Zhang Huinan, Meng Jingru, Li Xubo, Zhou Shimeng, Qu Di, Wang Ning, Jia Min, Ma Xue, Luo Xiaoxing
Department of Pharmacology, School of Pharmacy, The Fourth Military Medical University, Xi'an, China.
Department of Pharmacology, School of Pharmacy, The Fourth Military Medical University, Xi'an, China.
Eur J Pharm Sci. 2015 Apr 5;70:82-91. doi: 10.1016/j.ejps.2015.01.010. Epub 2015 Jan 30.
Pro-Glucagon-like peptide-1 (Pro-GLP-1), a long-lasting GLP-1 receptor (GLP-1R) agonist, was developed using a polymeric pro-drug strategy and its neuroprotective effects on ischemic stroke were investigated in C57BL/6 mice. Pro-GLP-1 was injected into the intraperitoneal cavity of C57BL/6 mice once a day for 7days before middle cerebral artery occlusion (MCAO) surgery. The neurological deficit score and TTC staining were determined 24h after ischemia. The results demonstrated that Pro-GLP-1 was slowly degraded in the plasma and brain of the mice, and GLP-1 could be detected even 12h after administration. Pro-GLP-1 was significantly neuroprotective in C57BL/6 mice subjected to MCAO. In cultured cortical neurons, treatment with Pro-GLP-1 attenuated apoptosis induced by oxygen-glucose deprivation (OGD). The neuroprotective effects of Pro-GLP-1 were blocked by a selective GLP-1 receptor antagonist and knockdown of GLP-1 receptor with shRNA. However, Pro-GLP-1 had no effect on blood glucose and insulin levels which indicated that neuroprotection was mediated by the activation of GLP-1 receptor in the brain. Pro-GLP-1 repaired the balance of pro- and anti-apoptotic proteins and decreased the expression of caspase-3. The anti-apoptotic effect was mediated by the cAMP/PKA and PI3K/Akt pathway. Our research provides evidence that pre-treatment of MCAO mice with Pro-GLP-1 exerts a neuroprotective effect mediated by a blockade of apoptosis and that Pro-GLP-1 might be a potential neuroprotective agent candidate against ischemic stroke.
前胰高血糖素样肽-1(Pro-GLP-1)是一种长效胰高血糖素样肽-1受体(GLP-1R)激动剂,采用聚合物前药策略研发,并在C57BL/6小鼠中研究了其对缺血性中风的神经保护作用。在大脑中动脉闭塞(MCAO)手术前7天,每天向C57BL/6小鼠腹腔注射一次Pro-GLP-1。缺血24小时后测定神经功能缺损评分和TTC染色。结果表明,Pro-GLP-1在小鼠血浆和脑中缓慢降解,给药后12小时仍能检测到GLP-1。Pro-GLP-1对接受MCAO的C57BL/6小鼠具有显著的神经保护作用。在培养的皮质神经元中,Pro-GLP-1处理可减轻氧糖剥夺(OGD)诱导的细胞凋亡。Pro-GLP-1的神经保护作用被选择性GLP-1受体拮抗剂和用shRNA敲低GLP-1受体所阻断。然而,Pro-GLP-1对血糖和胰岛素水平没有影响,这表明神经保护作用是由大脑中GLP-1受体的激活介导的。Pro-GLP-1修复了促凋亡蛋白和抗凋亡蛋白的平衡,并降低了caspase-3的表达。抗凋亡作用由cAMP/PKA和PI3K/Akt途径介导。我们的研究提供了证据,即Pro-GLP-1预处理MCAO小鼠可通过阻断细胞凋亡发挥神经保护作用,并且Pro-GLP-1可能是一种潜在的抗缺血性中风神经保护剂候选药物。