Fu Kun, Chen Liqiang, Hu Shuai, Guo Yan, Zhang Wei, Bai Yunan
Department of Neurosurgery, Yidu Central Hospital of Weifang, No 4138 Linglongshan Road, Qingzhou, 262500, Shandong, China.
Department of Neurology, Qingdao West Coast New Area Central Hospital, Qingdao, 266000, Shandong, China.
Acta Neurol Belg. 2021 Apr;121(2):357-364. doi: 10.1007/s13760-019-01111-9. Epub 2019 Mar 5.
Grape seed proanthocyanidins (GSP) has been reported to attenuate endoplasmic reticulum (ER) stress-induced apoptosis, which is associated with ischemic stroke. However, whether GSP pays crucial roles in ischemic stroke still remains unclear. The purpose of this study is to explore the role of GSP in ischemic stroke and the underlying mechanism. The ischemic stroke mouse model was established by middle cerebral artery occlusion. GSP administration was performed intragastrically. Long-term neurological outcome was assessed by the foot fault test after reperfusion. Brain injury was identified by infarct volume from 2,3,5-triphenyltetrazolium chloride staining. Neuronal apoptosis was detected by terminal deoxynucleotidyl transferase dUTP nick end labeling. The expression levels of Bax, Bcl-2, Cleaved Caspase-3, phosphorylated ERK (p-ERK), ERK, Glucose-regulated protein 78 kDa (GRP78), Caspase-12 were detected by western blotting. In mice with ischemia stroke, GSP administration improved long-term neurological outcomes by attenuating ischemia-reperfusion induced neuronal apoptosis and brain injury. Mechanically, GSP performance inhibited the expression levels of ER stress-associated genes. GSP protects mice against ischemic stroke via attenuating neuronal apoptosis. Moreover, GSP attenuated ER stress-associated apoptosis by inhibiting GRP78 and Caspase-12. Our study indicates that GSP attenuates neuronal apoptosis in ischemic stroke, which shows the potential for ischemic stroke treatment.
据报道,葡萄籽原花青素(GSP)可减轻内质网(ER)应激诱导的细胞凋亡,这与缺血性中风有关。然而,GSP在缺血性中风中是否起关键作用仍不清楚。本研究的目的是探讨GSP在缺血性中风中的作用及其潜在机制。通过大脑中动脉闭塞建立缺血性中风小鼠模型。通过胃内给予GSP。再灌注后通过足错试验评估长期神经功能结局。通过2,3,5-三苯基四氮唑氯化物染色的梗死体积确定脑损伤。通过末端脱氧核苷酸转移酶dUTP缺口末端标记检测神经元凋亡。通过蛋白质印迹法检测Bax、Bcl-2、裂解的半胱天冬酶-3、磷酸化的ERK(p-ERK)、ERK、葡萄糖调节蛋白78 kDa(GRP78)、半胱天冬酶-12的表达水平。在缺血性中风小鼠中,给予GSP可通过减轻缺血再灌注诱导的神经元凋亡和脑损伤来改善长期神经功能结局。从机制上讲,GSP的作用抑制了内质网应激相关基因的表达水平。GSP通过减轻神经元凋亡保护小鼠免受缺血性中风的影响。此外,GSP通过抑制GRP78和半胱天冬酶-12减轻内质网应激相关的细胞凋亡。我们的研究表明,GSP可减轻缺血性中风中的神经元凋亡,这显示了其在缺血性中风治疗中的潜力。