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睫状神经营养因子对大鼠海马缺血性细胞损伤的影响。

Effect of CNTF on ischaemic cell damage in rat hippocampus.

作者信息

Ogata N, Ogata K, Imhof H G, Yonekawa Y

机构信息

Department of Neurosurgery, University Hospital of Zurich, Switzerland.

出版信息

Acta Neurochir (Wien). 1996;138(5):580-3. doi: 10.1007/BF01411179.

Abstract

The neuroprotective effect of neurotrophic factors has been demonstrated in experimental cerebral ischaemia recently. These include nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), insulin-like growth factor-1 (IGF-1), and basic fibroblast growth factor (basic FGF). The neuroprotective effect of ciliary neurotrophic factor (CNTF), however, has not been studied so far. We have examined the neuroprotective effect of recombinant rat CNTF in a rat forebrain ischaemia model. A continuous infusion of CNTF was started 1 week before the induction of ischaemia and continued until 1 week after the ischaemia. Reversible forebrain ischaemia was induced by 7 minutes of bilateral carotid occlusion with hypotension. Neuronal cell death in the hippocampal CA1 sector was evaluated 1 week after the ischaemia. For the control group artificial CSF (cerebrospinal fluid) was infused instead of CNTF. Per cent neuronal cell death was 83.4 +/- 5.9% (mean +/- SEM, n = 5) in the control group, and 71.1 +/- 10.0% (mean +/- SEM, n = 5) in the CNTF group. Although percentage of neuronal cell death was lower in the CNTF group, the difference was not statistically significant. This result suggests that the protective effect of CNTF in the rat forebrain ischaemia model may be limited compared with other neurotrophic factors. It is considered that the number of neurons protected by CNTF may be small.

摘要

神经营养因子的神经保护作用最近已在实验性脑缺血中得到证实。这些因子包括神经生长因子(NGF)、脑源性神经营养因子(BDNF)、胰岛素样生长因子-1(IGF-1)和碱性成纤维细胞生长因子(碱性FGF)。然而,睫状神经营养因子(CNTF)的神经保护作用迄今尚未得到研究。我们在大鼠前脑缺血模型中研究了重组大鼠CNTF的神经保护作用。在缺血诱导前1周开始持续输注CNTF,并持续至缺血后1周。通过双侧颈动脉闭塞伴低血压7分钟诱导可逆性前脑缺血。在缺血后1周评估海马CA1区的神经元细胞死亡情况。对照组输注人工脑脊液(CSF)而非CNTF。对照组神经元细胞死亡百分比为83.4±5.9%(平均值±标准误,n = 5),CNTF组为71.1±10.0%(平均值±标准误,n = 5)。虽然CNTF组神经元细胞死亡百分比较低,但差异无统计学意义。该结果表明,与其他神经营养因子相比,CNTF在大鼠前脑缺血模型中的保护作用可能有限。据认为,受CNTF保护的神经元数量可能较少。

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