Han Zi-Wei, Chang Yue-Chen, Zhou Ying, Zhang Hang, Chen Long, Zhang Yang, Si Jun-Qiang, Li Li
Department of Physiology, Medical College of Shihezi University; Key Laboratory of Xinjiang Endemic and Ethnic Disease, Shihezi University School of Medicine, Shihezi, Xinjiang Uygur Autonomous Region, China.
Key Laboratory of Xinjiang Endemic and Ethnic Disease, Shihezi University School of Medicine, Shihezi, Xinjiang Uygur Autonomous Region; Affiliated Teng Zhou Central People's Hospital, Jining Medical University, Jining, Shandong Province, China.
Neural Regen Res. 2019 Jul;14(7):1221-1229. doi: 10.4103/1673-5374.251571.
Studies have confirmed a strong association between activation of the endoplasmic reticulum stress pathway and cerebral ischemia/reperfusion (I/R) injury. In this study, three key proteins in the endoplasmic reticulum stress pathway (glucose-regulated protein 78, caspase-12, and C/EBP homologous protein) were selected to examine the potential mechanism of endoplasmic reticulum stress in the neuroprotective effect of G protein-coupled estrogen receptor. Female Sprague-Dawley rats received ovariectomy (OVX), and then cerebral I/R rat models (OVX + I/R) were established by middle cerebral artery occlusion. Immediately after I/R, rat models were injected with 100 μg/kg E2 (OVX + I/R + E2), or 100 μg/kg G protein-coupled estrogen receptor agonist G1 (OVX + I/R + G1) in the lateral ventricle. Longa scoring was used to detect neurobehavioral changes in each group. Infarct volumes were measured by 2,3,5-triphenyltetrazolium chloride staining. Morphological changes in neurons were observed by Nissl staining. Terminal dexynucleotidyl transferase-mediated nick end-labeling staining revealed that compared with the OVX + I/R group, neurological function was remarkably improved, infarct volume was reduced, number of normal Nissl bodies was dramatically increased, and number of apoptotic neurons in the hippocampus was decreased after E2 and G1 intervention. To detect the expression and distribution of endoplasmic reticulum stress-related proteins in the endoplasmic reticulum, caspase-12 distribution and expression were detected by immunofluorescence, and mRNA and protein levels of glucose-regulated protein 78, caspase-12, and C/EBP homologous protein were determined by polymerase chain reaction and western blot assay. The results showed that compared with the OVX + I/R group, E2 and G1 treatment obviously decreased mRNA and protein expression levels of glucose-regulated protein 78, C/EBP homologous protein, and caspase-12. However, the G protein-coupled estrogen receptor antagonist G15 (OVX + I/R + E2 + G15) could eliminate the effect of E2 on cerebral I/R injury. These results confirm that E2 and G protein-coupled estrogen receptor can inhibit the expression of endoplasmic reticulum stress-related proteins and neuronal apoptosis in the hippocampus, thereby improving dysfunction caused by cerebral I/R injury. Every experimental protocol was approved by the Institutional Ethics Review Board at the First Affiliated Hospital of Shihezi University School of Medicine, China (approval No. SHZ A2017-171) on February 27, 2017.
研究已证实内质网应激途径的激活与脑缺血/再灌注(I/R)损伤之间存在密切关联。在本研究中,选取内质网应激途径中的三种关键蛋白(葡萄糖调节蛋白78、半胱天冬酶-12和C/EBP同源蛋白),以探讨内质网应激在G蛋白偶联雌激素受体神经保护作用中的潜在机制。对雌性Sprague-Dawley大鼠进行卵巢切除术(OVX),然后通过大脑中动脉闭塞建立脑I/R大鼠模型(OVX + I/R)。I/R后立即向大鼠模型侧脑室内注射100 μg/kg E2(OVX + I/R + E2)或100 μg/kg G蛋白偶联雌激素受体激动剂G1(OVX + I/R + G1)。采用Longa评分检测各组神经行为变化。通过2,3,5-三苯基氯化四氮唑染色测量梗死体积。通过尼氏染色观察神经元的形态变化。末端脱氧核苷酸转移酶介导的缺口末端标记染色显示,与OVX + I/R组相比,E2和G1干预后神经功能明显改善,梗死体积减小,正常尼氏体数量显著增加,海马区凋亡神经元数量减少。为检测内质网中内质网应激相关蛋白的表达和分布,通过免疫荧光检测半胱天冬酶-12的分布和表达,并通过聚合酶链反应和蛋白质印迹法测定葡萄糖调节蛋白78、半胱天冬酶-12和C/EBP同源蛋白的mRNA和蛋白水平。结果显示,与OVX + I/R组相比,E2和G1处理明显降低了葡萄糖调节蛋白78、C/EBP同源蛋白和半胱天冬酶-12的mRNA和蛋白表达水平。然而,G蛋白偶联雌激素受体拮抗剂G15(OVX + I/R + E2 + G15)可消除E2对脑I/R损伤的影响。这些结果证实,E2和G蛋白偶联雌激素受体可抑制海马区内质网应激相关蛋白的表达和神经元凋亡,从而改善脑I/R损伤所致的功能障碍。本研究的每个实验方案均于2017年2月27日获得中国石河子大学医学院第一附属医院机构伦理审查委员会批准(批准号:SHZ A2017-171)。