Megyesi J F, Vollrath B, Cook D A, Findlay J M
Department of Surgery, University of Alberta, Edmonton, Canada.
Neurosurgery. 2000 Feb;46(2):448-60; discussion 460-1.
Cerebral vasospasm is delayed-onset cerebral arterial narrowing in response to blood clots left in the subarachnoid space after spontaneous aneurysmal subarachnoid hemorrhage (SAH). Ideally, studies on the pathogenesis and treatment of cerebral vasospasm in humans should be conducted using human cerebral arteries. Because in vivo experiments using human vessels are not possible, and postmortem pathological examination of human arteries in vasospasm provides only a limited amount of information, a number of animal models of vasospasm have been developed.
The literature was searched to find all references to in vivo animal models of SAH and vasospasm. An online search of the medical database MEDLINE was initially performed using the key words "cerebral," "vasospasm," "subarachnoid," "hemorrhage," "animal," and "model." References were checked to determine the first description of each in vivo animal model.
Fifty-seven models of SAH and vasospasm were identified. These models used one of three techniques to simulate SAH: 1) an artery was punctured allowing blood to escape and collect around the artery and its neighbors; 2) an artery was surgically exposed, and autologous blood obtained from another site was placed around the artery; or 3) blood from another site was injected into the subarachnoid space and was allowed to collect around arteries. Each technique has advantages and disadvantages. The majority of animal models of SAH and vasospasm use intracranial arteries; however, extracranial arteries have also been used recently in vasospasm experiments. These studies seem easier and less costly to perform, but concerns exist regarding the physiological dissimilarity between systemic and cerebral arteries.
The model of SAH and vasospasm used most frequently is the canine "two-hemorrhage" model, in which two injections of blood into the dog's basal cistern performed 48 hours apart result in greater arterial vasoconstriction than that effected by a single injection of blood. On the basis of its ability to accurately predict what occurs in human SAH, the best model of vasospasm seems to be the primate model in which a blood clot is surgically placed around the large cerebral vessels at the base of the monkey's brain.
脑血管痉挛是自发性动脉瘤性蛛网膜下腔出血(SAH)后,因蛛网膜下腔残留血凝块而导致的迟发性脑动脉狭窄。理想情况下,关于人类脑血管痉挛发病机制和治疗的研究应使用人类脑动脉进行。由于无法进行使用人类血管的体内实验,且对处于血管痉挛状态的人类动脉进行尸检病理检查提供的信息有限,因此已开发出多种血管痉挛动物模型。
检索文献以查找所有关于SAH和血管痉挛体内动物模型的参考文献。最初使用关键词“脑”“血管痉挛”“蛛网膜下腔”“出血”“动物”和“模型”对医学数据库MEDLINE进行在线搜索。检查参考文献以确定每种体内动物模型的首次描述。
共识别出57种SAH和血管痉挛模型。这些模型使用三种技术之一来模拟SAH:1)穿刺动脉,使血液逸出并在动脉及其周围聚集;2)手术暴露动脉,并将从另一部位获取的自体血置于动脉周围;或3)将来自另一部位的血液注入蛛网膜下腔,并使其在动脉周围聚集。每种技术都有优缺点。大多数SAH和血管痉挛动物模型使用颅内动脉;然而,颅外动脉最近也被用于血管痉挛实验。这些研究似乎更容易进行且成本更低,但对于体循环动脉和脑动脉之间的生理差异存在担忧。
最常使用的SAH和血管痉挛模型是犬“两次出血”模型,即每隔48小时向犬的基底池注射两次血液,与单次注射血液相比,会导致更大程度的动脉血管收缩。基于其准确预测人类SAH中发生情况的能力,最佳的血管痉挛模型似乎是灵长类动物模型,即在猴子脑底部的大脑大血管周围手术放置血凝块。