曲玲, 王维亭, 郭莲军, 王芳, 吕青, 钱家庆. DDPH对大鼠缺血性脑损伤的保护作用J. 药学学报, 2003, 38(10): 725-727.
引用本文: 曲玲, 王维亭, 郭莲军, 王芳, 吕青, 钱家庆. DDPH对大鼠缺血性脑损伤的保护作用J. 药学学报, 2003, 38(10): 725-727.
QU Ling, WANG Wei-ting, GUO Lian-jun, Lü Qing, QIAN Jia-qing, . Protective effects of 1-(2,6-dimethylphenoxy)-2-(3,4-dimethoxy-phenylethylamino)propane hydrochloride(DDPH)on brain ischemia injury in ratsJ. Acta Pharmaceutica Sinica, 2003, 38(10): 725-727.
Citation: QU Ling, WANG Wei-ting, GUO Lian-jun, Lü Qing, QIAN Jia-qing, . Protective effects of 1-(2,6-dimethylphenoxy)-2-(3,4-dimethoxy-phenylethylamino)propane hydrochloride(DDPH)on brain ischemia injury in ratsJ. Acta Pharmaceutica Sinica, 2003, 38(10): 725-727.

DDPH对大鼠缺血性脑损伤的保护作用

Protective effects of 1-(2,6-dimethylphenoxy)-2-(3,4-dimethoxy-phenylethylamino)propane hydrochloride(DDPH)on brain ischemia injury in rats

  • 摘要: 目的研究DDPH对大鼠缺血性脑损伤的保护作用,并初步探讨其作用机制。方法用线拴法制备大鼠局灶性脑缺血模型,观察DDPH对大鼠脑缺血后神经症状、梗死面积的影响;用大鼠弥漫性不完全性脑缺血模型,观察DDPH对脑缺血后脑组织超氧化物歧化酶(SOD)活性、丙二醛(MDA)含量及组织病理损伤的影响。结果DDPH 10 mg·kg-1在缺血前30 min ip,局灶性脑缺血模型大鼠在3 h后神经症状明显改善,24 h梗死面积缩小。DDPH使大鼠弥漫性不完全性脑缺血后脑组织内SOD活性增高,MDA含量下降,并明显改善神经细胞的病理性损伤。 结论 DDPH对大鼠缺血性脑损伤有一定保护作用,其机制可能与阻滞钙离子通道、提高SOD活性有关。

     

    Abstract: AimTo study the effects of 1-(2,6-dimethylphenoxy)-2-(3,4-dimethoxyphenylethylamino) propane hydrochloride(DDPH) on brain ischemia injury in rats. MethodsBy using the middle cerebral artery occlusion (MCAO) induced by nylon surgical thread inserted through the internal carotid artery into the anterior cerebral artery in rats, the effects of DDPH on neuron defects(ND) and infarct size(IS)were investigated.Using incomplete cerebral ischemia in rats, the effects of DDPH on superoxide dismutase(SOD) activity and malondialdehyde (MDA) content in brain tissue and pathological changes in rats were studied.ResultsDDPH at the dose of 10 mg·kg-1 ip 30 min before ischemia decreased the ND 3 h after ischemia.The IS declined 24 h after ischemia as well.Meanwhile, DDPH was found to increase SOD activity and reduce the MDA content, as well as mitigate pathological damage of neuron after brain ischemia in rats.ConclusionDDPH showed protective effects on brain ischemia, probably related to its properties of calcium antagonistic effect and increasing the activity of superoxide dismutases.

     

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