Stem Cell Res Ther. 2013;4(5):116. doi: 10.1186/scrt327.
Rat middle cerebral artery occlusion (MCAO) model is the most commonly used animal model in ischemic stroke studies. In the model, to increase the amount of stem cells or drugs to enter the brain after delivery into the internal carotid artery (ICA), the pterygopalatine artery (PPA) is occluded. However, PPA occlusion is a technically demanding procedure which often causes complications.
In this study, we developed an ICA injection needle to facilitate easy and efficient delivery of stem cells to the ischemic brain through the ICA without the need of PPA occlusion. We injected methylene blue and fluorescence dye DiI-labeled human mesenchymal stem cells (DiI-hMSCs) into the ICA in rats with the ICA injection needle (without PPA ligation) or the conventional micro-injection needle (with PPA ligation) and assessed their distributions.
When methylene blue was injected, evident blue stains were found in the brain of the injection side particularly the middle cerebral artery (MCA)-supplied areas but not in the PPA supplied areas. Similarly, when DiI-hMSCs were injected, the cells largely appeared in the MCA-supplied tissues, which were similar in quantity compared to conventional micro-injection needle injection with PPA occlusion. Moreover, hMSCs injected with the ICA needle or the micro-injection needle similarly improved the functional recovery of the infarcted brain.
Our results indicate that the ICA injection needle is easy to use and efficient in delivering cells to the ischemic brain tissue in rat MCAO model.
大鼠大脑中动脉闭塞(MCAO)模型是缺血性脑卒中研究中最常用的动物模型。在该模型中,为了增加干细胞或药物在经颈内动脉(ICA)给药后进入大脑的量,通常会闭塞翼腭动脉(PPA)。然而,PPA 闭塞是一项技术要求较高的操作,常常会引起并发症。
在本研究中,我们开发了一种 ICA 注射针,通过 ICA 方便且高效地将干细胞递送至缺血性脑,而无需 PPA 闭塞。我们通过 ICA 注射针(不结扎 PPA)或常规微注射针(结扎 PPA)将亚甲蓝和荧光染料 DiI 标记的人间充质干细胞(DiI-hMSCs)注入大鼠的 ICA,并评估它们的分布。
当注入亚甲蓝时,在注射侧的大脑中发现了明显的蓝色染色,特别是大脑中动脉(MCA)供应区域,但在 PPA 供应区域没有染色。同样,当注入 DiI-hMSCs 时,细胞主要出现在 MCA 供应组织中,其数量与 PPA 结扎的常规微注射针注射相似。此外,用 ICA 针或微注射针注射的 hMSCs 同样改善了梗死脑的功能恢复。
我们的结果表明,ICA 注射针易于使用,能够高效地将细胞递送至大鼠 MCAO 模型的缺血性脑组织。