北方药学
北方藥學
북방약학
JOURNAL OF NORTH PHARMACY
2013年
2期
41
,共1页
吴成举%陈靖%谢鑫%茹东风
吳成舉%陳靖%謝鑫%茹東風
오성거%진정%사흠%여동풍
癫痫%神经元%海马
癲癇%神經元%海馬
전간%신경원%해마
Epilepsy%Neurons%Hippocampal
目的:探讨人参皂苷 Rb1对青霉素所致癫痫大鼠作用.方法:将大鼠随机分为正常(A)组、模型(B)组及人参皂苷 Rb1(C)组.采用青霉素制作癫痫模型制作方法,观察 B 组及 C 组大鼠癫痫发作潜伏期及发作持续时间,并测定各组大鼠海马组织(SOD)、(MDA)含量.结果:C 组大鼠发作潜伏期较 B 组明显延长(P<0.01),发作时间显著缩短(P<0.05). C 组大鼠 SOD 活性与B 组相比显著升高(P<0.01),与 A 组比较明显降低(P<0.05). C 组 MDA 含量与 B 组比较显著降低(P<0.01),与 A 组比较差异无统计学意义(P>0.05).结论:人参皂苷 Rb1可通过抗氧化机制发挥抗癫痫作用.
目的:探討人參皂苷 Rb1對青黴素所緻癲癇大鼠作用.方法:將大鼠隨機分為正常(A)組、模型(B)組及人參皂苷 Rb1(C)組.採用青黴素製作癲癇模型製作方法,觀察 B 組及 C 組大鼠癲癇髮作潛伏期及髮作持續時間,併測定各組大鼠海馬組織(SOD)、(MDA)含量.結果:C 組大鼠髮作潛伏期較 B 組明顯延長(P<0.01),髮作時間顯著縮短(P<0.05). C 組大鼠 SOD 活性與B 組相比顯著升高(P<0.01),與 A 組比較明顯降低(P<0.05). C 組 MDA 含量與 B 組比較顯著降低(P<0.01),與 A 組比較差異無統計學意義(P>0.05).結論:人參皂苷 Rb1可通過抗氧化機製髮揮抗癲癇作用.
목적:탐토인삼조감 Rb1대청매소소치전간대서작용.방법:장대서수궤분위정상(A)조、모형(B)조급인삼조감 Rb1(C)조.채용청매소제작전간모형제작방법,관찰 B 조급 C 조대서전간발작잠복기급발작지속시간,병측정각조대서해마조직(SOD)、(MDA)함량.결과:C 조대서발작잠복기교 B 조명현연장(P<0.01),발작시간현저축단(P<0.05). C 조대서 SOD 활성여B 조상비현저승고(P<0.01),여 A 조비교명현강저(P<0.05). C 조 MDA 함량여 B 조비교현저강저(P<0.01),여 A 조비교차이무통계학의의(P>0.05).결론:인삼조감 Rb1가통과항양화궤제발휘항전간작용.
Objective:To explore ginsenoside Rb1 to penicillin cause epilepsy rat role. Methods: The rats were randomly divided into normal (A) group, model group (B)and ginseng saponin Rb1 (C)group. Using the penicillin production epilepsy model making method, Observe group B and C group of rats epileptic seizure incubation period and the attack last time, And determinate the rat hippocampal tissue(SOD) and(MDA)content.Results:C rats, seizure incubation period was significantly longer than group B(P<0.01). Onset time was significantly shortened(P<0.05). C rats, SOD activity compared with group B significantly increased(P<0.01). And group A comparison decreased obviously (P<0.05). C group of MDA content and group B is significantly reduced (P<0.01). And group A of comparative differences no statistical significance (P>0.05). Conclusions:ginsenoside Rb1 can through the antioxidant mechanism to play antiepileptic effect.