Chen C, Wang Q, Gao Y, Lu Z, Cui X, Zheng T, Liu Y, Li X, He X, Zhang X, Duan C, Li T
The National Key Clinical Specialty, The Engineering Technology Research Center of Education Ministry of China, Guangdong Provincial Key Laboratory on Brain Function Repair and Regeneration, Department of Neurosurgery, Zhujiang Hospital, Southern Medical University, Guangzhou 510282, China.
The National Key Clinical Specialty, The Engineering Technology Research Center of Education Ministry of China, Guangdong Provincial Key Laboratory on Brain Function Repair and Regeneration, Department of Neurosurgery, Zhujiang Hospital, Southern Medical University, Guangzhou 510282, China.
Neuroscience. 2015 Oct 15;306:39-49. doi: 10.1016/j.neuroscience.2015.08.020. Epub 2015 Aug 20.
Cerebral venous sinus thrombosis (CVST) is a rare but life-threatening disease and an animal model for in-depth study of CVST is needed. This study aimed to develop a rat model suitable for studying clinically relevant aspects of CVST and investigating its dynamic pathophysiological changes during a 7-day period.
A photothrombosis method was used to create a rat sinus-vein thrombosis model. A spot size-adjustable Diode Pumped Solid State laser (DPSS) combined with thrombin injection occluded the rostral and caudal superior sagittal sinus (SSS). The model was used to evaluate pathophysiological changes at different time points over 7 days. Evans Blue dye injection was used to detect alterations in blood-brain barrier (BBB) permeability. Brain water content was also measured. Moreover, we examined changes in brain infarct volume, neurological function, as well as histology after induction of CVST.
CVST in rats significantly altered BBB permeability, consistent with the development of brain edema. It was accompanied by an increase in brain infarct volume and deficits in neurological function that began on day 1, peaked on day 2, and typically improved by day 7 due to the neuroprotective effects of angiogenesis and gliocyte proliferation.
In this study, we describe a rat model that produces clinically relevant pathophysiology and pathology that will facilitate evaluation of therapeutic regimens for CVST. Furthermore, our results indicate a period of optimal clinical intervention for patients with CVST, which may reduce the probability of dependency and death.
脑静脉窦血栓形成(CVST)是一种罕见但危及生命的疾病,需要一种用于深入研究CVST的动物模型。本研究旨在建立一种适合研究CVST临床相关方面并调查其在7天内动态病理生理变化的大鼠模型。
采用光血栓形成法建立大鼠静脉窦血栓形成模型。使用光斑尺寸可调的二极管泵浦固体激光器(DPSS)结合凝血酶注射闭塞大鼠上矢状窦(SSS)的头端和尾端。该模型用于评估7天内不同时间点的病理生理变化。通过注射伊文思蓝染料检测血脑屏障(BBB)通透性的改变。还测量了脑含水量。此外,我们检查了CVST诱导后脑梗死体积、神经功能以及组织学的变化。
大鼠CVST显著改变了BBB通透性,这与脑水肿的发展一致。它伴随着脑梗死体积增加和神经功能缺陷,这些变化在第1天开始出现,在第2天达到峰值,由于血管生成和胶质细胞增殖的神经保护作用,通常在第7天有所改善。
在本研究中,我们描述了一种产生临床相关病理生理和病理变化的大鼠模型,这将有助于评估CVST的治疗方案。此外,我们的结果表明了CVST患者最佳临床干预的时间段,这可能会降低依赖和死亡的概率。