神经保护
胶质增生
医学
脑损伤
药理学
麻醉
细胞凋亡
神经科学
内科学
病理
生物
生物化学
作者
Mingchu Fang,Shishuang Jiang,Jianghu Zhu,Xiaoqin Fu,Yingying Hu,Shulin Pan,Huai Jiang,Jian Lin,Junhui Yuan,Peijun Li,Zhenlang Lin
标识
DOI:10.1016/j.expneurol.2020.113393
摘要
Neonatal hypoxic-ischemic (HI) brain injury remains a devastating clinical disease associated with high mortality and lifetime disability. Neonatal HI injury damages the architecture of neurovascular unit (NVU), thus, therapy targeting the NVU may provide effective neuroprotection against HI. This study was designed to investigate whether fibroblast growth factor 10 (FGF10) protected the NVU against HI and afforded observable neuroprotection in a rat model of neonatal HI brain injury. The results showed that FGF10 treatment significantly reduced brain damage post HI, characterized by reduction in brain infarct volume and tissue loss. Further interesting findings showed that FGF10 treatment exerted neuroprotective effects on HI brain injury in neonate rats through protecting the NVU against HI, evidenced by inhibition of neuronal cell apoptosis, suppression of gliosis, and amelioration of blood-brain barrier disruption. Collectively, our study indicates that FGF10 treatment exhibits great potential for protecting NVU against HI and attenuates neonatal brain injury, suggesting a potential novel therapeutic agent to this disease.
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