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Endovascular ischemic stroke models of adult rhesus monkeys: a comparison of two endovascular methods

To further investigate and improve upon current stroke models in nonhuman primates, infarct size, neurologic function and survival were evaluated in two endovascular ischemic models in sixteen rhesus monkeys. The first method utilized a micro-catheter or an inflatable balloon to occlude the M1 segme...

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Published in:Scientific reports 2016-08, Vol.6 (1), p.31608-31608, Article 31608
Main Authors: Wu, Di, Chen, Jian, Wang, Bincheng, Zhang, Mo, Shi, Jingfei, Ma, Yanhui, Zhu, Zixin, Yan, Feng, He, Xiaoduo, Li, Shengli, Dornbos III, David, Ding, Yuchuan, Ji, Xunming
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Language:English
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Summary:To further investigate and improve upon current stroke models in nonhuman primates, infarct size, neurologic function and survival were evaluated in two endovascular ischemic models in sixteen rhesus monkeys. The first method utilized a micro-catheter or an inflatable balloon to occlude the M1 segment in six monkeys. In the second model, an autologous clot was injected via a micro-catheter into the M1 segment in ten monkeys. MRI scanning was performed on all monkeys both at baseline and 3 hours after the onset of ischemia. Spetzler neurologic functions were assessed post-operatively, and selective perfusion deficits were confirmed by DSA and MRI in all monkeys. Animals undergoing micro-catheter or balloon occlusion demonstrated more profound hemiparesis, larger infarct sizes, lower Spetzler neurologic scores and increased mortality compared to the thrombus occlusion group. In animals injected with the clot, there was no evidence of dissolution, and the thrombus was either near the injection site (M1) or flushed into the superior division of the MCA (M2). All animals survived the M2 occlusion. M1 occlusion with thrombus generated 50% mortality. This study highlighted clinically important differences in these two models, providing a platform for further study of a translational thromboembolic model of acute ischemic stroke.
ISSN:2045-2322
2045-2322
DOI:10.1038/srep31608