Kainth Daraspreet, Salazar Pascal, Safinia Cyrus, Chow Ricky, Bachour Ornina, Andalib Sasan, McKinney Alexander M, Divani Afshin A
Department of Neurosurgery, University of Minnesota, Minneapolis, MN, USA.
Vital Images, Minnetonka, MN, USA.
J Vasc Interv Neurol. 2017 Jan;9(3):26-35.
Rabbit models of intracranial aneurysms are frequently used in pre-clinical settings. This study aimed to demonstrate an alternative, extravascular method for creating elastase-induced aneurysms, and how ligation of the right common carotid arteries (RCCA) can impact flow redistribution into left CCA (LCCA).
Elastase-induced aneurysms in 18 New Zealand rabbits (4.14 ± 0.314 kg) were created by applying 3-5 U of concentrated elastase solution to the exterior of the right and left CCA roots (RCCA and LCCA). After the induction of the aneurysm, the aneurysm was either kept intact to the rest of the corresponding CCA, severed from the rest of the CCA to allow for a free standing aneurysm, or was anchored to nearby tissue to influence the angle and orientation of the aneurysm with respect to the parent vessel. Ultrasound studies were performed before and after creation of aneurysms to collect blood flow measurements inside the aneurysm pouch and surrounding arteries. Prior to sacrificing the animals, computed tomography angiography studies were performed. Harvested aneurysmal tissues were used for histological analysis.
Elastase-induced aneurysms were successfully created by the extravascular approach. Histological studies showed that the biological response was similar to human cerebral aneurysms and previously published elastase-induced rabbit aneurysm models. Ultrasound measurements indicated that after the RCCA was ligated, blood flow significantly increased in the LCCA at one-month follow-up.
An alternate method for creating elastase-induced aneurysms has been demonstrated. The novel aspects of our method allow for ligation of one or both common carotid arteries to create a single or bilateral aneurysm with an ability to control the orientation of the induced aneurysm.
颅内动脉瘤的兔模型常用于临床前研究。本研究旨在展示一种通过血管外方法创建弹性蛋白酶诱导的动脉瘤,以及结扎右侧颈总动脉(RCCA)如何影响血流重新分布至左侧颈总动脉(LCCA)。
对18只新西兰兔(体重4.14±0.314千克)通过在右侧和左侧颈总动脉根部(RCCA和LCCA)外部涂抹3 - 5单位浓缩弹性蛋白酶溶液来创建弹性蛋白酶诱导的动脉瘤。动脉瘤诱导后,要么使其与相应颈总动脉的其余部分保持完整,要么从颈总动脉的其余部分切断以形成独立的动脉瘤,要么将其固定在附近组织上以影响动脉瘤相对于母血管的角度和方向。在创建动脉瘤前后进行超声研究,以收集动脉瘤囊袋和周围动脉内的血流测量数据。在处死动物之前,进行计算机断层血管造影研究。收获的动脉瘤组织用于组织学分析。
通过血管外方法成功创建了弹性蛋白酶诱导的动脉瘤。组织学研究表明,生物学反应与人类脑动脉瘤以及先前发表的弹性蛋白酶诱导的兔动脉瘤模型相似。超声测量表明,结扎RCCA后,在1个月随访时LCCA中的血流显著增加。
已展示了一种创建弹性蛋白酶诱导的动脉瘤的替代方法。我们方法的新颖之处在于能够结扎一侧或双侧颈总动脉以创建单个或双侧动脉瘤,并能够控制诱导动脉瘤的方向。