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首页> 外文期刊>Neurology: Official Journal of the American Academy of Neurology >Treatment of stroke in rat with intracarotid administration of marrow stromal cells.
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Treatment of stroke in rat with intracarotid administration of marrow stromal cells.

机译:中风的治疗与intracarotid老鼠骨髓基质细胞。

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OBJECTIVE: To measure the therapeutic efficacy for the treatment of stroke with intra-arterial administration of bone marrow stromal cells (MSC). BACKGROUND: MSC have characteristics of stem and progenitor cells. The hypothesis that MSC injected into the internal carotid artery after stroke enter into ischemic brain and improve neurologic recovery was tested. METHODS: Twenty-five adult Wistar rats were subjected to transient (2-hour) middle cerebral artery occlusion alone (n = 9), or treated with intracarotid arterial injection of 200 microL phosphate-buffered saline (n = 8) or 2 x 10(6) MSC in 200 microL phosphate-buffered saline (n = 8) 1 day after ischemia. MSC were harvested and isolated from additional adult rats and then cultured and labeled with bromodeoxyuridine. Rats were subjected to neurologic functional tests (adhesive-removal, modified neurologic severity scores) before and at 1, 7, and 14 days after middle cerebral artery occlusion. Immunohistochemistry was used to identify cell-specific proteins of bromodeoxyuridine-reactive MSC. RESULTS: Bromodeoxyuridine-reactive cells ( approximately 21% of 2 x 10(6) injected MSC) distributed throughout the territory of the middle cerebral artery by 14 days after ischemia. Some bromodeoxyuridine-reactive cells expressed proteins characteristic of astrocytes and neurons. Rats with intra-arterial transplantation of MSC exhibited improvement on the adhesive-removal test (p < 0.05) and the modified neurologic severity scores (p < 0.05) at 14 days compared with controls. CONCLUSIONS: MSC injected intra-arterially are localized and directed to the territory of the middle cerebral artery, and these cells foster functional improvement after cerebral ischemia.
机译:目的:测量的治疗效果治疗中风的动脉内的骨髓基质细胞(MSC)。干细胞和祖细胞。MSC注入颈内动脉卒中后缺血性脑和进入改善神经功能恢复测试。成人Wistar鼠受到25瞬态(2小时)大脑中动脉闭塞(n = 9),或处理200 microL intracarotid动脉注射磷酸盐(n = 8)或2 x 10 (6)200年MSC microL磷酸盐(n =8)缺血后1天。分离出额外的成年老鼠培养与溴脱氧尿苷标记。受到神经功能测试(adhesive-removal修改神经症状分数)之前,1、7和14天之后大脑中动脉闭塞。免疫组织化学是用于识别特异性的蛋白质bromodeoxyuridine-reactive MSC。Bromodeoxyuridine-reactive细胞(约21%的2 x 10(6)注入MSC)分布整个区域的大脑中动脉缺血后14天。bromodeoxyuridine-reactive细胞表达星形胶质细胞和蛋白质特征神经元。MSC的改进上adhesive-removal测试(p < 0.05)和修改神经严重程度评分(p < 0.05), 14天相比之下,控制。动脉内的本地化和指向大脑中动脉的领土这些细胞培养后功能改进脑缺血。

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