Nowak Błażej, Holak Piotr, Małysz-Cymborska Izabela, Chovsepian Alexandra, Dening Yanina, Olszewski Jarosław, Piecuch Aleksandra, Jasieniak Maria, Jasieniak Jakub, Szterk Arkadiusz, Sady Maria, Ferenc Karolina, Berchtold Daniel, Jabłoński Artur, Zabielski Romuald, Gajewski Zdzisław, Magnus Tim, Janowski Mirosław, Walczak Piotr, Meisel Andreas, Pan-Montojo Francisco, Gołubczyk Dominika
Division of Interventional Neuroradiology, Department of Radiology, The National Medical Institute of the Ministry of the Interior and Administration, Warsaw, Poland.
Department of Surgery and Roentgenology With a Clinic, Faculty of Veterinary Medicine, University of Warmia and Mazury in Olsztyn, Olsztyn, Poland.
Front Neurosci. 2025 Jun 5;19:1572925. doi: 10.3389/fnins.2025.1572925. eCollection 2025.
Stroke is a leading cause of death and long-term disability. Pigs have been considered an ideal large animal model in biomedicine; however, the complex vascular anatomy has posed challenges for stroke research. Nonetheless, we have previously overcome these limitations and demonstrated the feasibility of endovascularly inducing stroke in pigs. Here, we study to further mimic clinical situation by achieving recanalization, which has not been previously accomplished.
A stroke was induced in eight juvenile male domestic pigs. In anaestethised animals catheter was placed in the ascending pharyngeal artery near the rete mirabile (RM) under X-ray guidance. The animals were then transferred to an MRI scanner. Gadolinium-based contrast agent (GBCA) was infused at various speeds until transcatheter cerebral perfusion was visible on MRI. Subsequently, a mixture of thrombin and GBCA was infused, and the retention of contrast on MRI scans proved successful induction of thrombosis. Subsequent DWI and PWI MR images confirmed the successful induction of stroke. Two hours after ischemia, we intra-arterially infused rtPA (20 mg) and confirmed recanalization of the thrombosed vessels using MRI. One month later the stroke was confirmed through follow-up MRI scans and post-mortem histological and immunohistochemical analyses.
We successfully induced stroke with an average lesion size based on ADC at 8.18 ± 4.98 cm, ranging from 3.27 to 17.33 cm. After recanalization, the severely hypoperfused area (Tmax>6) was only 1.168 ± 0.223 cm. Subsequent histological analysis revealed neuronal loss within the lesion, the formation of astrocytic scar tissue, and elevated levels of activated microglia.
Our study demonstrates the successful recanalization of cerebral vasculature in porcine model of ischemic stroke. It makes the model highly relevant to the current clinical workflow and offers an attractive avenue for studying novel diagnostics, therapeutics and further exploration of the underlying pathomechanisms. The feasibility of continuous MR imaging throughout the entire procedure facilitates the achievement of the aforementioned goals more readily.
中风是导致死亡和长期残疾的主要原因。猪被认为是生物医学中理想的大型动物模型;然而,复杂的血管解剖结构给中风研究带来了挑战。尽管如此,我们之前已经克服了这些限制,并证明了在猪体内通过血管内诱导中风的可行性。在此,我们进行研究以通过实现再通来进一步模拟临床情况,这在之前尚未完成。
对八只幼年雄性家猪诱导中风。在麻醉的动物中,在X射线引导下将导管置于靠近奇网(RM)的咽升动脉中。然后将动物转移到MRI扫描仪。以不同速度注入钆基造影剂(GBCA),直到在MRI上可见经导管脑灌注。随后,注入凝血酶和GBCA的混合物,MRI扫描上造影剂的滞留证明血栓形成诱导成功。随后的扩散加权成像(DWI)和灌注加权成像(PWI)MR图像证实中风诱导成功。缺血两小时后,我们动脉内注入重组组织型纤溶酶原激活剂(rtPA,20mg),并使用MRI确认血栓形成血管的再通。一个月后,通过后续的MRI扫描以及死后组织学和免疫组织化学分析确认中风。
我们成功诱导了中风,基于表观扩散系数(ADC)的平均病变大小为8.18±4.98cm,范围为3.27至17.33cm。再通后,严重灌注不足区域(Tmax>6)仅为1.168±0.223cm。随后的组织学分析显示病变内神经元丢失、星形胶质细胞瘢痕组织形成以及活化小胶质细胞水平升高。
我们的研究证明了在缺血性中风猪模型中脑脉管系统的成功再通。这使得该模型与当前临床工作流程高度相关,并为研究新型诊断方法、治疗方法以及进一步探索潜在病理机制提供了有吸引力的途径。在整个过程中进行连续MR成像的可行性有助于更轻松地实现上述目标。