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内皮素与小儿创伤性脑损伤中的神经血管单元

Endothelin and the neurovascular unit in pediatric traumatic brain injury.

作者信息

Armstead William M, Raghupathi Ramesh

机构信息

Department of Anesthesiology and Critical Care and Department of Pharmacology, University of Pennsylvania, Philadelphia, PA 19104, USA.

出版信息

Neurol Res. 2011 Mar;33(2):127-32. doi: 10.1179/016164111X12881719352138.

Abstract

OBJECTIVE

This study characterized the association between endothelin-1, cerebral hemodynamics, and histopathology after fluid percussion brain injury in the newborn pig.

METHODS

Lateral fluid percussion injury was induced in newborn pigs equipped with a closed cranial window. Cerebral blood flow was determined with radiolabeled microspheres and cerebrospinal fluid endothelin-1 was measured by radioimmunoassay.

RESULTS

Cerebrospinal fluid endothelin-1 was increased from 26±4 to 296±37 pg/ml (∼10(-10) M) at 8 hours following fluid percussion injury. Post-injury treatment (30 minutes) with the endothelin-1 antagonist BQ-123 (1 mg/kg, intravenous) blocked pial artery vasoconstriction to topical endothelin-1 (∼10(-10) M) and blunted fluid percussion injury-induced reductions in cerebral blood flow at 8 hours post-insult (56±6 and 26±4 ml/minute versus 57±6 and 40± ml/minute; 100 g for cerebral blood flow before injury and 8 hours post-fluid percussion injury in vehicle and BQ-123 post-treated animals, respectively). Fluid percussion injury resulted in neuronal cell loss and decreased microtubule associated protein 2 immunoreactivity in the parietal cortex, which were blunted by BQ-123.

DISCUSSION

These data indicate that fluid percussion injury-induced changes in cerebral hemodynamics are associated with neuronal damage and that endothelin-1 contributes to fluid percussion injury-induced histopathologic changes.

摘要

目的

本研究描述了新生猪液体冲击脑损伤后内皮素-1、脑血流动力学和组织病理学之间的关联。

方法

对配备闭合颅骨视窗的新生猪进行侧方液体冲击损伤。用放射性微球测定脑血流量,并用放射免疫分析法测量脑脊液内皮素-1。

结果

液体冲击损伤后8小时,脑脊液内皮素-1从26±4 pg/ml(约10⁻¹⁰ M)增加至296±37 pg/ml。损伤后用内皮素-1拮抗剂BQ-123(1 mg/kg,静脉注射)治疗30分钟,可阻断软脑膜动脉对局部内皮素-1(约10⁻¹⁰ M)的收缩反应,并减轻液体冲击损伤诱导的伤后8小时脑血流量减少(分别为56±6和26±4 ml/分钟,而对照组为57±6和40± ml/分钟;损伤前及液体冲击损伤后8小时,对照组和BQ-123治疗组猪的脑血流量均以100 g脑组织计算)。液体冲击损伤导致顶叶皮质神经元细胞丢失和微管相关蛋白2免疫反应性降低,而BQ-123可减轻这些变化。

讨论

这些数据表明,液体冲击损伤诱导的脑血流动力学变化与神经元损伤相关,且内皮素-1促成了液体冲击损伤诱导的组织病理学变化。

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