吉林大学学报(医学版)

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抗精神病药奎硫平对大鼠海马神经元死亡和细胞周期的影响

刘颖1,2, 张萱3, 刘纯岩4,倪文杰1,毛洪涛1,王珍琦1   

  1. (1.吉林大学公共卫生学院 卫生部放射生物学重点实验室,吉林 长春 130021;2.吉林省
    妇幼保健院中心实验室,吉林 长春130061;3.吉林大学第二医院科教科,吉林 长春130041;4.吉林大学第二医院放射线科,吉林 长春 130041 )
  • 收稿日期:2013-04-08 出版日期:2014-01-28 发布日期:2014-01-28
  • 通讯作者: 王珍琦 E-mail:(Tel:0431-85619443,E-mail:wangzq@jlu.edu.cn)
  • 作者简介:刘 颖(1973-),女,吉林省长春市人,副教授,医学硕士,主要从事抗精神病药神经保护作用的研究。
  • 基金资助:

    国家自然科学基金资助课题(30800363); 吉林大学基本科研业务费项目资助课题(2009);吉林大学“大学生创新创业训练计划”项目资助课题(2012)

Effect of quetiapine on death and cell cycle of rat hippocampus neurons

LIU Ying1,2,ZHANG Xuan3,LIU Chun-yan4,NI Wen-jie1,MAO Hong-tao1,WANG Zhen-qi1
   


  1.  (1.Key Laboratory of Radiobiology,Ministry of Health,School of Public Health,Jilin University,Changchun 130021,China;2. Central Laboratory,Jilin Women and Children Health Hospital,Changchun 130061,China;3. Department of Science and Education,Second Hospital,Jilin University,Changchun 130041,China;4. Department of Radiology,Second Hospital,Jilin University,Changchun 130041,China)
  • Received:2013-04-08 Online:2014-01-28 Published:2014-01-28

摘要:

目的:探讨抗精神病药奎硫平对谷氨酸损伤的海马神经元凋亡、坏死及细胞周期的影响,阐明其对神经系统的作用机制。方法:采用体外原代培养的大鼠海马神经元,复制谷氨酸损伤模型,实验分为正常对照组、谷氨酸损伤组和奎硫平(0.1、1.0、10.0、50.0、100.0、200.0和500.0   μmol•L-1)组,在体外通过流式细胞术(FCM)测定奎硫平应用前后神经元凋亡、坏死和细胞周期的改变。结果:谷氨酸损伤组较正常对照组细胞凋亡率增加 (P<0.01 );与谷氨酸损伤组比较,50.0~ 200.0   μmol•L-1奎硫平组细胞凋亡率降低(P<0.05,P<0.01)。谷氨酸损伤组坏死细胞较正常对照组升高2.9倍 (P<0.05 );与谷氨酸损伤组比较,0.1   μmol•L-1奎硫平组坏死细胞比例降低 (P<0.05 ),为谷氨酸损伤组的52.0%。与正常对照组比较,谷氨酸损伤组G0/G1期细胞百分数增加 (P<0.001),S期细胞百分数下降(P<0.01),G2+M期细胞百分数变化不明显。与谷氨酸损伤组比较,200.0   μmol•L-1奎硫平组G0/G1期细胞百分数降低 (P<0.05 ),为谷氨酸损伤组的68.9%;S期细胞百分数升高 (P<0.05 ),为谷氨酸损伤组的3.4倍。结论:奎硫平能够抵抗谷氨酸诱导的神经元损伤,减少细胞凋亡和坏死,改变细胞周期进程。

关键词: 奎硫平, 细胞周期, 细胞凋亡, 谷氨酸, 神经元, 神经保护作用

Abstract:

To investigate the effects of antidepressant quetiapine on the apoptosis,necrosis and cell cycle of the hippocampus neurons injured by glutamate (Glu),and to demonstrate the mechanism of quetiapine on nervous system.Methods Primary cultured hippocampal neurons were injured with Glu.Normal control group,Glu injury group and quetiapine (0.1,1.0,10.0,50.0,100.0,200.0, and 500.0  μmol•L-1 ) group were set up. The changes in apoptosis,necrosis and cell cycle of neurons were detected by FCM before and after administration with quetiapine.Results Compared with normal control group,the percentage of apoptotic neurons in Glu injury group was increasd (P<0.01);compared with Glu injury group,the apoptotic rates in 50.0-200.0  μmol•L-1 quetiapine groups were decreased (P<0.05,P<0.01).The necrotic  rate in Glu injury group was increased to 2.9 times compared with normal control group (P<0.05 );compared with Glu injury group,the necrotic  rate of neurons in 0.1   μmol•L-1 quetiapine group was decreased (P<0.05).Compored with normal control group,the percentage of neurons in G0/G1 phase in Glu injury group was increased (P<0.001),the percentage of of neurons in S phase was decreased (P<0.01),and the  percentage of neurons in G2+M phase didn’t change significantly. Compared with Glu injury group,the percentage of neurons in G0/G1 phase in 200.0   μmol•L-1 quetiapine group was decresed,which was  decreased to 68.9% of that in Glu injury group,and the percentage of neurons in S phase was increased to 3.4 times of that in Glu injury group (P<0.05).Conclusion Quetiapine can prevent the hippocampal neurons from the damage induced with Glu,decrease the apoptosis and necrosis,and change the cell cycle.

Key words: quetiapine, cell cycle, apoptosis, glutamate, neuron, neuroprotection

中图分类号: 

  • R965