Xu Li, Song Wen-Ting, Lin Cheng-Ren, Ren Jian-Xun, Liu Jian-Xun, Yao Ming-Jiang, Wang Guang-Rui
Research Center, Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing 100091, China.
Yao Xue Xue Bao. 2012 Jul;47(7):870-7.
The rat model of multi-infarct was adopted in this study to elucidate the protective mechanism of Sailuotong capsule (Sailuotong) in recovery period of multiple cerebral infarction. The effects of Sailuotong on levels of Glu, GABA and the expression of NMDA receptor subtypes including NR1, NR2A and NR2B, were detected. The multi-infarct model rats were established by injecting embolizing microsphere via internal carotid artery, and were given Sailuotong treatment (16.5 and 33.0 mg x kg(-1)) for 60 days. The pathological changes in brain ultrastructure were observed by transmission electron microscope. The levels of Glu and GABA in brain tissue were measured with high performance liquid chromatography. The expression of NMDA receptors including NR1, NR2A and NR2B in neurons was evaluated by immunohistochemical staining. Compared with the sham rats, abnormal changes were observed in ultrastructures of neurons, neuroglia cells and synapses of model rat brains. Moreover, significant decrease of Glu and GABA, as well as the elevated expression of NR1, NR2A and NR2B were detected in brain tissues. Sailuotong (16.5 and 33.0 mg x kg(-1)) could improve ultrastructure of cerebral tissue, facilitate synthesis of Glu and GABA, and down-regulate expression of NR1, NR2A and NR2B in neurons. The results demonstrated that Sailuotong could exert neuroprotective effects to some extent in the recovery phase of multiple cerebral infarction by promoting expression of NMDA receptors and synthesis of Glu and GABA.
本研究采用多梗死大鼠模型,以阐明赛络通胶囊(赛络通)在多发性脑梗死恢复期的保护机制。检测赛络通对谷氨酸(Glu)、γ-氨基丁酸(GABA)水平及N-甲基-D-天冬氨酸受体亚型NR1、NR2A和NR2B表达的影响。通过颈内动脉注射栓塞微球建立多梗死模型大鼠,并给予赛络通治疗(16.5和33.0 mg·kg⁻¹)60天。用透射电子显微镜观察脑超微结构的病理变化。采用高效液相色谱法测定脑组织中Glu和GABA的水平。通过免疫组织化学染色评估神经元中NR1、NR2A和NR2B等N-甲基-D-天冬氨酸受体的表达。与假手术大鼠相比,模型大鼠脑神经元、神经胶质细胞和突触的超微结构出现异常变化。此外,脑组织中Glu和GABA显著降低,NR1、NR2A和NR2B的表达升高。赛络通(16.5和33.0 mg·kg⁻¹)可改善脑组织超微结构,促进Glu和GABA的合成,并下调神经元中NR1、NR2A和NR2B的表达。结果表明,赛络通可通过促进N-甲基-D-天冬氨酸受体表达及Glu和GABA合成,在多发性脑梗死恢复期发挥一定的神经保护作用。