and health sciences ,chemistry.chemical_compound ,030104 developmental biology ,0302 clinical medicine ,chemistry ,In vivo ,Apoptosis ,Apigenin ,medicine ,business ,Protein kinase B ,030217 neurology & neurosurgery ,PI3K/AKT/mTOR pathway ,Food Science - Abstract
Neonatal hypoxic-ischemic (HI) brain injury can lead to mortality and severe long-term disabilities including cerebral palsy and brain injury. However, the treatment options for neonatal hypoxic-ischemic (HI) brain injury are limited. Apigenin is abundantly present in vegetables, celery, and chamomile tea with diverse biological functions, such as anti-inflammatory, anti-apoptotic, antioxidant, and anticancer effects. However, it has not yet been reported whether apigenin exerts a neuroprotective effect against neonatal hypoxic-ischemic (HI) brain injury. In this study, we investigated whether apigenin could ameliorate HI brain injury and explored the associated mechanism using in vivo experiments. We found that apigenin remarkably reduced the infarct volume and ameliorated cerebral edema, decreased inflammatory response, inhibited apoptosis, promoted the recovery of tissue structure, and improved prognosis following HI brain injury. Mechanistically, we found that apigenin exerted a neuroprotective effect against HI brain injury by activating the PI3K/Akt/Nrf2 pathway. In summary, all these results demonstrate that apigenin could be a potential therapeutic approach for neonatal hypoxic-ischemic (HI) brain injury.
- Published
- 2021
- Full Text
- View/download PDF