Meng Fanrui, Wang Yuehua, Liu Rui, Gao Mei, DU Guanhua
College of Pharmacy, Liaoning University, Shenyang, Liaoning 110036, P.R. China ; National Center for Pharmaceutical Screening, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, P.R. China.
National Center for Pharmaceutical Screening, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, P.R. China.
Exp Ther Med. 2014 Oct;8(4):1285-1290. doi: 10.3892/etm.2014.1923. Epub 2014 Aug 19.
The aim of the present study was to investigate the effect of pinocembrin on cognitive ability impairment in a rat model of transient global cerebral ischemia (TGCI). The TGCI model was established by inducing global cerebral ischemia for 20 min, followed by reperfusion for two weeks. The rats were divided into five experimental groups, including the sham group that were not subjected to ischemia, and four ischemic groups where the rats were exposed to TGCI. The sham and control TGCI groups were administered a vehicle intravenously immediately after reperfusion, while the other three groups were intravenously treated with 1, 5 and 10 mg/kg pinocembrin, respectively. In the present study, neurological scores were analyzed at 0 and 24 h after reperfusion, and the effect of pinocembrin on cognitive ability impairment in the TGCI rat model was investigated using a Morris water maze test. Neuronal loss was observed under an optical microscope with the assistance of Nissl staining. In addition, glial fibrillary acidic protein (GFAP)-positive cells were observed under an optical microscope by an immunohistochemistry assay. Pinocembrin treatment was found to alleviate the cognitive impairments, decrease the neurological scores, diminish neuronal loss in the hippocampus and reduce the number of GFAP-positive cells in the hippocampal CA1 region of the TGCI rats. Therefore, pinocembrin alleviated memory impairment in the TGCI rats.
本研究的目的是探讨白杨素对短暂性全脑缺血(TGCI)大鼠模型认知能力损害的影响。通过诱导全脑缺血20分钟,随后再灌注两周来建立TGCI模型。将大鼠分为五个实验组,包括未经历缺血的假手术组,以及四个经历TGCI的缺血组。假手术组和对照TGCI组在再灌注后立即静脉注射赋形剂,而其他三组分别静脉注射1、5和10mg/kg白杨素。在本研究中,在再灌注后0和24小时分析神经学评分,并使用Morris水迷宫试验研究白杨素对TGCI大鼠模型认知能力损害的影响。在尼氏染色的辅助下,在光学显微镜下观察神经元丢失。此外,通过免疫组织化学分析在光学显微镜下观察胶质纤维酸性蛋白(GFAP)阳性细胞。发现白杨素治疗可减轻认知障碍,降低神经学评分,减少海马神经元丢失,并减少TGCI大鼠海马CA1区GFAP阳性细胞的数量。因此,白杨素减轻了TGCI大鼠的记忆障碍。