Chinese Journal of Tissue Engineering Research ›› 2011, Vol. 15 ›› Issue (33): 6139-6142.doi: 10.3969/j.issn.1673-8225.2011.33.015

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Effect of α-asarone on construction of intractable epilepsy cell models by culturing hippocampal neurons with magnesium-free extracellular solution

Wu Yue-juan, Wu Yuan, Su Jie, Tang Yu-lan, Yu Lu, Ma Mei-gang, Liu Yun   

  1. Department of Neurology, First Affiliated Hospital of Guangxi Medical University, Nanning  530021, Guangxi Zhuang Autonomous Region, China
  • Received:2011-01-14 Revised:2011-03-15 Online:2011-08-13 Published:2011-08-13
  • Contact: Wu Yuan, M.D., Professor, Department of Neurology, First Affiliated Hospital of Guangxi Medical University, Nanning 530021, Guangxi Zhuang Autonomous Region, China wuyuan90@126.com
  • About author:Wu Yue-juan★, Studying for master’s degree, Department of Neurology, First Affiliated Hospital of Guangxi Medical University, Nanning 530021, Guangxi Zhuang Autonomous Region, China 250791581@qq.com
  • Supported by:

    the National Natural Science Foundation of China, No. 30960111*; Medical Health Key Program of Guangxi Zhuang Autonomous Region, No. Guiweizhong200916*

Abstract:

BACKGROUND: The hippocampal neurons exposed to magnesium-free extracellular solution could develop and express spontaneous recurrent epileptionform discharges. The model can be used as intractable epilepsy cell models in the clinic.
OBJECTIVE: To investigate the protective effect of α-asarone on intractable spilepsy cell models.
METHODS: The rat hippocampal neurons were harvested within 24 hours after rat birth. The neurons were identified by immunochemistry and cultured with 7.5, 15, 30, 60, 120 mg/L α-asarone. After 4 hours, the hippocampal neurons were exposed to magnesium-free extracellular solution to establish intractable spilepsy cell models. After 3 hours, the neurons were cultured with medium containing α-asarone for 24 hours. The vitality of hippocampal neurons was detected by thiazolyl blue tetrazolium bromide.
RESULTS AND CONCLUSION: Following culture with magnesium-free extracellular solution, the vitality of hippocampal neurons was significantly decreased (P < 0.01), and after culture with α-asarone, the vitality of hippocampal neurons was relatively increased. These results demonstrated that α-asarone can alleviate the damage to neurons in intractable spilepsy, exhibiting a protective effect on neurons in a dose-dependent manner.

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