期刊文献+

复方人参健脑液对大鼠缺血再灌注脑细胞损伤的作用 被引量:2

Compound Ginseng Brain Tonic Liquid on Cerebral Ischemiareperfusion Injury in Rats
原文传递
导出
摘要 目的:观察复方人参健脑液对脑缺血再灌注损伤的保护作用。方法:大鼠随机分为正常对照组,脑缺血再灌注模型组,复方人参健脑液高剂量组(10 g.kg-1),复方人参健脑液低剂量(5 g.kg-1),维生素E组(1 g.kg-1)。采用颈动脉结扎法构建大鼠脑缺血再灌注损伤模型,硫代巴比妥酸法测定脑细胞脂质过氧化物含量,比色法测定还原型谷胱甘肽含量,氧电极法测定脑细胞耗氧量。结果:模型组大鼠脑脂质过氧化物含量明显增加(P<0.001),还原型谷胱甘肽含量减少(P<0.001),脑细胞耗氧量增加(P<0.01)。复方人参健脑液高剂量、低剂量组与模型组比较,脑脂质过氧化物水平降低(P<0.001),还原型谷胱甘肽含量增加(P<0.001),脑细胞耗氧量减少(P<0.001)。结论:复方人参健脑液对脑缺血再灌注损伤有一定的保护作用。 Objective: To study the effect of Compound Ginseng Brain Tonic Liquid (CGBTL) on cerebral ischemia-reperfusion injury. Method: Rats were randomly divided into normal control group, cerebral ischemia and reperfusion model group, large drug dose + model group ( CGBTL 10 g·kg-1) , small drug dose + model group ( CGBTL 5 g ·kg-1) , vitamin E + model group. The model of cerebral ischemia reperfusion rats was established by ligaturing carotid. The lipid peroxide content of brain cell was measured with thiobarbituric acid. Reduced glutathione was determined by the method of spectrophotometer. Oxygen consumption was measured with clark oxygen electrode method. Result: In rats with cerebral ischemia-reperfusion injury, there showed an increase in lipid peroxide content (P〈 0. 001 ), a decrease in reduced glutathione (P 〈 0. 001 ) and an increase in oxygen Consumption (P 〈0. 001 ) compared with those in the normal control group. In CGBTL large dose and small dose groups, compared with the model group, there showed a decrease in lipid peroxide content (P 〈 0. 001 ) , and an increase in reduced glutathione content (P 〈 0. 001 ) and a decrease in oxygen consumption (P 〈 0. 001 ). In vitamin E treatment group, the outcomes were significant (P 〈 0. 001 ). Conclusion : CGBTL has preventive effect on cerebral ischemia-reperfusion injury.
出处 《中国实验方剂学杂志》 CAS 北大核心 2012年第17期208-211,共4页 Chinese Journal of Experimental Traditional Medical Formulae
关键词 复方人参健脑液 脑缺血再灌注 脂质过氧化物 还原型谷胱甘肽 脑细胞耗氧 Compound Ginseng Brain Tonic Liquid cerebral ischemia-reperfusion lipid peroxidation reduced glutathione oxygen consumption
  • 相关文献

