• Both simvastatin and CDPC can relieve the damages of the brain in rats HIBD.

    辛伐他汀和胞二磷胆碱可减轻新生大鼠hibd后脑组织损害。

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  • Objective To observe the electric physiologic changes in newborn piglets with HIBD.

    目的观察缺氧缺血性脑损伤新生猪脑电生理的变化。

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  • RESULTS: In the behavioral tests, HIBD rats performed significantly worse than control rats.

    结果:在行为测试中,HIBD组大鼠的成绩显著低于正常鼠。

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  • Objective To develop an improved neonatal piglet model of hypoxic ischemic brain damage (HIBD).

    目的研究新生猪缺氧缺血脑损伤(HIBD)模型的制备。

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  • Knock-down of endogenous protective process of MLT maybe plays a part in early HIBD pathogenic mechanism.

    降低了MLT的内源性保护作用可能参与早期HIBD的发病机制。

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  • Objective To evaluate treatment response of scopolamine for hypoxic-ischaemic brain damage(HIBD) in neonates.

    目的探索东莨菪碱对新生儿缺氧缺血性脑损伤(HIBD)的治疗作用。

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  • The hypoxic ischemic brain damage (HIBD) seen in survivors with prenatal or postnatal asphyxia is a major cause of disabilities.

    新生儿缺氧缺血性脑损伤是人类致残的主要原因之一。

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  • Objective To study the expression of ICAM 1 at gene transcription level in neonatal rats after hypoxic ischemic brain damage(HIBD).

    目的研究新生动物缺氧缺血性脑损伤(HIBD)后脑细胞间粘附分子-1(ICAM- 1)在转录水平表达规律。

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  • AIM To study the protective effects of monosialotetrahexosylganglioside (GM1) after hypoxic ischemic brain damage (HIBD) in neonatal rats.

    目的研究外源性单唾液酸四己糖神经节苷脂(GM1)对新生鼠缺氧缺血脑损伤(HIBD)的保护作用。

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  • Hypoxia ischemic brain damage (HIBD), which resulted from neonatal asphyxia, is the main cause of death and disability in neonatal periods.

    围产期窒息所致缺氧缺血性脑损伤(HIBD)是新生儿死亡和残疾的主要原因。

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  • Aim: To study the effects of epicranium medication injection treatment on learning and memory in brain cells of hypoxic-ischemic brain damage (HIBD).

    目的:探讨头部药物位点注射对缺氧缺血性脑损伤(HIBD)后学习和记忆的影响。

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  • The GFAP increases in damaged cerebral cortex in the recovery stage of neonatal rat HIBD, suggesting that GFAP participates the repair of lesion region.

    新生鼠hibd恢复期,脑损伤部位的GFAP明显增加,提示其可能参与了损伤区的修复。

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  • Objective To observe the variations in the expression levels of interleukin-16(IL-16) protein in neonatal rats with hypoxic-ischemic brain damage(HIBD).

    目的观察缺氧缺血性脑损伤(HIBD)新生大鼠白细胞介素-16(IL-16)表达的变化。

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  • To explore the pathologic and DNA changes in the brain of the hypoxic ischemic brain damage (HIBD) newborn rats after exposed to high oxygen for long time.

    观察缺氧缺血性脑损伤(HIBD)新生大鼠长时间吸高浓度氧后脑病理学及DNA损伤的变化。

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  • In this review, we summarized relationship between apoptosis and neonatal hypoxic-ischemic brain damage (HIBD) and importance of apoptosis mechanism in HIBD.

    该文主要阐述细胞凋亡与新生儿缺氧缺血性脑损伤的关系,提出细胞凋亡机制在缺氧缺血性脑损伤中的重要性。

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  • Objective To study the repairing effects of epicranium medication injection treatment on brain cells of hypoxic-ischemic brain damage (HIBD) and its mechanism.

    目的研究头皮药物位点注射对缺氧缺血性脑损伤(HIBD)后脑细胞的修复作用。

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  • Objective to study the repairing effects of nerve cells on HIBD with Epicranium Medication Injection treatment on site, and to explore the mechanism of action.

    目的:研究头皮药物位点注射疗法对缺氧缺血性脑损伤(HIBD)后,神经细胞修复作用的疗效及探讨其作用机理。

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  • Objective to explore the influences of early interventions on learning, memory and neuron apoptosis in the brain of neonatal rats with hypoxic ischemic brain damage (HIBD).

