Zhao Hong-Gang, Li Wen-Bin, Li Qing-Jun, Chen Xiao-Ling, Liu Hui-Qing, Feng Rong-Fang, Ai Jie
Department of Pathophysiology, Institute of Basic Medicine, Hebei Medical University, Shijiazhuang 050017, China.
Sheng Li Xue Bao. 2004 Jun 25;56(3):407-12.
The purpose of this study was to investigate the effects of limb ischemic preconditioning (LIP) on apoptosis of pyramidal neurons in the CA1 hippocampus induced by global cerebral ischemia-reperfusion in rats. Forty-six rats whose bilateral vertebral arteries were occluded permanently were assigned to one of four groups: sham group, limb ischemia group, cerebral ischemia group and LIP group. LIP was performed by occluding the bilateral femoral arteries for 10 min 3 times in an interval of 10 min. Global cerebral ischemia was underwent by occluding the bilateral common carotid arteries for 8 min immediately after LIP. Assays for apoptosis of the hippocampal neurons were biologically and morphologically performed using gel electrophoresis, TUNEL and AO/EB staining. Characteristic DNA ladder was clearly visualized with gel electrophoresis in the hippocampus in cerebral ischemia group, but not in LIP group. The number of TUNEL-positive cells in the CA1 hippocampus was significantly reduced by LIP from 69.8+/-12 (cerebral ischemia group) to 17.8+/-5.8 (P<0.01). AO/EB staining also showed a reduction of apoptosis in LIP group compared with cerebral ischemia group. These results suggest that LIP can inhibit hippocampal neuronal apoptosis induced by cerebral ischemia-reperfusion, which contributes to the protection against the delayed neuronal death induced by cerebral ischemic insult.
本研究旨在探讨肢体缺血预处理(LIP)对大鼠全脑缺血再灌注诱导的海马CA1区锥体神经元凋亡的影响。将46只双侧椎动脉永久闭塞的大鼠分为四组之一:假手术组、肢体缺血组、脑缺血组和LIP组。通过双侧股动脉闭塞10分钟,间隔10分钟,重复3次来进行LIP。在LIP后立即通过双侧颈总动脉闭塞8分钟进行全脑缺血。使用凝胶电泳、TUNEL和AO/EB染色从生物学和形态学上对海马神经元凋亡进行检测。在脑缺血组海马中通过凝胶电泳可清晰观察到特征性DNA梯带,但在LIP组中未观察到。LIP使海马CA1区TUNEL阳性细胞数量从脑缺血组的69.8±12显著减少至17.8±5.8(P<0.01)。AO/EB染色也显示LIP组与脑缺血组相比凋亡减少。这些结果表明,LIP可抑制脑缺血再灌注诱导的海马神经元凋亡,这有助于保护免受脑缺血损伤诱导的迟发性神经元死亡。