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葛根素对帕金森病大鼠黑质NGF,c-fos,c-jun表达的影响 被引量:2

Effect of Puerarin on the Expressions of NGF,c-fos,c-jun in Substantia Nigra of Parkinson's Rats
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摘要 目的:研究葛根素对6-羟多巴胺(6-OHDA)致帕金森病大鼠黑质神经生长因子(NGF),即刻早期基因(c-fos,c-jun)mRNA表达的影响。方法:建立帕金森病大鼠模型,随机分成6组:正常组、模型组、左旋多巴阳性组及葛根素低、中、高剂量组,并设立正常组。ig给予葛根素20,40,80 mg.kg-1,阳性组给予左旋多巴40 mg.kg-1,连续灌胃30 d。Nissl染色观察黑质神经细胞尼氏小体的变化,免疫组织化学法检测黑质组织神经生长因子(NGF)表达。原位杂交法检测c-fos,c-jun mRNA表达。结果:与正常组比较,模型组帕金森病大鼠黑质神经细胞严重损伤以及NGF,c-fos,c-jun表达明显减少(P<0.01)。与模型组比较,葛根素有效地增加黑质组织神经细胞尼氏小体数量。增加黑质组织中NGF阳性细胞数量(139.1±26.5),(206.1±33.8),(294.6±40.7)cell.mm-2(P<0.01)。同时明显上调c-fos,c-jun mRNA表达(98.5±16.4),(137.6±19.5),(205.4±28.9);(90.6±15.3),(125.9±18.6),(191.7±27.5)cell.mm-2(P<0.01)。结论:葛根素对6-OHDA所致PD大鼠黑质具有神经保护作用,机制可能与其调节c-fos/c-jun表达而介导神经修复和增强信号传导有关。 Objective: To investigate the effect of puerarin on the expressions of nerve growth factor (NGF) , c-fos, c-jun in substantia nigra of Parkinson's rats induced by 6-hydroxydopamine (6-OHDA). Method: Parkinson's rat model was established, model rats were randomly divided into 5 groups: model group, L-dopa group (40 mg .kg-1 ) , low-, medium-and high-dosage groups of puerarin (20, 40, 80 mg kg-1 ). The drugs were intragastrically perfused to rats daily for 30 days. The changes of nissl bodies in nerve cells of substantia nigra were observed by Nissl staining. The expression of NGF was tested by immunohistochemistry assay. And the c-fos, c-jun mRNA levels were tested by in situ hybridization analysis. Result: Compared to model group, the neuronal cells were badly injured and expression of NGF, c-fos, c-jun mRNA was obviously reduced in substantia nigra of PD rats in model group. Compared to model group, puerarin effectively increased nissl bodies in neuronal cells of substantia nigra of PD rats, and elevated the number of NGF-immunoreactive cells in substantia nigra (P 〈 0.01 ). The expressions of c-fos, c-jun mRNA were significantly up-regulated. Conclusion: The results demonstrate that puerarin has a neuroprotection on the neuronal cells in substantia nigra of PD rats induced by 6-OHDA, though the underlying mechanisms that may be associated with regulation of c-fos/c-jun expressions to mediate neuronic repairment and enhance the signaling transduction.
出处 《中国实验方剂学杂志》 CAS 北大核心 2013年第4期259-262,共4页 Chinese Journal of Experimental Traditional Medical Formulae
关键词 葛根素 6-羟多巴胺 帕金森病 神经修复 信号传导 puerarin 6-hydroxydopamine Parkinson's disease neuronie repairment signalingtransduction
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  • 1沈炳权,蔡兆斌,徐群红,王万铁,宋张娟.葛根素对家兔心肌缺血-再灌注损伤的保护作用[J].中国中西医结合急救杂志,2004,11(6):361-363. 被引量:27
  • 2刘小光,徐理纳.一种能评价溶拴和抗栓药的大鼠大脑中动脉血栓模型[J].药学学报,1995,30(9):662-667. 被引量:103
  • 3邵宴平 焦守恕 等.脑细胞悬液移植治疗黑质损伤-1.黑质损伤动物模型的建立[J].北京第二医学院学报,1986,7:107-107. 被引量:5
  • 4Qin F, Huang X, Zhang H M, et al. Pharmacokinetic comparison of puerarin after oral administration of Jiawei-Xiaoyao-San in healthy volunteers and functional dyspepsia patients: influence of disease state [ J ]. J Pharm Pharmacol,2009,61 ( 1 ): 125. 被引量:1
  • 5Qin F, Liu Y X, Zhao H W, et al. Chinese medicinal formula Guan-Xin-Er-Hao protects the heart against oxidative stress induced by acute ischemic myocardial injury in rats [ J ]. Phytomedicine ,2009,16 ( 2/3 ) :215. 被引量:1
  • 6Prasad A, Stone G W, Holmes D R, et al. Reperfusion injury, microvascular dysfunction, and cardioprotection: the 'dark side' of reperfusion [ J ]. Circulation, 2009, 120 (21) :2105. 被引量:1
  • 7Els-sser A,Suzuki K, Lorenz-Meyer S,et al. The role of apoptosis in myocardial ischemia: a critical appraisal [ J]. Basic Res Cardiol,2001,96 (3) :219. 被引量:1
  • 8Kehrer J P. Cause-effect of oxidative stress and apoptosis [J]. Teratology, 2000,62 (4) :235. 被引量:1
  • 9Zhao Z Q. Oxidative stress-elicited myocardial apoptosis duringreperfusion [ J ]. Curr Opin Pharmacol, 2004, 4(2) :159. 被引量:1
  • 10Wattanapitayakul S K,Bauer J A. Oxidative pathways in cardiovascular disease: roles, mechanisms, and therapeutic implications [ J ]. Pharmacol Ther, 2001,89 (2) :187. 被引量:1

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