| 重复性低氧增高小鼠脑组织内CREB的磷酸化水平 |
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| 引用本文： | 高亚南,高歌,龙彩瑕,牛晨晨,徐群渊,李俊发. 重复性低氧增高小鼠脑组织内CREB的磷酸化水平[J]. 神经解剖学杂志, 2006, 22(2): 183-186 |
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| 作者姓名： | 高亚南 高歌 龙彩瑕 牛晨晨 徐群渊 李俊发 |
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| 作者单位： | 首都医科大学,神经生物学系,疼痛生物医学研究所,北京神经再生修复重点实验室,北京,100054;首都医科大学,神经生物学系,疼痛生物医学研究所,北京神经再生修复重点实验室,北京,100054;首都医科大学,神经生物学系,疼痛生物医学研究所,北京神经再生修复重点实验室,北京,100054;首都医科大学,神经生物学系,疼痛生物医学研究所,北京神经再生修复重点实验室,北京,100054;首都医科大学,神经生物学系,疼痛生物医学研究所,北京神经再生修复重点实验室,北京,100054;首都医科大学,神经生物学系,疼痛生物医学研究所,北京神经再生修复重点实验室,北京,100054 |
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| 基金项目： | 中国科学院资助项目;北京市自然科学基金;教育部优秀青年教师资助计划;北京市教委科技发展计划项目 |
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| 摘 要： | 为探讨cAMP反应元件结合蛋白(CREB)在小鼠脑低氧预适应形成过程中的作用,本研究应用Westernblot技术结合GelDoc凝胶成像系统,半定量检测了整体低氧预适应模型小鼠脑组织内CREB的磷酸化水平和非磷酸化水平的表达水平。结果显示:(1)随低氧暴露次数(H1H4)的增加,小鼠海马组织内CREB的磷酸化水平(激活程度)明显增高(P<0.05;n=7);同样,大脑皮层内CREB的磷酸化水平也随低氧暴露次数(H1H4)的增加而明显增高(P<0.05,n=7);(2)随低氧暴露次数(H1H4)的增加,CREB的蛋白表达量无论在小鼠海马组织还是皮层组织内均无明显变化。以上结果提示CREB磷酸化水平的增高(激活)可能参与了脑低氧预适应的形成过程。
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| 关 键 词： | 脑低氧预适应 CREB 磷酸化 海马 大脑皮层 |
| 收稿时间： | 2005-07-04 |
| 修稿时间： | 2005-07-04 |
THE LEVEL OF CREB PHOSPHORYLATION IN THE BRAIN OF MICE IS INCREASED BY REPETITIVE HYPOXIA |
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| Gao Yanan,Gao ge,Long Caixia,Niu Chenchen,Xu Qunyuan,Li Junfa. THE LEVEL OF CREB PHOSPHORYLATION IN THE BRAIN OF MICE IS INCREASED BY REPETITIVE HYPOXIA[J]. Chinese Journal of Neuroanatomy, 2006, 22(2): 183-186 |
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| Authors: | Gao Yanan Gao ge Long Caixia Niu Chenchen Xu Qunyuan Li Junfa |
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| Affiliation: | Institute for Biomedical Sciences of Pain, and Beijing Key Laboratory for Neural Regeneration and Repairing, Department of Neurobiology, Capital University of Medical Sciences, Beijing 100054 |
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| Abstract: | To explore the role of cAMP response element binding protein(CREB) in the development of cerebral hypoxic preconditioning. Western blot and Gel Doc imaging system were applied to semi-quantitatively analyze the effect of repetitive hypoxic exposure (H1-H4) on the levels of CREB phosphorylation and protein expression in the brain of mice. The results showed that: (1) The levels of CREB phosphorylation were enhanced in response to the repetitive hypoxic exposure (H1-H4) both in the hippocampus and the cortex of mice. The statistic significance could be found at H1-H4 groups for both the hippocampus and the cortex (P<0.05, n=7); (2) No any significant changes could be found in the level of CREB protein expression both in the hippocampus and the cortex of mice. The preseat results suggest that the activation of CREB might be involved in the development of cerebral hypoxic preconditioning. |
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| Keywords: | cerebral hypoxic preconditioning CREB phosphorylation hippocampus cortex |
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