Edwards Adam B, Feindel Kirk W, Cross Jane L, Anderton Ryan S, Clark Vincent W, Knuckey Neville W, Meloni Bruno P
Perron Institute for Neurological and Translational Science, Nedlands, 6009, Western Australia, Australia; School of Health Sciences, The University of Notre Dame Australia, Fremantle, 6160, Western Australia, Australia; Department of Neurosurgery, Sir Charles Gardiner Hospital, QEII Medical Centre, Nedlands, 6009, Western Australia, Australia.
Centre for Microscopy, Characterisation and Analysis, The University of Western Australia, Nedlands, 6009, Western Australia, Australia.
J Neurosci Methods. 2017 Aug 15;288:62-71. doi: 10.1016/j.jneumeth.2017.06.016. Epub 2017 Jun 23.
The Rice-Vannucci model of hypoxic-ischaemic encephalopathy (HIE) has been associated with a high degree of variability with respect to the development of cerebral infarction and infarct lesion volume. For this reason, we examined the occurrence of communicational blood flow within the common carotid (CCA), internal (ICA), and external (ECA) carotid arteries following CCA occlusion as a source of variability in the model.
We propose a novel modification to the Rice-Vannucci model, whereby both the CCA and ECA are permanently ligated; mitigating communicational blood flow.
Using magnetic resonance angiography, phase-contrast velocity encoding, and pulsed arterial spin labelling, the modified Rice-Vannucci model (CCA/ECA occlusion) was demonstrated to mitigate communicational blood flow, whilst significantly reducing ipsilateral hemispherical cerebral blood flow (CBF). Comparatively, the original Rice-Vannucci model (CCA occlusion) demonstrated anterograde and retrograde blood flow within the ICA and CCA, respectively, with a non-significant reduction in ipsilateral CBF. Furthermore, CCA/ECA occlusion plus hypoxia (8% O/92% N; 2.5h) resulted in 100% of animals presenting with an infarct (vs 87%), significantly larger infarct volume at 48h (18.5% versus 10.0%; p<0.01), reduced standard deviation (±10% versus ±15%), and significantly worsened functional outcomes when compared to CCA occlusion plus hypoxia.
We compared a modified Rice-Vannucci model (CCA/ECA occlusion±hypoxia) to the commonly used Rice-Vannucci model (CCA occlusion±hypoxia).
This study demonstrates that CCA/ECA occlusion in the Rice-Vannucci model of HIE reduces infarct volume variability by limiting communicational blood flow.
缺氧缺血性脑病(HIE)的赖斯 - 万努奇模型在脑梗死的发生和梗死灶体积方面存在高度变异性。因此,我们研究了颈总动脉(CCA)闭塞后颈总动脉、颈内动脉(ICA)和颈外动脉(ECA)内交通血流的情况,将其作为该模型变异性的一个来源。
我们对赖斯 - 万努奇模型提出了一种新的改进方法,即永久性结扎CCA和ECA,以减少交通血流。
通过磁共振血管造影、相位对比速度编码和脉冲动脉自旋标记,改良的赖斯 - 万努奇模型(CCA/ECA闭塞)被证明可减少交通血流,同时显著降低同侧半球脑血流量(CBF)。相比之下,原始的赖斯 - 万努奇模型(CCA闭塞)在ICA和CCA内分别显示出顺行和逆行血流,同侧CBF无显著降低。此外,与CCA闭塞加缺氧相比,CCA/ECA闭塞加缺氧(8%O₂/92%N₂;2.5小时)导致100%的动物出现梗死(vs 87%),48小时时梗死体积显著更大(18.5%对10.0%;p<0.01),标准差降低(±10%对±15%),功能结局显著恶化。
我们将改良的赖斯 - 万努奇模型(CCA/ECA闭塞±缺氧)与常用的赖斯 - 万努奇模型(CCA闭塞±缺氧)进行了比较。
本研究表明,在HIE的赖斯 - 万努奇模型中,CCA/ECA闭塞通过限制交通血流降低了梗死体积变异性。