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Intrastriatal glial cell line-derived neurotrophic factors for protecting dopaminergic neurons in the substantia nigra of mice with Parkinson disease 被引量:4
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作者 Chenghua Xiao Yanqiang Wang +3 位作者 Hongmei Liu Hongjun Wang Junping Cao Dianshuai Gao 《Neural Regeneration Research》 SCIE CAS CSCD 2007年第4期207-210,共4页
BACKGROUND: Substantia nigra is deep in position and limited in range, the glial cell line-derived neurotrophic factor (GDNF) injection directly into substantia nigra has relatively greater damages with higher diff... BACKGROUND: Substantia nigra is deep in position and limited in range, the glial cell line-derived neurotrophic factor (GDNF) injection directly into substantia nigra has relatively greater damages with higher difficulty. GDNF injection into striatum, the target area of dopaminergic neuron, may protect the dopaminergic neurons in the compact part of substantia nigra through retrograde transport. OBJECTIVE: To investigate the protective effect of intrastriatal GDNF on dopaminergic neurons in the substantia nigra of mice with Parkinson disease (PD), and analyze the action pathway. DESIGN: A controlled observation. SETTING: Neurobiological Laboratory of Xuzhou Medical College. MATERIALS: Twenty-four male Kunming mice of 7 - 8 weeks old were used. GDNF, 1-methy1-4-pheny1-1,2,3,6-tetrahydropyridine (MPTP) were purchased from Sigma Company (USA); LEICAQWin image processing and analytical system. METHODS: The experiments were carded out in the Neurobiological Laboratory of Xuzhou Medical College from September 2005 to October 2006. The PD models were established in adult KunMing mice by intraperitoneal injection of MPTP. The model mice were were randomly divided into four groups with 6 mice in each group: GDNF 4-day group, phosphate buffer solution (PSB) 4-day group, GDNF 6-day group and PSB 6-day group. Mice in the GDNF 4 and 6-day groups were administrated with 1 μ L GDNF solution (20 μ g/L, dispensed with 0.01 mol/L PBS) injected into right striatum at 4 and 6 days after model establishment. Mice in the PSB 4 and 6-day groups were administrated with 0.01 mol/L PBS of the same volume to the same injection at corresponding time points. ② On the 12^th day after model establishment, the midbrain tissue section of each mice was divided into 3 areas from rostral to caudal sides. The positive neurons of tyroxine hydroxylase (TH) and calcium binding protein (CB) with obvious nucleolus and clear outline were randomly selected for the measurement, and the number of positive neurons in unit area was counted. MAIN OUTCOME MEASURES: Number of positive