李玮, 石晋丽, 李琴, 段惠惠, 唐民科. 甘松新酮对缺糖缺氧损伤原代培养神经元的保护作用J. 药学学报, 2013,48(9): 1422-1429.
引用本文: 李玮, 石晋丽, 李琴, 段惠惠, 唐民科. 甘松新酮对缺糖缺氧损伤原代培养神经元的保护作用J. 药学学报, 2013,48(9): 1422-1429.
LI Wei, SHI Jin-li, LI Qin, DUAN Hui-hui, TANG Min-ke. Nardosinone reduces neuronal injury induced by oxygen-glucose deprivation in primary cortical cultures J. Acta Pharmaceutica Sinica, 2013,48(9): 1422-1429.
Citation: LI Wei, SHI Jin-li, LI Qin, DUAN Hui-hui, TANG Min-ke. Nardosinone reduces neuronal injury induced by oxygen-glucose deprivation in primary cortical cultures J. Acta Pharmaceutica Sinica, 2013,48(9): 1422-1429.

甘松新酮对缺糖缺氧损伤原代培养神经元的保护作用

Nardosinone reduces neuronal injury induced by oxygen-glucose deprivation in primary cortical cultures

  • 摘要: 观察甘松新酮对缺糖缺氧损伤原代培养神经元的保护作用。采用孕14天小鼠胚胎皮层制备原代培 养神经元; MTT法确定甘松新酮对原代培养神经细胞的安全剂量, 并观察其对缺糖缺氧神经元的保护作用; 采用Western blotting法观察药物对缺糖缺氧损伤神经元以及正常培养神经元蛋白激酶A (PKA) 和细胞外信号调节激酶 (ERK) 通路关键蛋白表达的影响。结果显示, 甘松新酮 (50和100 μmol·L-1) 能够增加缺糖缺氧损伤神经元的存活率 (P<0.01, 与OGD组比较); 同时, 能增加缺糖缺氧神经元PKA、小分子G蛋白Ras的相关蛋白1 (Rap1)、丝裂原激活的蛋白激酶的激酶1 (MEK1) 及磷酸化的ERK1/2 (p-ERK1/2) 的表达, 且此作用呈剂量依赖趋势。对正常培养神经元研究结果显示, 甘松新酮 (50、100和200 μmol·L-1) 也能增加其PKA、Rap1、MEK1及p-ERK1/2的表达 (P<0.01)。以上结果表明, 甘松新酮对缺糖缺氧损伤的原代培养神经元有明确保护作用, 该作用可能与药物激活PKA和ERK通路有关。

     

    Abstract: The aim of the study is to investigate the effect of nardosinone (Nar) on neuronal injury induced by oxygen-glucose deprivation (OGD) in primary cortical cultures isolated from embryos at gestational day 14. MTT method was used to determine the dosage regimen of Nar in primary neuronal cultures and observe the influence of Nar on the neurons suffering OGD; Western blotting analysis was used to detect expressions of protein kinase A (PKA), Ras related protein 1 (Rap1), mitogen-activated protein kinase kinase 1 (MEK1) and phospho-extracellular signal-regulated kinase 1/2 (p-ERK1/2) of OGD-injured or uninjured primary cultured neurons after Nar treatment. Results showed that Nar (50 and 100 μmol·L-1) improved the cell viability during OGD damage (P<0.01) and increased the expression of PKA, Rap1, MEK1 and p-ERK1/2 in injured neurons. Additionally, elevations of PKA, Rap1, MEK1 and p-ERK1/2 in uninjured neurons were caused by Nar (50, 100 and 200 μmol·L-1) with a dose-dependent tenclency as well (P<0.01). In conclusion, Nar could protect against the neuronal injury exposed to OGD, which may be relevant to the promotion of PKA and ERK signaling pathway.

     

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