Armstead William M, Raghupathi Ramesh
Department of Anesthesiology and Critical Care and Department of Pharmacology, University of Pennsylvania, Philadelphia, PA 19104, USA.
Neurol Res. 2011 Mar;33(2):127-32. doi: 10.1179/016164111X12881719352138.
This study characterized the association between endothelin-1, cerebral hemodynamics, and histopathology after fluid percussion brain injury in the newborn pig.
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.
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.
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.
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。
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。
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。
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。