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成年大鼠短暂性前脑缺血后齿状回神经发生增强的区域差异。

Regional differences in enhanced neurogenesis in the dentate gyrus of adult rats after transient forebrain ischemia.

作者信息

Choi Yun-Sik, Lee Mun-Yong, Sung Ki-Wug, Jeong Seong-Whan, Choi Jeong-Sun, Park Hyun-Jung, Kim Ok Nyu, Lee Sang Bok, Kim Seong Yun

机构信息

Department of Pharmacology, The Catholic University of Korea, Seoul 137-701, Korea.

出版信息

Mol Cells. 2003 Oct 31;16(2):232-8.

Abstract

Neurogenesis in the dentate gyrus occurs throughout life. We observed regional differences in neurogenesis in the dentate gyrus of adult rats following transient forebrain ischemia. Nine days after ischemic-reperfusion or sham manipulation, rats were given 5-bromo-2'-deoxyuridine-5'-monophosphate (BrdU), a marker for dividing cells. They were killed 1 or 28 days later to distinguish between cell proliferation and survival. Neurogenesis was evaluated by BrdU incorporation as well by identifying neuronal and glial markers in six regions of the dentate gyrus: rostral, middle and caudal along the rostrocaudal axis, each further divided into suprapyramidal and infrapyramidal blade subregions. In control rats BrdU-positive cells in the rostral subregions were significantly lower in the suprapyramidal than in the infrapyramidal blades at both 1 and 28 days after BrdU injection. One day after injection, BrdU-positive cells had increased more in five of the subregions in the ischemic rats than in the controls, the exception being the suprapyramidal blade of the rostral subregion. At 28 days after BrdU injection, numbers of BrdU-positive cells were higher in four subregions in the ischemic group, the exceptions being the rostral suprapyramidal and middle infrapyramidal blades. At 28 days after BrdU injection, the percentages of BrdU positive cells that expressed a neuronal marker (NeuN) were the same in the dentate granule cell layers of ischemic and control rats. Our data thus demonstrate regional differences in enhanced neurogenesis in the dentate gyrus of adult rats after transient forebrain ischemia.

摘要

齿状回中的神经发生在整个生命过程中都存在。我们观察了成年大鼠短暂性前脑缺血后齿状回神经发生的区域差异。在缺血再灌注或假手术操作9天后,给大鼠注射5-溴-2'-脱氧尿苷-5'-单磷酸(BrdU),这是一种用于标记分裂细胞的物质。1天或28天后将它们处死,以区分细胞增殖和存活情况。通过BrdU掺入以及在齿状回的六个区域中鉴定神经元和神经胶质细胞标志物来评估神经发生:沿前后轴的前部、中部和后部,每个区域又进一步分为锥体上叶片和锥体下叶片亚区域。在对照大鼠中,在注射BrdU后1天和28天,前部亚区域锥体上叶片中的BrdU阳性细胞明显低于锥体下叶片。注射后1天,缺血大鼠的五个亚区域中BrdU阳性细胞的增加比对照大鼠更多,前部亚区域的锥体上叶片除外。在注射BrdU后28天,缺血组的四个亚区域中BrdU阳性细胞数量更高,前部锥体上叶片和中部锥体下叶片除外。在注射BrdU后28天,缺血大鼠和对照大鼠的齿状颗粒细胞层中表达神经元标志物(NeuN)的BrdU阳性细胞百分比相同。因此,我们的数据表明成年大鼠短暂性前脑缺血后齿状回中神经发生增强存在区域差异。

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