参考文献7

二级参考文献30

  • 1田恒力,张镛.一氧化氮生物作用的研究进展[J].国外医学(神经病学.神经外科学分册),1995,22(2):87-90. 被引量:38
  • 2孟刚 马毅 陈志武.芸香甙对小鼠脑缺血的保护作用[J].中国药理学通报,1996,12:9-9.
  • 3LuXY.Effectofd-catechinonmitochondriainjuryinratliverinducedbyascorbateandFeSO4.ActaBiophysSin(生物物理学报),1997,13(1):35-35.
  • 4Yong. W. Hary R, David J. Regional brain Sodium, potassium and water changes in the rat middle cerebral artery occlusion model of ischemia.[J] Stroke, 1987, 18:751-9.
  • 5Geetha A, Parameswari S. Effect of ursodeoxycholic acid on hydrogen peroxide induced lipid peroxidation in sheep liver mitochondria [ J ]. Indian J Physiol Pharmacol,2002,46 (3): 343 - 348.
  • 6Kaur J, Sharma D, Singh R. Acetyl-L-carnitine enhances Na+, K+-ATPase glutathione-s-transferase and multiple unit activity and reduces lipid peroxidation and lipofuscin concentration in aged rat brain regions [ J ]. Neurosci Lett, 2001,301(1) :1 -4.
  • 7Kaur J, Sharma D, Singh R. Regional effects of ageing on Na+, K+-ATPase activity in rat brain and correlation with multiple unit action potentials and lipid peroxidation[J]. Indian J Biochem Biophys, 1998,35(6):364 -367.
  • 8Chakraborty H, Sen P, Sur A, et al. Age-related oxidative inactivation of Na+, K+-ATPase in rat brain crude synaptosomes [ J ]. Exp Gerontol, 2003,38 ( 6 ): 705.
  • 9Lehotsky J, Kaplan P, Matejovicova M, et al. Ion transport systems as targets of free radicals during ischemia reperfusion injury [J]. Gen Physiol Biophys,2002,21(1) :31 -37.
  • 10Miyakae H, Kadoya A, Ohyashiki T. Increase in molecular rigidity of the protein conformation of brain Na +, K +-ATPase by modification with 4-hydroxy-2-nonenal[J]. Biol Pharm Bull, 2002,26(12) :1652.

共引文献185

同被引文献40

  • 1张梅,高吉国,赵腾,张蓓琳,刘雁伟,周春奎.MCP-1与血管性痴呆[J].中国老年学杂志,2014,34(6):1728-1730. 被引量:3
  • 2胡琴,陈春花,杨晓梅,杨磊,王珂,韩晶岩,周长满.养血清脑颗粒对蒙古沙鼠全脑缺血再灌注后海马CA1区神经元的治疗作用[J].解剖学报,2007,38(5):520-524. 被引量:10
  • 3Goldberg TH,Griffith JP. Can Alzheimer's or vascular demen- tia be prevented with control of vascular risk factors [J]. W V Med J,2011,107(3) :20-25.
  • 4Black SE. Vascular cognitive impairment:epidemiology, subtypes,diagnosis and management [J]. J R Coll Physicians Edinb,2011,41 (1) :49-56.
  • 5Maki T, Ihara M, Fujita Y, et al. Angiogenic and vasoprotec- tive effects of adrenomedullin on prevention of cognitive decline after chronic cerebral hypoperfusion in mice [J]. Stroke,2011,4(42) : 1122-1128.
  • 6Dong YF, Kataoka K,Toyama K, et al. Attenuation of brain damage and cognitive impairment by direct renin inhibi- tion in mice with chronic cerebral hypoperfusion [J]. Hyper-tension, 2011,10 (58) : 635 -642.
  • 7Oades R, Taghzouti K, Simon H, et al. Dopamine-sensitive alternation and collateral behavior in a Y-maze:effects of d-amphetamine and haloperidol [J]. Psychopharmacology (Berl), 1985,85 ( 1 ) : 123 - 128.
  • 8Hermann GE, Viard E, Rogers RC. Hindbrain glucopriva- tion effects on gastric vagal reflex circuits and gastric motility in the rat are suppressed by the astrocyte in- hibitor fluorocitrate [J]. J Neurosci, 2014,34 (32) : 10488- 10496.
  • 9Janae B,Radenovie L,Selakovie V,et al. Time course of motor behavior changes in Mongolian gerbils submitted to different durations of cerebral isehemia [J]. Behav Brain Res,2006,175(2) :362-373.
  • 10Li H,Park JH,Yan B,et al. Neuroprotection of alpinia katsumadai seed extract against neuronal damage in the isehemie gerbil hippocampus is linked to altered brain- derived neurotrophic factor [J]. Lab Anim Res, 2011,27 (1):67-71.

引证文献2

二级引证文献10

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部