Zuo Wei, Zhang Wei, Han Ning, Chen Nai-Hong
State Key Laboratory of Bioactive Substances and Function Natural Medicines, Department of Pharmacology, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Xuanwu District, Beijing, China.
CNS Neurosci Ther. 2015 Mar;21(3):280-8. doi: 10.1111/cns.12364. Epub 2015 Jan 20.
Compound IMM-H004 (7-hydroxy-5-methoxy-4-methyl-3-[4-methylpiperazin-1-yl]-2H-chromen-2-one) is a new synthetic derivative of coumarin, and previous studies showed that it exhibited antioxidant and neuroprotective roles in focal cerebral ischemia. However, we know little about the compound's function in transient global ischemia. This study is to investigate whether compound IMM-H004 can protect against transient global ischemic injury.
Four-vessel occlusion (4VO) rat model was induced for a 20-min occlusion and different times of reperfusion to mimic transient global cerebral ischemia. IMM-H004 (3, 6, 9 mg/kg) or Edaravone (6 mg/kg) was administered after 30 min of reperfusion. Morris water maze tests were used to estimate the ability of spatial learning and memory. Nissl staining, TUNEL assay and Immunoblot for Bax/Bcl-2 and activated caspase-3 were used to detect hippocampal neuron injury. Immunoblot for PSD-95 and synapsin 1, and electron microscopy were used to observe synaptic function.
Compared with vehicle group, IMM-H004 significantly improved the spatial learning performance and exhibited less CA1 neurons loss. The expressions of Bax/Bcl-2 and activated caspase-3 were decreased. IMM-H004 also ameliorated synaptic structure, decreased PSD-95 and increased synapsin 1 expression.
These findings suggested that IMM-H004 exerted neuroprotective role in global ischemia by reducing apoptosis and maintaining the integrity of synaptic structure.
化合物IMM-H004(7-羟基-5-甲氧基-4-甲基-3-[4-甲基哌嗪-1-基]-2H-色原酮-2-酮)是香豆素的一种新型合成衍生物,先前的研究表明它在局灶性脑缺血中具有抗氧化和神经保护作用。然而,我们对该化合物在短暂性全脑缺血中的功能了解甚少。本研究旨在探讨化合物IMM-H004是否能预防短暂性全脑缺血损伤。
采用四动脉闭塞(4VO)大鼠模型,闭塞20分钟并进行不同时间的再灌注,以模拟短暂性全脑缺血。再灌注30分钟后给予IMM-H004(3、6、9毫克/千克)或依达拉奉(6毫克/千克)。采用莫里斯水迷宫试验评估空间学习和记忆能力。用尼氏染色、TUNEL检测以及Bax/Bcl-2和活化的半胱天冬酶-3的免疫印迹法检测海马神经元损伤。用PSD-95和突触素1的免疫印迹法以及电子显微镜观察突触功能。
与溶剂对照组相比,IMM-H004显著改善了空间学习表现,CA1神经元损失较少。Bax/Bcl-2和活化的半胱天冬酶-3的表达降低。IMM-H004还改善了突触结构,降低了PSD-95表达并增加了突触素1的表达。
这些发现表明,IMM-H004通过减少细胞凋亡和维持突触结构的完整性在全脑缺血中发挥神经保护作用。