Zhu Shuzhen, Gao Xiaoya, Huang Kaibin, Gu Yong, Hu Yafang, Wu Yongming, Ji Zhong, Wang Qing, Pan Suyue
1Department of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China.
2Department of Neurology, Zhujiang Hospital, Southern Medical University, Guangzhou, Guangdong, China.
Aging Dis. 2018 Aug 1;9(4):685-695. doi: 10.14336/AD.2017.0927. eCollection 2018 Aug.
Glibenclamide (GBC) is an antidiabetic drug that is in a class of medications known as sulfonylureas, which play critical roles in attenuating brain edema and reducing mortality in ischemic stroke patients. Therapeutic hypothermia (TH) is another robust neuroprotectant that prevents brain swelling and improves the neurological outcomes of stroke patients. However, whether the combination of GBC and TH can be used as a reliable neuroprotectant in ischemic stroke remains largely unknown. We used the middle cerebral artery occlusion (MCAO) rat model as well as oxygen and glucose deprivation-reoxygenation (OGD/R) endothelial cells as ischemic stroke models to investigate the efficacy and mechanisms of treating ischemic stroke with the combination of GBC and TH. The serum glucose, mortality rate, neurobehavioral functions, tight junctions, endothelial cells and inflammatory cytokines were evaluated in the stroke models after treatment with GBC, TH or the combination of them. After 5-hour occlusion and subsequent reperfusion, rats exhibited a large volume of hemispheric swelling and a high mortality rate. Stroke rats treated with the combined therapy did not exhibit hypoglycemia. The combination of GBC and TH exhibited synergistic neuroprotective effects in stroke rats that were associated with greater reductions in edema volume, better improvement in neurobehavioral functions, prevention of tight junction loss, and reduction of expression of the inflammatory cytokines COX-2 and iNOS. In OGD/R endothelia cells, the combination reduced endothelial cell death. This study demonstrated that both GBC and TH are neuroprotective after the severe stroke; however, combined therapy with GBC and TH enhanced the efficiency and efficacy of the effects of TH and GBC in the treatment of ischemia. This combined therapy may facilitate the clinical translation of TH management for severe stroke. The combination of GBC and TH seems to be a feasible and promising clinical strategy to alleviate cerebral injury following severe stroke.
格列本脲(GBC)是一种抗糖尿病药物,属于磺脲类药物,这类药物在减轻缺血性中风患者的脑水肿和降低死亡率方面发挥着关键作用。治疗性低温(TH)是另一种强大的神经保护剂,可防止脑部肿胀并改善中风患者的神经功能结局。然而,GBC与TH联合使用是否可作为缺血性中风可靠的神经保护剂在很大程度上仍不清楚。我们使用大脑中动脉闭塞(MCAO)大鼠模型以及氧糖剥夺-复氧(OGD/R)内皮细胞作为缺血性中风模型,来研究GBC与TH联合治疗缺血性中风的疗效和机制。在用GBC、TH或它们的组合治疗后,评估中风模型中的血糖、死亡率、神经行为功能、紧密连接、内皮细胞和炎性细胞因子。在闭塞5小时并随后再灌注后,大鼠出现大量半球肿胀和高死亡率。接受联合治疗的中风大鼠未出现低血糖。GBC与TH的组合在中风大鼠中表现出协同神经保护作用,这与更大程度地减少水肿体积、更好地改善神经行为功能、防止紧密连接丧失以及降低炎性细胞因子COX-2和iNOS的表达有关。在OGD/R内皮细胞中,该组合减少了内皮细胞死亡。本研究表明,GBC和TH在严重中风后均具有神经保护作用;然而,GBC与TH联合治疗提高了TH和GBC在治疗缺血中的效果的效率和效力。这种联合治疗可能有助于将TH管理应用于严重中风的临床转化。GBC与TH的组合似乎是减轻严重中风后脑损伤的一种可行且有前景的临床策略。