Suppr超能文献

缺氧缺血与低温独立且交互影响短期恢复的新生仔猪的神经元病理学。

Hypoxia-Ischemia and Hypothermia Independently and Interactively Affect Neuronal Pathology in Neonatal Piglets with Short-Term Recovery.

机构信息

Department of Anesthesiology and Critical Care Medicine, Johns Hopkins University, Baltimore, Maryland, USA,

Department of Anesthesiology and Critical Care Medicine, Johns Hopkins University, Baltimore, Maryland, USA.

出版信息

Dev Neurosci. 2019;41(1-2):17-33. doi: 10.1159/000496602. Epub 2019 May 20.

Abstract

Therapeutic hypothermia is the standard of clinical care for moderate neonatal hypoxic-ischemic encephalopathy. We investigated the independent and interactive effects of hypoxia-ischemia (HI) and temperature on neuronal survival and injury in basal ganglia and cerebral cortex in neonatal piglets. Male piglets were randomized to receive HI injury or sham procedure followed by 29 h of normothermia, sustained hypothermia induced at 2 h, or hypothermia with rewarming during fentanyl-nitrous oxide anesthesia. Viable and injured neurons and apoptotic profiles were counted in the anterior putamen, posterior putamen, and motor cortex at 29 h after HI injury or sham procedure. Terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) identified genomic DNA fragmentation to confirm cell death. Though hypothermia after HI preserved viable neurons in the anterior and posterior putamen, hypothermia prevented neuronal injury in only the anterior putamen. Hypothermia initiated 2 h after injury did not protect against apoptotic cell death in either the putamen or motor cortex, and rewarming from hypothermia was associated with increased apoptosis in the motor cortex. In non-HI shams, sustained hypothermia during anesthesia was associated with neuronal injury and corresponding viable neuron loss in the anterior putamen and motor cortex. TUNEL confirmed increased neurodegeneration in the putamen of hypothermic shams. Anesthetized, normothermic shams did not show abnormal neuronal cytopathology in the putamen or motor cortex, thereby demonstrating minimal contribution of the anesthetic regimen to neuronal injury during normothermia. We conclude that the efficacy of hypothermic protection after HI is region specific and that hypothermia during anesthesia in the absence of HI may be associated with neuronal injury in the developing brain. Studies examining the potential interactions between hypothermia and anesthesia, as well as with longer durations of hypothermia, are needed.

摘要

治疗性低温是中重度新生儿缺氧缺血性脑病的临床治疗标准。我们研究了缺氧缺血(HI)和温度对新生仔猪基底节和大脑皮层神经元存活和损伤的独立和交互作用。雄性仔猪随机接受 HI 损伤或假手术,然后接受 29 小时的正常体温、2 小时开始的持续低温或芬太尼-氧化亚氮麻醉时的复温低温。HI 损伤或假手术后 29 小时,在前纹状体、后纹状体和运动皮层中计数存活和损伤神经元以及凋亡谱。末端脱氧核苷酸转移酶 dUTP 缺口末端标记(TUNEL)鉴定基因组 DNA 片段化以确认细胞死亡。尽管 HI 后低温保存了前纹状体和后纹状体中的存活神经元,但低温仅能预防前纹状体的神经元损伤。损伤后 2 小时开始的低温不能预防纹状体和运动皮层中的凋亡细胞死亡,而从低温复温与运动皮层中凋亡增加有关。在非 HI 假手术中,麻醉期间的持续低温与前纹状体和运动皮层的神经元损伤和相应的存活神经元丢失有关。TUNEL 证实了低温假手术纹状体中的神经退行性变增加。麻醉、正常体温的假手术未显示纹状体或运动皮层中神经元细胞病理学异常,从而证明在正常体温下麻醉方案对神经元损伤的影响很小。我们得出结论,HI 后低温保护的疗效具有区域特异性,并且在没有 HI 的情况下麻醉期间的低温可能与发育中大脑的神经元损伤有关。需要研究低温与麻醉之间以及与更长时间低温之间的潜在相互作用。

