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本文引用的文献

1
Brain barrier properties and cerebral blood flow in neonatal mice exposed to cerebral hypoxia-ischemia.暴露于脑缺氧缺血的新生小鼠的脑屏障特性和脑血流量
J Cereb Blood Flow Metab. 2015 May;35(5):818-27. doi: 10.1038/jcbfm.2014.255. Epub 2015 Jan 28.
2
Inflammatory predictors of neurologic disability after preterm premature rupture of membranes.胎膜早破早产后脑神经功能障碍的炎症预测指标
Am J Obstet Gynecol. 2015 Feb;212(2):212.e1-9. doi: 10.1016/j.ajog.2014.09.016. Epub 2014 Sep 16.
3
Association between early administration of high-dose erythropoietin in preterm infants and brain MRI abnormality at term-equivalent age.早产儿早期给予高剂量促红细胞生成素与胎龄相当足月时脑 MRI 异常的相关性研究。
JAMA. 2014 Aug 27;312(8):817-24. doi: 10.1001/jama.2014.9645.
4
Circadian cycle-dependent EEG biomarkers of pathogenicity in adult mice following prenatal exposure to in utero inflammation.产前暴露于子宫内炎症的成年小鼠中致病性的昼夜节律依赖性脑电图生物标志物。
Neuroscience. 2014 Sep 5;275:305-13. doi: 10.1016/j.neuroscience.2014.06.022. Epub 2014 Jun 19.
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ALK5-dependent TGF-β signaling is a major determinant of late-stage adult neurogenesis.ALK5 依赖性 TGF-β 信号是晚期成年神经发生的主要决定因素。
Nat Neurosci. 2014 Jul;17(7):943-52. doi: 10.1038/nn.3732. Epub 2014 May 25.
6
Cognitive outcomes of preterm infants randomized to darbepoetin, erythropoietin, or placebo.早产儿随机分为达贝泊汀组、促红细胞生成素组和安慰剂组的认知结局。
Pediatrics. 2014 Jun;133(6):1023-30. doi: 10.1542/peds.2013-4307. Epub 2014 May 12.
7
Multi-modal assessment of long-term erythropoietin treatment after neonatal hypoxic-ischemic injury in rat brain.多模态评估新生大鼠脑缺氧缺血损伤后长期红细胞生成素治疗。
PLoS One. 2014 Apr 22;9(4):e95643. doi: 10.1371/journal.pone.0095643. eCollection 2014.
8
Maternal or neonatal infection: association with neonatal encephalopathy outcomes.母体或新生儿感染:与新生儿脑病结局的关系。
Pediatr Res. 2014 Jul;76(1):93-9. doi: 10.1038/pr.2014.47. Epub 2014 Apr 8.
9
Mechanisms of perinatal arterial ischemic stroke.围产期动脉缺血性卒中的发病机制。
J Cereb Blood Flow Metab. 2014 Jun;34(6):921-32. doi: 10.1038/jcbfm.2014.41. Epub 2014 Mar 26.
10
Neonatal peripheral immune challenge activates microglia and inhibits neurogenesis in the developing murine hippocampus.新生儿外周免疫刺激可激活发育中小鼠海马体中的小胶质细胞并抑制神经发生。
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炎症在围产期脑损伤中的作用。

The role of inflammation in perinatal brain injury.

作者信息

Hagberg Henrik, Mallard Carina, Ferriero Donna M, Vannucci Susan J, Levison Steven W, Vexler Zinaida S, Gressens Pierre

机构信息

1] Centre for the Developing Brain, Division of Imaging Sciences and Biomedical Engineering, King's College London, King's Health Partners, St Thomas' Hospital, London SE1 7EH, UK. [2] Perinatal Center, Institute of Physiology and Neurosciences and Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, 435 43 Gothenburg, Sweden.

Perinatal Center, Institute of Physiology and Neurosciences and Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, 435 43 Gothenburg, Sweden.

出版信息

Nat Rev Neurol. 2015 Apr;11(4):192-208. doi: 10.1038/nrneurol.2015.13. Epub 2015 Feb 17.

DOI:10.1038/nrneurol.2015.13
PMID:25686754
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4664161/
Abstract

Inflammation is increasingly recognized as being a critical contributor to both normal development and injury outcome in the immature brain. The focus of this Review is to highlight important differences in innate and adaptive immunity in immature versus adult brain, which support the notion that the consequences of inflammation will be entirely different depending on context and stage of CNS development. Perinatal brain injury can result from neonatal encephalopathy and perinatal arterial ischaemic stroke, usually at term, but also in preterm infants. Inflammation occurs before, during and after brain injury at term, and modulates vulnerability to and development of brain injury. Preterm birth, on the other hand, is often a result of exposure to inflammation at a very early developmental phase, which affects the brain not only during fetal life, but also over a protracted period of postnatal life in a neonatal intensive care setting, influencing critical phases of myelination and cortical plasticity. Neuroinflammation during the perinatal period can increase the risk of neurological and neuropsychiatric disease throughout childhood and adulthood, and is, therefore, of concern to the broader group of physicians who care for these individuals.

摘要

炎症越来越被认为是未成熟大脑正常发育和损伤结果的关键因素。本综述的重点是强调未成熟大脑与成人大脑在先天免疫和适应性免疫方面的重要差异,这支持了这样一种观点,即炎症的后果将因中枢神经系统发育的背景和阶段而完全不同。围产期脑损伤可由新生儿脑病和围产期动脉缺血性中风引起,通常发生在足月时,但也可发生在早产儿中。足月时,炎症在脑损伤之前、期间和之后发生,并调节脑损伤的易感性和发展。另一方面,早产通常是在非常早期的发育阶段接触炎症的结果,这不仅在胎儿期影响大脑,而且在新生儿重症监护环境中的出生后很长一段时间内也会影响大脑,影响髓鞘形成和皮质可塑性的关键阶段。围产期的神经炎症会增加儿童期和成年期患神经和神经精神疾病的风险,因此,这受到照顾这些个体的更广泛医生群体的关注。