CB-17和SCID小鼠永久性脑缺血的可复制简单模型。

Akihiko Taguchi, Yukiko Kasahara, Takayuki Nakagomi, David M Stern, Mari Fukunaga, Makoto Ishikawa, Tomohiro Matsuyama
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引用次数: 58

摘要

为了评估新的脑卒中治疗方法,有必要利用一个高度可重复的局灶性脑缺血模型。尽管文献中采用了一系列啮齿动物中风模型,但由于存在相当大的动物间和实验室间差异,因此关于缺血区可重复性的问题一直存在。我们开发了一种高度可重复的中风模型,该模型涉及SCID (CB-17/lcr- SCID /scidJcl)和CB-17 (CB-17/lcr-+/+Jcl)小鼠的MCA直接电凝。通过对Tamura方法的改进,我们的研究结果表明,SCID和CB-17小鼠在慢性期(长达180天)具有较高的可重复性皮质梗死存活率,而C57BL/6小鼠则没有。我们相信我们的临床前模型代表了测试未来可能适用于中风患者的治疗方法的一步。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Reproducible and Simple Model of Permanent Cerebral Ischemia in CB-17 and SCID Mice.

A Reproducible and Simple Model of Permanent Cerebral Ischemia in CB-17 and SCID Mice.

A Reproducible and Simple Model of Permanent Cerebral Ischemia in CB-17 and SCID Mice.

A Reproducible and Simple Model of Permanent Cerebral Ischemia in CB-17 and SCID Mice.

In order to evaluate novel stroke therapies, it is essential to utilize a highly reproducible model of focal cerebral ischemia. Though a range of rodent stroke models has been employed in the literature, there are persistent issues regarding reproducibility of the ischemic zone, as there is considerable inter-animal and inter-laboratory variation. We have developed a highly reproducible model of stroke that involves direct electrocoagulation of the MCA in SCID (CB-17/lcr-scid/scidJcl) and CB-17 (CB-17/lcr-+/+Jcl) mice. Using a modification of the Tamura method, our results demonstrate reproducible cortical infarction with high survival in the chronic period (up to 180 days) in SCID and CB-17, but not in C57BL/6, mice. We believe that our preclinical model represents a step forward for testing future therapeutic methods potentially applicable to patients with stroke.

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