相似文献

2
White matter apoptosis is increased by delayed hypothermia and rewarming in a neonatal piglet model of hypoxic ischemic encephalopathy.
Neuroscience. 2016 Mar 1;316:296-310. doi: 10.1016/j.neuroscience.2015.12.046. Epub 2015 Dec 29.
4
Rewarming from therapeutic hypothermia induces cortical neuron apoptosis in a swine model of neonatal hypoxic-ischemic encephalopathy.
J Cereb Blood Flow Metab. 2015 May;35(5):781-93. doi: 10.1038/jcbfm.2014.245. Epub 2015 Jan 7.
7
Early antioxidant treatment and delayed hypothermia after hypoxia-ischemia have no additive neuroprotection in newborn pigs.
Anesth Analg. 2012 Sep;115(3):627-37. doi: 10.1213/ANE.0b013e31825d3600. Epub 2012 Jun 28.
10
Hypothermia is not therapeutic in a neonatal piglet model of inflammation-sensitized hypoxia-ischemia.
Pediatr Res. 2022 May;91(6):1416-1427. doi: 10.1038/s41390-021-01584-6. Epub 2021 May 28.

引用本文的文献

5
Plasma Biomarkers of Evolving Encephalopathy and Brain Injury in Neonates with Hypoxic-Ischemic Encephalopathy.
J Pediatr. 2023 Jan;252:146-153.e2. doi: 10.1016/j.jpeds.2022.07.046. Epub 2022 Aug 7.
7
Motor function and white matter connectivity in children cooled for neonatal encephalopathy.
Neuroimage Clin. 2021;32:102872. doi: 10.1016/j.nicl.2021.102872. Epub 2021 Nov 3.
9
[Research advances in the role of ferroptosis in neonatal hypoxic-ischemic brain damage].
Zhongguo Dang Dai Er Ke Za Zhi. 2021 May;23(5):536-541. doi: 10.7499/j.issn.1008-8830.2102045.

本文引用的文献

1
Proteasome Biology Is Compromised in White Matter After Asphyxic Cardiac Arrest in Neonatal Piglets.
J Am Heart Assoc. 2018 Oct 16;7(20):e009415. doi: 10.1161/JAHA.118.009415.
2
Limited benefit of slow rewarming after cerebral hypothermia for global cerebral ischemia in near-term fetal sheep.
J Cereb Blood Flow Metab. 2019 Nov;39(11):2246-2257. doi: 10.1177/0271678X18791631. Epub 2018 Aug 10.
3
4
Mild Neonatal Encephalopathy-How, When, and How Much to Treat?
JAMA Pediatr. 2018 Jan 1;172(1):3-4. doi: 10.1001/jamapediatrics.2017.3044.
5
Therapeutic hypothermia in mild neonatal encephalopathy: a national survey of practice in the UK.
Arch Dis Child Fetal Neonatal Ed. 2018 Jul;103(4):F388-F390. doi: 10.1136/archdischild-2017-313320. Epub 2017 Sep 23.
6
A validated clinical MRI injury scoring system in neonatal hypoxic-ischemic encephalopathy.
Pediatr Radiol. 2017 Oct;47(11):1491-1499. doi: 10.1007/s00247-017-3893-y. Epub 2017 Jun 16.
7
How long is sufficient for optimal neuroprotection with cerebral cooling after ischemia in fetal sheep?
J Cereb Blood Flow Metab. 2018 Jun;38(6):1047-1059. doi: 10.1177/0271678X17707671. Epub 2017 May 15.
8
10
Optimizing Cerebral Autoregulation May Decrease Neonatal Regional Hypoxic-Ischemic Brain Injury.
Dev Neurosci. 2017;39(1-4):248-256. doi: 10.1159/000452833. Epub 2016 Dec 16.

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