    目的探讨早期干预对缺氧缺血性脑损伤(HIBD)大鼠学习记忆能力及神经元凋亡的影响。

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  • Conclusion The role of environmental stimulation in functional outcome of HIBD is likely to be related to change of synaptic substructure and increased synaptic plasticity.

    结论环境刺激对HIBD大鼠功能的促进作用可能与突触超微结构参数的改变,增强突触可塑性有关。

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  • Objective: To study the effect of the neonatal handling and enriched environmental stimulation on brain function of rats with hypoxic-ischemic brain damage (HIBD) in uterus.

    目的:探讨早期触摸和环境刺激对宫内缺血缺氧性脑损伤(HIBD)大鼠脑功能的影响。

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  • Objective To study the role of endogenous carbon monoxide(CO) in newborn rats with hypoxic-ischemic brain damage (HIBD) and the protective effect of Sn-protoporphyrin (SnPP).

    目的探讨内源性一氧化碳(CO)在新生大鼠缺氧缺血性脑损伤(HIBD)中的作用机制及锡原卟啉的保护作用。

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  • Objective: To study the changes of pathology, ATP production rate and ATP synthase activity in hippocampal cortex of neonatal pigs after hypoxic-ischemic brain damage (HIBD).

    目的:研究缺氧缺血性脑损害新生猪海马皮层病理改变及ATP生成率、ATP合成酶活性变化。

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  • Objective To investigate the changes of blood coagulation state and some prothrombin's function in newborn piglets at different time after hypoxic-ischemic brain damage (HIBD).

    目的研究缺氧缺血新生猪凝血状态,以及部分凝血因子促凝活性的动态变化,探讨缺氧缺血性脑损伤(HIBD)时凝血功能变化。

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  • Objective To study the neuroprotective effects of lamotrigine (LTG) on hypoxic-ischemic brain damage (HIBD) in neonatal rats, and the influence of administration time and dosage.

    目的研究拉莫三嗪(ltg)对缺氧缺血性脑损伤(HIBD)新生大鼠的神经保护作用,以及不同用药剂量和用药时间对该作用的影响。

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  • Conclusions Pretreatment with baicalin, as with Dex, has a protective effect against HIBD in neonatal rats, but baicalin or Dex post-treatment do not reverse the neuronal injuries.

    结论黄芩苷及地塞米松预处理对新生大鼠hibd产生保护作用,能减少神经元凋亡,而后处理无效。

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  • Objective To observe the change of neuron-specific enolase (NSE) and glial fibrillary acidic protein (GFAP) in neonatal rats' cerebral cortex with hypoxic-ischemic brain damage (HIBD).

    目的了解新生鼠缺氧缺血性脑损伤(HIBD)时大脑皮质神经元特异性烯醇化酶(nse)和胶质纤维酸性蛋白(GFAP)的变化。

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  • Through investigating the effect of mild hypothermia on activity of nitric oxide synthase(NOS) in cortical neurons and glycemia levels of neonatal rats with hypoxic ischemic brain damage(HIBD).

    通过亚低温对新生鼠缺氧缺血性脑损伤(HIBD)大脑皮质神经元一氧化氮合酶(NOS)及血糖水平影响的研究,探讨亚低温对缺氧缺血性脑损伤的保护作用机制。

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  • Objective to observe the expression of proliferation in hippocampus following hypoxic-ischemic brain damage (HIBD) in neonatal rats and to explore the possible endogenous neurogenesis of brain.

    目的:观察新生大鼠缺氧缺血性脑损伤(HIBD)后海马区细胞增殖的情况,探讨脑组织内源性修复的可能机制。

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  • Objective to study the morphologic changes of mitochondria and metabolic protective effect of fructose 1 6 diphosphate (FDP) intervention in newborn rats with hypoxic ischemic brain damage (HIBD).

    目的探讨16二磷酸果糖(FDP)干预治疗新生鼠缺氧缺血性脑损伤(HIBD)后脑神经细胞线粒体形态学变化及对能量代谢的影响。

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  • Objective To explore the effect of N-acetylcysteine (NAC) on intercellular adhesion molecule-1(ICAM-1) expression and apoptosis in neonatal rats brain after hypoxic and ischemic brain damage (HIBD).

    目的探讨N-乙酰半胱氨酸(NAC)对缺氧缺血脑损伤(HIBD)大鼠脑细胞间黏附分子-1及细胞凋亡的影响。

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