首页 | 本学科首页   官方微博 | 高级检索  
     

救脑宁注射液对培养神经细胞缺氧缺糖损伤的保护作用
引用本文:黄世敬,黄启福,孙塑伦,王蕴红. 救脑宁注射液对培养神经细胞缺氧缺糖损伤的保护作用[J]. 北京中医药大学学报, 2001, 24(1): 28-31
作者姓名:黄世敬  黄启福  孙塑伦  王蕴红
作者单位:1. 北京中医药大学病理教研室
2. 国家中医药管理局医政司
基金项目:“九五”国家科技攻关资助课题 !(No .96 90 6 0 6 0 3)
摘    要:为了探索“救脑宁”注射液对中风病的疗效机理 ,将原代培养 8~ 12d的新生大鼠皮层神经细胞进行缺氧缺糖处理 ,观察该药对缺氧缺糖损伤神经细胞的影响。结果表明 :缺氧缺糖组细胞上清液中丙二醛 (MDA)含量、乳酸脱氢酶 (LDH)活性较对照组显著升高 ,细胞超氧化物岐化酶 (SOD)活性和细胞生存率则显著降低 ,救脑宁组MDA、LDH显著低于缺氧缺糖组 ,而SOD活性及细胞生存率则高于缺氧缺糖组 (P <0 0 1)。因此 ,抗脂质过氧化损伤、提高神经细胞对缺氧缺糖的耐受性 ,可能是其疗效机理之一。

关 键 词:救脑宁注射液  缺氧缺糖  神经细胞  乳酸脱氢酶  脂质氧化
修稿时间:1999-09-13

Protective Effects of Jiunaoning Injection against the Lesions of Cultured Nerve Cells Caused by Oxygen and Glucose Deprivation
Huang Shijing,Huang Qifu,Sun Sulun,et al.. Protective Effects of Jiunaoning Injection against the Lesions of Cultured Nerve Cells Caused by Oxygen and Glucose Deprivation[J]. Journal of Beijing University of Traditional Chinese Medicine, 2001, 24(1): 28-31
Authors:Huang Shijing  Huang Qifu  Sun Sulun  et al.
Abstract:The cortical cells of the new-born rat cultured for 8~12 days by the primary culture method were treated by oxygen and glucose deprivation (OGD), an d the effects of Jiunaoning Injection (JI) on the OGD-injured cortical cells we r e observed. The results showed that the MDA level and the LDH activity in the ce ll supernate were significantly increased, while the SOD activity and cell survi val rate were significantly decreased in the OGD group, compared with those in t h e control group; and the MDA level and the LDH activity were significantly decre ased, while the SOD activity and cell survival rate were increased in the JI gro up, compared with those in the OGD group. The results suggest that the basis of t he clinical effects of JI is relieving the lesions caused by lipid peroxidation and increasing the tolerance of nerve cells to OGD.
Keywords:Jiunaoning Injection  Oxygen and Glucose Deprivation  Nerve Cell  Lactic Dehydrogenase  Lipid Oxidation
本文献已被 CNKI 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号