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围产期窒息后大鼠脑内NADPH-黄递酶反应性的短期变化。低温治疗的神经保护作用。

Short-term changes in NADPH-diaphorase reactivity in rat brain following perinatal asphyxia. Neuroprotective effects of cold treatment.

作者信息

Loidl C F, Capani F, López-Costa J J, Selvín-Testa A, López E M, Goldstein J, Pecci-Saavedra J

机构信息

Instituto de Biología Celular y Neurociencias, Prof. E. De Robertis, Facultad de Medicina, Universidad de Buenos Aires, Argentina.

出版信息

Mol Chem Neuropathol. 1997 Aug;31(3):301-16. doi: 10.1007/BF02815132.

DOI:10.1007/BF02815132
PMID:9336771
Abstract

Perinatal asphyxia (PA) produces changes in nitric oxide synthase (NOS) activity in neuronal and endothelial cells of the striatum and neocortex. The changes were examined using a histochemical NADPH-diaphorase (NADPH-d) staining method. Newborn rats were exposed to severe PA at 37 degrees C and other groups were subjected to severe PA under hypothermic condition (15 degrees C) for 20 or 100 min, respectively. Quantitative image analysis was performed on the striatum and neocortex in order to count cell number of reactive neurons and to compare the pattern of staining between the different groups of animals. Severe asphyctic pups showed an important neuronal loss in striatum and neocortex that was reduced by hypothermia. NADPH-d(+) neurons with reactive processes were found in the lateral zone of the striatum and neocortex in asphyctic pups. Controls and hypothermic striatum showed rounded cells without reactive process, while no cells were stained in cortex. There was also an increase in NADPH-d activity in endothelial cells in severe asphyctic pups in striatum and neocortex vs control and hypothermically treated animals. Our data evidenced that an inappropriate activation of NOS in neuronal and endothelial cells induced by PA is related to neuronal injury. Hypothermia inhibits neuronal injury and may be a valuable neuroprotective agent.

摘要

围产期窒息(PA)会使纹状体和新皮质的神经元及内皮细胞中的一氧化氮合酶(NOS)活性发生变化。采用组织化学烟酰胺腺嘌呤二核苷酸磷酸黄递酶(NADPH-d)染色法对这些变化进行检测。新生大鼠在37℃下暴露于严重PA,其他组分别在低温条件(15℃)下暴露于严重PA 20或100分钟。对纹状体和新皮质进行定量图像分析,以计算反应性神经元的细胞数量,并比较不同组动物之间的染色模式。严重窒息的幼崽在纹状体和新皮质中出现明显的神经元丢失,而低温可减轻这种丢失。在窒息幼崽的纹状体外侧区和新皮质中发现了具有反应性突起的NADPH-d(+)神经元。对照组和低温处理的纹状体显示出无反应性突起的圆形细胞,而皮质中无细胞被染色。与对照组和低温处理的动物相比,严重窒息幼崽的纹状体和新皮质中的内皮细胞中NADPH-d活性也有所增加。我们的数据表明,PA诱导的神经元和内皮细胞中NOS的不适当激活与神经元损伤有关。低温可抑制神经元损伤,可能是一种有价值的神经保护剂。

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Short-term changes in NADPH-diaphorase reactivity in rat brain following perinatal asphyxia. Neuroprotective effects of cold treatment.围产期窒息后大鼠脑内NADPH-黄递酶反应性的短期变化。低温治疗的神经保护作用。
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Front Pharmacol. 2021 Apr 8;12:651599. doi: 10.3389/fphar.2021.651599. eCollection 2021.
2
Perinatal asphyxia: current status and approaches towards neuroprotective strategies, with focus on sentinel proteins.围产期窒息:现状及神经保护策略的方法,重点关注哨兵蛋白。
Neurotox Res. 2011 May;19(4):603-27. doi: 10.1007/s12640-010-9208-9. Epub 2010 Jul 20.
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Plasticity of basal ganglia neurocircuitries following perinatal asphyxia: effect of nicotinamide.
围产期窒息后基底神经节神经回路的可塑性:烟酰胺的作用
Exp Brain Res. 2007 Jun;180(1):139-52. doi: 10.1007/s00221-006-0842-7. Epub 2007 Feb 20.