Neural Regeneration Research ›› 2013, Vol. 8 ›› Issue (10): 916-921.doi: 10.3969/j.issn.1673-5374.2013.10.006

Previous Articles     Next Articles

Transcription factor changes following long term cerebral ischemia/reperfusion injury

Hongbo Zhang1, Weijuan Gao2, Tao Qian3, Jinglong Tang1, Jun Li1   

  1. 1 Department of Pathophysiology, Chengde Medical College, Chengde 067000, Hebei Province, China
    2 Hebei Chemical and Pharmaceutical College, Shijiazhuang 050026, Hebei Province, China
    3 Hebei Provincial People's Hospital, Shijiazhuang 050051, Hebei Province, China
  • Received:2012-09-15 Revised:2013-01-04 Online:2013-04-05 Published:2013-04-05
  • Contact: Weijuan Gao, M.D, Ph.D., Professor, Hebei Chemical and Pharmaceutical College, Shijiazhuang 050026, Hebei Province, China, gwj6088@ 163.com.
  • About author:Hongbo Zhang★, Master, Lecturer.

Abstract:

The present study established a rat model of cerebral ischemia/reperfusion injury using four-vessel occlusion and found that hippocampal CA1 neuronal morphology was damaged, and that there were reductions in hippocampal neuron number and DNA-binding activity of cAMP response element binding protein and CCAAT/enhancer binding protein, accompanied by decreased learning and memory ability. These findings indicate that decline of hippocampal cAMP response element binding protein and CCAAT/enhancer binding protein DNA-binding activities may contribute to neuronal injury and learning and memory ability reduction induced by cerebral ischemia/reperfusion injury.

Key words: neural regeneration, brain injury, cerebral ischemia/reperfusion, hippocampus, cAMP response element binding protein, CCAAT/enhancer binding protein, DNA-binding activity, brain, grants-supported paper, neuroregeneration