The first endovascular rat glioma model for pre-clinical evaluation of intra-arterial therapeutics.

IF 2.1 4区 医学 Q3 Medicine
Interventional Neuroradiology Pub Date : 2025-08-01 Epub Date: 2023-05-08 DOI:10.1177/15910199231169597
Jaims Lim, Ammad A Baig, Brianna M Donnelly, Lee D Chaves, Suyog U Pol, Carmon Koenigsknecht, Donald Pionessa, Bennett R Levy, Liza Gutierrez, Vincent M Tutino, Elad I Levy, Adnan H Siddiqui
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引用次数: 0

Abstract

BackgroundSeveral translational animal models have been described assessing intra-arterial (IA) treatments for malignant gliomas. We describe the first endovascular animal model that allows testing of IA drug delivery as a first-line treatment, which is difficult to do in actual patients. We report a unique protocol for vascular access and IA delivery in the rat model that, unlike prior reports, does not require direct puncture and opening of proximal cerebrovasculature which carries risk of ischemia in the animal brain post-delivery.MethodsWistar rats underwent left femoral artery catherization with a Balt Magic 1.2F catheter or Marathon Flow directed 1.5F Microcatheter with an Asahi Chikai 0.008 micro-guidewire which was navigated to the left internal carotid artery under x-ray. 25% mannitol was administered to test blood brain barrier breakdown (BBBB). Additional rats were implanted with C6 glioma cells in the left frontal lobe. C6 Glioma-Implanted Rats (C6GRs) were monitored for overall survival and tumor growth. Tumor volumes from MRI images were calculated utilizing 3D slicer. Additional rats underwent femoral artery catheterization with Bevacizumab, carboplatin, or irinotecan injected into the left internal carotid artery to test feasibility and safety.ResultsA successful endovascular access and BBBB protocol was established. BBBB was confirmed with positive Evans blue staining. 10 rats were successfully implanted with C6 gliomas with confirmed growths on MRI. Overall survival was 19.75 ± 2.21 days. 5 rats were utilized for the development of our femoral catheterization protocol and BBBB testing. With regards to IA chemotherapy dosage testing, control rats tolerated targeted 10 mg/kg of bevascizumab, 2.4 mg/kg of carboplatin, and 15 mg/kg of irinotecan IA ICA injections without any complications.ConclusionsWe present the first endovascular IA rat glioma model that allows selective catheterization of the intracranial vasculature and assessment of IA therapies for gliomas without need for access and sacrifice of proximal cerebrovasculature.

第一个血管内大鼠胶质瘤模型用于动脉内治疗的临床前评估。
研究背景:一些动物模型已经被用来评估动脉内治疗恶性胶质瘤的效果。我们描述了第一个血管内动物模型,允许测试IA药物递送作为一线治疗,这在实际患者中很难做到。我们报告了一种独特的大鼠模型血管通路和IA递送方案,与先前的报道不同,该方案不需要直接穿刺和打开近端脑血管,这有可能导致动物大脑在分娩后缺血。方法采用Balt Magic 1.2F导管或Marathon Flow - directed 1.5F微导管与Asahi Chikai 0.008微导丝在x线下引导至左颈内动脉。给予25%甘露醇检测血脑屏障破坏(BBBB)。另外在左额叶植入C6胶质瘤细胞。观察C6胶质瘤植入大鼠(C6GRs)的总生存率和肿瘤生长情况。利用三维切片机计算MRI图像的肿瘤体积。另外对大鼠进行股动脉插管,将贝伐单抗、卡铂或伊立替康注射到左颈内动脉,以测试其可行性和安全性。结果成功建立了血管内通路和BBBB方案。Evans蓝染色阳性证实BBBB。10只大鼠成功植入C6胶质瘤,MRI证实其生长。总生存期19.75±2.21天。5只大鼠用于我们的股动脉插管方案的制定和血脑屏障测试。在IA化疗剂量试验方面,对照大鼠耐受靶向贝伐珠单抗10 mg/kg、卡铂2.4 mg/kg、伊立替康15 mg/kg的IA ICA注射,无并发症。我们提出了第一个血管内IA大鼠胶质瘤模型,该模型可以在不需要进入和牺牲近端脑血管的情况下,对颅内血管进行选择性导管置入,并评估IA治疗胶质瘤的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.80
自引率
11.80%
发文量
192
审稿时长
6-12 weeks
期刊介绍: Interventional Neuroradiology (INR) is a peer-reviewed clinical practice journal documenting the current state of interventional neuroradiology worldwide. INR publishes original clinical observations, descriptions of new techniques or procedures, case reports, and articles on the ethical and social aspects of related health care. Original research published in INR is related to the practice of interventional neuroradiology...
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