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[全脑缺血成年大鼠中增殖性神经祖细胞的周期性数量变化]

[Periodic quantity variation of proliferating neuronal progenitors in adult rats after global brain ischemia].

作者信息

Li Ou, Zhu Xin-hong, Gao Tian-ming

机构信息

Department of Neurobiology, Southern Medical University, Guangzhou 510515, China.

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2006 May;26(5):564-6, 569.

Abstract

OBJECTIVE

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.

METHODS

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.

RESULTS

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.

CONCLUSION

Increased proliferation of the neuroprogenitors occurs mainly within the initial 10 days after global ischemia in rats.

摘要

目的

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。

方法

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。

结果

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。

结论

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。

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