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依达拉奉对癫痫大鼠海马硫氧还蛋白还原酶活性影响的研究

Study on Effects of Edaravone on Thioredoxin Reductase Activity in Hippocampus of rats with Seizure
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摘要 目的研究依达拉奉(Ed)对海人酸(KA)诱导癫痫大鼠海马组织硫氧还蛋白还原酶(TrxR)活性的影响。方法 SD大鼠随机分为癫痫对照组(saline组)、癫痫组(KA组)和药物对照组(KA+saline组)及药物组(Ed+KA组)。采用脑室注射KA制作大鼠癫痫模型,Ed于KA注射前40 min腹腔用药。KA注射6h取海马组织匀浆,应用DTNB还原法对海马TrxR活性进行测定,用Western blot法检测cleaved caspase-3的表达。结果 Saline组、KA组、KA+saline组、Ed+KA组TrxR活性分别为(U/mg protein):66±18、111±42、102±40、75±12;KA组和KA+saline组cleaved caspase-3的表达均较saline组增加(均P<0.05),而Ed+KA组较KA+saline组则降低(P<0.05)。结论 KA诱导癫痫大鼠海马组织TrxR活性增加,依达拉奉可能通过抑制TrxR的活性以增加对神经元的保护作用。 Objective To study the effect of edaravone on thioredoxin reductase(TrxR) activity of hippocampus in rats with seizure induced by kainic acid(KA).Methods Adult male Sprague-Dawley rats weighing 200 to 300g were randomly divided into 4 groups: the control group(saline group),the seizure group(KA group),the vehicle treatment group(KA+saline group) and the edaravone treatment group(Ed+KA group).Seizures were induced by intracerebroventricular injection of KA dissolved in sterile saline.Edaravone was intraperitoneally administrated to the rats 40 min before KA injection.TrxR activity was detected by dithio-bis-nitrobenzoic acid(DTNB) reduction assay.Western blot was used to analyze the expression of cleaved caspase-3.Results Thioredoxin reductase activity(U/mg protein)was 66±18,111±42,102±40 and 75±12.Compared with the saline group,the expression of cleaved caspase-3 increased significantly in the KA group and the KA+saline group(P0.05).Compared with the KA group and the KA+saline group,the expression of cleaved caspase-3 decreased significantly in the Ed+KA group(P0.05).Conclusion TrxR activity increased in hippocampus of rats with seizure induced by KA.Edaravone may exert its neuroprotective effect by inhibiting the increasing of thioredoxin reductase activity.
出处 《苏州大学学报(医学版)》 CAS 北大核心 2011年第5期740-742,805,共4页 Suzhou University Journal of Medical Science
基金 徐州市科技发展项目(XF10C058)
关键词 依达拉奉 癫痫 海人酸 硫氧还蛋白还原酶 caspase-3 edaravone seizure kainic acid thioredoxin reductase caspase-3
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参考文献15

  • 1吴逊.癫痫和发作性疾病[M].北京:人民军医出版社,2001.110.
  • 2Costello D J, Delanty N. Oxidative injury in epilepsy: po- tential for antioxidant therapy [ J ]. Expert Rev Neurother, 2004,4 ( 3 ):541 -553.
  • 3Yamawaki H, Berk BC. Thioredoxin: a mulitifunctional an- tioxidant enzyme in kidney, heart and vessels [ J ]. Curr Opin Nephrol Hypertens, 2005,14 (2) : 149 - 153.
  • 4Miyamoto R, Shimakawa S, Suzuki S,et al. Edaravone pre- vents kainic acid-induced neuronal death [ J]. Brain Res, 2008 (1209) :85-91.
  • 5Racine RJ. Modification of seizure activity by electrical stimulation Ⅱ motor seizure [ J ]. Electroencephaloge Clin Neurophysiol, 1972,32 ( 3 ) : 281 - 294.
  • 6Holmgren A, Bj6mstedt M. Thioredoxin and thioredoxin re- ductase [ J]. Method Enzymol, 1995,252 : 199 - 208.
  • 7Wang Q, Yu S, Simonyi A, et al. Kainic acid-mediated excitotoxicity as a model for neurodegeneration [ J ]. Mol Neurobio1,2005,31 ( 1/2/3 ) :3 - 16.
  • 8Cross DJ, Cavazos JE. Synaptic reorganization in subiculum and CA3 after early-life status epilepticus in the kainic acid rat model [J]. Epilepsy Res,2007,73(2) :156.
  • 9Liu XM, Pei DS, Guan QH, et al. Neuroprotection of Tat- GluR6-9c against neuronal death induced by kainate in rat hippocampus via nuclear and non-nuclear pathways [ J ]. J Biol Chem,2006,281 (25) : 17432 - 17445.
  • 10彭薇,周菊,龚珊,单立冬,蒋星红.caspase-3在海马损伤后齿状回神经发生调控中的作用[J].苏州大学学报(医学版),2009,29(1):82-84. 被引量:2

二级参考文献10

  • 1陈琳,龚珊,单立冬,蒋星红.单侧海马损毁诱发双侧齿状回细胞增殖的研究[J].苏州大学学报(医学版),2005,25(3):362-365. 被引量:6
  • 2Kempermann G, Kuhn HG, Gage FH. Experience-induced neurogenesis in the senescent dentate gyms[J]. J Neurosci,1998,18(9):3206-3212.
  • 3Gould E,Gross CG. Neurogenesis in adult mammals:some progress and problem[J]. J Neurosci, 2002,22(3):619-623.
  • 4West M, Slomianka L, Gundersen H. Unbiased stereological estimation of the total number of neurons in the subdivision of the rat hippocampus using the optical fractionator [J]. Anat Rec, 1991, 231(4):482- 497.
  • 5Hagihara H, Hara M, Tsunekawa K, et al. Tonic-clonic seizures induce division of neuronal progenitor cells with concomitant changes in expression of neurotrophic factors in the brain of pilocarpine-treated mice[J]. Brain Res Mol Brain Bes,2005,139(2):258-266.
  • 6Schlett K. Glutamate as a modulator of embryonic and adult neurogenesis[J]. Curr Top Med Chem, 2006,6(10): 949-960.
  • 7Radley J J, Jaeobs BL. Pilocarpine-induced status epilepti-cus increases cell proliferation in the dentate gyrus of adult rats via a 5-HT1A receptor-dependent mechanism [J]. Brain Res, 2003, 966(1): 1-12.
  • 8Ceceatelli S, Tamm C, Sleeper E, et al. Neural stem cells and cell death[J]. Toxicol Lett, 2004, 149(1-3):59-66.
  • 9Wang Y, Han R, Liang ZQ, et al. An autophagic mecha-nism is involved in apoptotic death of rat stfiatal neurons indued by the non-N-methyl-D-aspartate receptor agonist kainic acid[J]. Autophagy,2008,4(2):214-226.
  • 10Li J, Spletter ML, Johnson DA, et al. Rotenone-induced easpase 9/3-independent and dependent cell death in un-differentiated and differentiated human neural stem cells [J]. J Neurochem, 2005, 92(3):462-476.

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