Suppr超能文献

促红细胞生成素作为新生儿脑损伤的神经保护剂:动物模型

Erythropoietin as a neuroprotectant for neonatal brain injury: animal models.

作者信息

Traudt Christopher M, Juul Sandra E

机构信息

Division of Neonatology, Department of Pediatrics, University of Washington, Seattle, WA, USA.

出版信息

Methods Mol Biol. 2013;982:113-26. doi: 10.1007/978-1-62703-308-4_7.

Abstract

Prematurity and perinatal hypoxia-ischemia are common problems that result in significant neurodevelopmental morbidity and high mortality worldwide. The Vannucci model of unilateral brain injury was developed to model perinatal brain injury due to hypoxia-ischemia. Because the rodent brain is altricial, i.e., it develops postnatally, investigators can model either preterm or term brain injury by varying the age at which injury is induced. This model has allowed investigators to better understand developmental changes that occur in susceptibility of the brain to injury, evolution of brain injury over time, and response to potential neuroprotective treatments. The Vannucci model combines unilateral common carotid artery ligation with a hypoxic insult. This produces injury of the cerebral cortex, basal ganglia, hippocampus, and periventricular white matter ipsilateral to the ligated artery. Varying degrees of injury can be obtained by varying the depth and duration of the hypoxic insult. This chapter details one approach to the Vannucci model and also reviews the neuroprotective effects of erythropoietin (Epo), a neuroprotective treatment that has been extensively investigated using this model and others.

摘要

早产和围产期缺氧缺血是常见问题,在全球范围内会导致严重的神经发育疾病和高死亡率。单侧脑损伤的Vannucci模型是为模拟缺氧缺血所致围产期脑损伤而建立的。由于啮齿动物的大脑是晚成的,即出生后才发育,研究人员可以通过改变诱导损伤的年龄来模拟早产或足月脑损伤。该模型使研究人员能够更好地了解大脑对损伤易感性的发育变化、脑损伤随时间的演变以及对潜在神经保护治疗的反应。Vannucci模型将单侧颈总动脉结扎与缺氧刺激相结合。这会导致结扎动脉同侧的大脑皮质、基底神经节、海马体和脑室周围白质受损。通过改变缺氧刺激的深度和持续时间,可以获得不同程度的损伤。本章详细介绍了一种建立Vannucci模型的方法,还综述了促红细胞生成素(Epo)的神经保护作用,促红细胞生成素是一种神经保护治疗药物,已使用该模型及其他模型进行了广泛研究。

相似文献

1
Erythropoietin as a neuroprotectant for neonatal brain injury: animal models.
Methods Mol Biol. 2013;982:113-26. doi: 10.1007/978-1-62703-308-4_7.
4
Magnesium sulphate induces preconditioning in preterm rodent models of cerebral hypoxia-ischemia.
Int J Dev Neurosci. 2018 Nov;70:56-66. doi: 10.1016/j.ijdevneu.2018.01.002. Epub 2018 Feb 3.
5
Erythropoietin exerts neuroprotective effect in neonatal rat model of hypoxic-ischemic brain injury.
Brain Dev. 2003 Oct;25(7):494-8. doi: 10.1016/s0387-7604(03)00039-1.
6
Neuroprotective effect of the peptides ADNF-9 and NAP on hypoxic-ischemic brain injury in neonatal rats.
Brain Res. 2006 Oct 18;1115(1):169-78. doi: 10.1016/j.brainres.2006.07.114. Epub 2006 Aug 30.
7
Neuroprotective effects of N-acetylaspartylglutamate in a neonatal rat model of hypoxia-ischemia.
Eur J Pharmacol. 2002 Feb 22;437(3):139-45. doi: 10.1016/s0014-2999(02)01289-x.
9
Effects of erythropoietin on neonatal hypoxia-ischemia brain injury in rat model.
Physiol Behav. 2017 Feb 1;169:74-81. doi: 10.1016/j.physbeh.2016.11.029. Epub 2016 Nov 23.

引用本文的文献

3
Trial of Erythropoietin for Hypoxic-Ischemic Encephalopathy in Newborns.
N Engl J Med. 2022 Jul 14;387(2):148-159. doi: 10.1056/NEJMoa2119660.
4
Neuroprotective effects of Sonic hedgehog agonist SAG in a rat model of neonatal stroke.
Pediatr Res. 2021 Dec;90(6):1161-1170. doi: 10.1038/s41390-021-01408-7. Epub 2021 Mar 2.
5
Protective effect of adenovirus-mediated erythropoietin expression on the spiral ganglion neurons in the rat inner ear.
Int J Mol Med. 2018 May;41(5):2669-2677. doi: 10.3892/ijmm.2018.3455. Epub 2018 Feb 5.
7
[Relationship between serum erythropoietin levels and brain injury in preterm infants].
Zhongguo Dang Dai Er Ke Za Zhi. 2016 Oct;18(10):947-952. doi: 10.7499/j.issn.1008-8830.2016.10.006.
8
Pharmacotherapy for Neonatal Seizures: Current Knowledge and Future Perspectives.
Drugs. 2016 Apr;76(6):647-61. doi: 10.1007/s40265-016-0554-7.
9
Controversies in preterm brain injury.
Neurobiol Dis. 2016 Aug;92(Pt A):90-101. doi: 10.1016/j.nbd.2015.10.012. Epub 2015 Oct 23.
10
Serial plasma metabolites following hypoxic-ischemic encephalopathy in a nonhuman primate model.
Dev Neurosci. 2015;37(2):161-71. doi: 10.1159/000370147. Epub 2015 Feb 27.

本文引用的文献

1
Pharmacological neuroprotection after perinatal hypoxic-ischemic brain injury.
Curr Neuropharmacol. 2010 Dec;8(4):324-34. doi: 10.2174/157015910793358150.
2
Erythropoietin for neonatal brain injury: opportunity and challenge.
Int J Dev Neurosci. 2011 Oct;29(6):583-91. doi: 10.1016/j.ijdevneu.2010.12.007. Epub 2011 Jan 28.
4
Cerebellum of the premature infant: rapidly developing, vulnerable, clinically important.
J Child Neurol. 2009 Sep;24(9):1085-104. doi: 10.1177/0883073809338067.
5
Erythropoietin sustains cognitive function and brain volume after neonatal stroke.
Dev Neurosci. 2009;31(5):403-11. doi: 10.1159/000232558. Epub 2009 Aug 11.
6
Erythropoietin improved neurologic outcomes in newborns with hypoxic-ischemic encephalopathy.
Pediatrics. 2009 Aug;124(2):e218-26. doi: 10.1542/peds.2008-3553. Epub 2009 Jul 27.
7
Erythropoietin-receptor gene regulation in neuronal cells.
Pediatr Res. 2009 Jun;65(6):619-24. doi: 10.1203/PDR.0b013e31819ea3b8.
8
Neonatal stress or morphine treatment alters adult mouse conditioned place preference.
Neonatology. 2009;95(3):230-9. doi: 10.1159/000165379. Epub 2008 Oct 27.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验