Weil Institute of Critical Care Medicine, Rancho Mirage, CA, USA.
Crit Care Med. 2008 Nov;36(11 Suppl):S486-91. doi: 10.1097/ccm.0b013e31818a8ff0.
Allogeneic bone marrow mesenchymal stem cells were previously shown to improve myocardial function when administered intravenously after resuscitation from cardiac arrest in rats. Coincidental evidence of improved brain function prompted the present study.
Prospective, randomized, controlled study.
University-affiliated research institute.
Male Sprague-Dawley rats.
Using an established model in 20 male Sprague-Dawley rats in which 6 mins of untreated cardiac arrest was followed by cardiopulmonary resuscitation, animals were randomized to receive 5 x 10(6) mesenchymal stem cells labeled with PKH26 in phosphate buffer solution or phosphate buffer solution alone as a placebo at 2 hrs after restoration of spontaneous circulation. The stem cells or buffer diluent were injected into a catheter advanced from the jugular vein into the right atrium.
Outcome measurements in addition to 35-day survival included somatosensor testing of capability for removal of an adhesive patch applied to both front paws, testing of motor function using a rotating cylinder, and observational scoring of the severity of neurologic impairment. Labeled mesenchymal stem cells were subsequently identified and counted in 5 microm sections obtained from defined sites in the harvested brain. Immunohistochemistry was used to identify neural cells differentiation of mesenchymal stem cells. Adhesive removal, motor function test, neurologic severity score, and 35-day survival were each significantly improved in comparison with control animals. Labeled mesenchymal stem cells were identified in the hippocampus, cortex, pons, medulla, and cerebellum and expressed protein markers phenotypic neural cells.
Mesenchymal stem cells injected into the right atrium of rats after resuscitation from cardiac arrest were identified in brains harvested 35 days later. Brain function was significantly improved. Accordingly, venous injection of mesenchymal stem cells after cardiopulmonary resuscitation has promise of minimizing the severity of postresuscitation neurologic impairment.
先前的研究表明,同种异体骨髓间充质干细胞在大鼠心脏骤停复苏后经静脉给药可改善心肌功能。偶然的证据表明其也能改善脑功能,促使我们进行了本研究。
前瞻性、随机、对照研究。
大学附属研究所。
雄性 Sprague-Dawley 大鼠。
在 20 只雄性 Sprague-Dawley 大鼠中建立了一个模型,该模型中,未经治疗的心脏骤停 6 分钟后,进行心肺复苏,动物随机分为两组,在自主循环恢复后 2 小时,分别接受 5×10(6)个标记有 PKH26 的间充质干细胞或磷酸盐缓冲液作为安慰剂。将干细胞或缓冲液稀释剂通过从颈静脉推进到右心房的导管注入。
除 35 天存活率外,还进行了体感测试(评估移除贴在前爪上的粘性贴片的能力)、旋转圆筒测试(评估运动功能)和神经损伤严重程度的观察评分。随后在收获的大脑中从定义部位获得的 5 μm 切片中鉴定和计数标记的间充质干细胞。免疫组织化学用于鉴定间充质干细胞的神经细胞分化。与对照组相比,粘附去除、运动功能测试、神经严重程度评分和 35 天存活率均显著提高。在海马体、皮质、脑桥、延髓和小脑均鉴定到标记的间充质干细胞,并表达了神经细胞表型的蛋白标记物。
在心脏骤停复苏后将间充质干细胞注入大鼠右心房,35 天后在收获的大脑中可鉴定到间充质干细胞。大脑功能明显改善。因此,心肺复苏后静脉注射间充质干细胞有望减轻复苏后神经损伤的严重程度。