Fu Guanglei, Kang Xuedi, Lin Songjun
Infectious Disease Department, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, China.
The Fourth Clinical Medical College & ShenZhen Traditional Chinese Medicine Hospital, GuangZhou University of Chinese Medicine, 1 Fuhua Road, Futian District, Shenzhen, China.
Biochem Genet. 2024 Oct 8. doi: 10.1007/s10528-024-10936-w.
Glycyrrhizic acid (GA), one of the main active substances in Glycyrrhiza, has anti-inflammatory, anti-viral, and neuroprotective effects. GA can significantly reduce cerebral infarction size in middle cerebral artery occlusion (MCAO) rats and suppress inflammatory responses. However, the underlying mechanism by which GA protects the neuronal system remains poorly understood. Cell proliferation and viability were tested using CCK-8 and Edu assays. The effects of GA on apoptosis were detected using flow cytometry and Tunel assays. Western blotting was performed to assess protein expression. Behavioral experiments were conducted using the Morris water maze and rotation tests. Infarct size was observed using TTC staining. We report that GA protects neurons by inhibiting apoptosis, mainly through the PI3K/AKT pathway in oxygen-glucose deprivation/reoxygenation (OGD/R) and MCAO rat models. GA increases the viability and proliferation of oxygen- and glucose-deprived hippocampal neurons. Hippocampal neuron apoptosis decreased after GA treatment in vitro and in vivo. Furthermore, we determined that GA treatment increased the active state of PI3K and its downstream protein p-AKT, whereas when using a specific inhibitor of PI3K, Y294002, the levels of p-PI3K and p-AKT decreased. Finally, we showed that GA treatment improved spatial memory and motor coordination in MCAO rats, while TTC staining showed that GA decreased cerebral infarct size in MCAO rats. We reveal that GA protects hippocampal neurons by inhibiting their apoptosis, mainly through the PI3K/AKT signaling pathway.
甘草酸(GA)是甘草中的主要活性物质之一,具有抗炎、抗病毒和神经保护作用。GA可显著减小大脑中动脉闭塞(MCAO)大鼠的脑梗死面积,并抑制炎症反应。然而,GA保护神经元系统的潜在机制仍知之甚少。使用CCK-8和Edu检测法检测细胞增殖和活力。使用流式细胞术和Tunel检测法检测GA对细胞凋亡的影响。进行蛋白质免疫印迹法以评估蛋白质表达。使用莫里斯水迷宫和旋转试验进行行为实验。使用TTC染色观察梗死面积。我们报告称,在氧糖剥夺/复氧(OGD/R)和MCAO大鼠模型中,GA主要通过PI3K/AKT途径抑制细胞凋亡来保护神经元。GA可增加氧糖剥夺的海马神经元的活力和增殖。在体外和体内给予GA处理后,海马神经元凋亡减少。此外,我们确定GA处理可增加PI3K及其下游蛋白p-AKT的活性状态,而当使用PI3K特异性抑制剂Y294002时,p-PI3K和p-AKT的水平降低。最后,我们表明GA处理可改善MCAO大鼠的空间记忆和运动协调能力,而TTC染色显示GA可减小MCAO大鼠的脑梗死面积。我们揭示GA主要通过PI3K/AKT信号通路抑制海马神经元凋亡来保护它们。