neurons of TH and CB in midbrain substantia nigra of mice in each group. RESULTS: All the 24 mice were involved in the analysis of results. The numbers of TH^+ and CB^+ neurons in the GDNF 4-day group (54.33±6.92, 46.33±5.54) were obviously more than those in the PBS 4-day group (27.67±5.01, 21.50±5.96, P 〈 0.01). The numbers of TH^+ and CB^+ neurons in the GDNF 6-day group (75.67±5.39, 69.67±8.69) were obviously more than those in the PBS 6-day group (27.17±4.50, 21.33 ±5.72, P 〈 0.01) and those in the GDNF 4-day group (P 〈 0.01 ). CONCLUSION: Intrastriatal GDNF can protect dopaminergic neurons in substantia nigra of PD mice, and it may be related to the increase of CB expression. 展开更多
关键词 glial cell line-derived neurotrophic factor gdnf dopaminergic neurons 1 -methy1-4-pheny1- 1 2 3 6-tetrahydropyridine (MPTP)
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中枢疲劳恢复期大鼠海马GDNF、GFRα-1mRNA及其蛋白表达的动态变化特征 被引量:2
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作者 陈万 田诗彬 吴春燕 《山东体育学院学报》 北大核心 2015年第2期68-73,共6页
目的:探讨大鼠海马组织胶质细胞源性神经营养因子(glial cell line-derived neurotrophic factor,GDNF)、GDNF家族受体α-1信使RNA(GDNF?family receptorα-1mRNA,GFRα-1mRNA)及其蛋白表达在中枢疲劳后恢复期不同时相的动态变化特征。... 目的:探讨大鼠海马组织胶质细胞源性神经营养因子(glial cell line-derived neurotrophic factor,GDNF)、GDNF家族受体α-1信使RNA(GDNF?family receptorα-1mRNA,GFRα-1mRNA)及其蛋白表达在中枢疲劳后恢复期不同时相的动态变化特征。方法:雄性2月龄SD大鼠32只,随机分为对照组(C组,n=8)、实验组(E组,n=24);E组进行7周疲劳模型运动后,又随机分为运动后即刻组(E0组,n=8)、恢复期12 h组(E1组,n=8)、恢复期24 h组(E2组,n=8)。C组正常笼养,E组进行7周递增负荷跑台训练。经7周疲劳模型运动后即刻,C组和E0组腹腔注射10%水合氯醛糖浆(0.3m L/100g)麻醉后取海马组织,用于测定5-羟色胺(5-hydroxytryptamine,5-HT)、多巴胺(dopamine,DA)、GDNF、GFRα-1mRNA及其蛋白表达;E1组和E2组分别在恢复期12 h、24 h做上述同样取材和测试。结果:1)大鼠经7周递增负荷跑台训练后即刻,海马组织5-HT升高(P<0.01),DA下降(P<0.01),DA/5-HT下降(P<0.05)。2)运动后即刻海马组织GDNF、GFRα-1mRNA相对表达率和GDNF、GFRα-1平均蛋白表达水平升高;恢复期12 h高于C组和E0组(P<0.01);恢复期24 h降低并低于E1组(P<0.01)。结论:1)经7周疲劳模型运动后大鼠已经出现中枢疲劳。2)运动性中枢疲劳后大鼠海马组织GDNF、GFRα-1mRNA及其蛋白表达水平上升,提示GDNF和GFRα-1可能参与了中枢疲劳恢复的神经生物学调控过程。 展开更多
关键词 中枢疲劳 运动性疲劳 大鼠 海马组织 胶质细胞源性神经营养因子 胶质细胞源性神经营养因子受体
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GDNF及其受体GFRα1在小儿肾母细胞瘤中的表达及意义
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作者 张雪 田娟 +1 位作者 赵越超 郭芳 《天津医药》 CAS 2015年第6期628-630,I0001,共4页
目的研究胶质细胞源性神经营养因子(GDNF)及GDNF受体α1(GFRα1)在小儿肾母细胞瘤中的表达及其临床意义。方法应用免疫组织化学法检测GDNF及其受体GFRα1在30例小儿肾母细胞瘤组织及16例瘤旁正常肾组织病理石蜡标本中的表达。结果 GDNF... 目的研究胶质细胞源性神经营养因子(GDNF)及GDNF受体α1(GFRα1)在小儿肾母细胞瘤中的表达及其临床意义。方法应用免疫组织化学法检测GDNF及其受体GFRα1在30例小儿肾母细胞瘤组织及16例瘤旁正常肾组织病理石蜡标本中的表达。结果 GDNF在肾母细胞瘤中的阳性表达率高于瘤旁正常肾组织(66.7%vs6.3%),GFRα1在肾母细胞瘤中的阳性表达率高于瘤旁正常肾组织(63.3%vs 6.3%);两者在上皮型和胚芽成分强烈表达,在间叶成分表达较弱。GDNF及其受体GFRα1在不同组织分型、临床分期及有无淋巴结转移的患者间表达差异无统计学意义。结论肾母细胞瘤中GDNF及其受体GFRα1的高表达可能与肿瘤的发生密切相关。 展开更多
关键词 肾母细胞瘤 胶质细胞源性神经营养因子 gdnf受体α1 免疫组织化学
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