Li Ou, Zhu Xin-hong, Gao Tian-ming
Department of Neurobiology, Southern Medical University, Guangzhou 510515, China.
Nan Fang Yi Ke Da Xue Xue Bao. 2006 May;26(5):564-6, 569.
To investigate the periodic quantity variation of proliferating neuronal progenitors after global brain ischemia and provide evidence for choosing the time-window of drug therapy to promote neuronal regeneration after ischemia.
Adult male Wistar rats were subjected to 15-min global brain ischemia (four-vessel occlusion model) and randomized subsequently into 8 groups (n=3). The rats were given intraperitoneal injections of BrdU (75 mg/kg) for 4 times daily (at a 2-hour interval) since day 7 till day 11 after ischemia, and on day 29, the rats were perfused transcardially for fixation. Another 3 normal rats were given BrdU in the same manner and killed the next day. Coronal sections of the brain tissue (30 microm) were prepared for immunocytochemical detection of BrdU-labeled cells and immunofluorescent detection of BrdU/NeuN double-labeled cells. The density of BrdU-positive cells and BrdU/NeuN double-labeled cells in the hippocampal dentate gyrus (DG) and CA1 region were counted and the density of proliferating cells at different days after ischemia were compared using one-way ANOVA.
The proliferation of the neuronal progenitors increased after global brain ischemia. The number of BrdU-positive cells in the DG and CA1 region decreased gradually in 7-10 days after ischemia, and reached the normal level during 11-14 days. The differentiation of the progenitors did not vary after ischemia.
Increased proliferation of the neuroprogenitors occurs mainly within the initial 10 days after global ischemia in rats.
探讨全脑缺血后增殖性神经祖细胞的周期性数量变化,为选择促进缺血后神经元再生的药物治疗时间窗提供依据。
成年雄性Wistar大鼠接受15分钟全脑缺血(四血管闭塞模型),随后随机分为8组(n = 3)。自缺血后第7天至第11天,每天给大鼠腹腔注射BrdU(75 mg/kg)4次(间隔2小时),在第29天,经心脏灌注固定大鼠。另外3只正常大鼠以同样方式给予BrdU并于次日处死。制备脑组织冠状切片(30微米)用于免疫细胞化学检测BrdU标记细胞以及免疫荧光检测BrdU/NeuN双标记细胞。计数海马齿状回(DG)和CA1区BrdU阳性细胞及BrdU/NeuN双标记细胞的密度,并采用单因素方差分析比较缺血后不同天数增殖细胞的密度。
全脑缺血后神经祖细胞的增殖增加。DG和CA1区BrdU阳性细胞数量在缺血后7 - 10天逐渐减少,并在11 - 14天达到正常水平。缺血后祖细胞的分化没有变化。
大鼠全脑缺血后神经祖细胞增殖增加主要发生在最初10天内。