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间质干细胞经动脉内给药在双重毒素诱导的多系统萎缩动物模型中的可行性和疗效。

Feasibility and Efficacy of Intra-Arterial Administration of Mesenchymal Stem Cells in an Animal Model of Double Toxin-Induced Multiple System Atrophy.

机构信息

Department of Neurology, Yonsei University College of Medicine, Seoul, South Korea.

Severance Biomedical Science Institute, Yonsei University, Seoul, South Korea.

出版信息

Stem Cells Transl Med. 2017 May;6(5):1424-1433. doi: 10.1002/sctm.16-0438. Epub 2017 Mar 13.

Abstract

Multiple system atrophy (MSA) is a sporadic neurodegenerative disease of the central and autonomic nervous system. Because no drug treatment consistently benefits MSA patients, neuroprotective strategy using mesenchymal stem cells (MSCs) has a lot of concern for the management of MSA. In this study, we investigated the safety and efficacy of intra-arterial administration of MSCs via internal carotid artery (ICA) in an animal model of MSA. The study was composed of feasibility test using a ×10 and ×50 of a standard dose of MSCs (4 × 10 MSCs) and efficacy test using a ×0.2, ×2, and ×20 of the standard dose. An ultrasonic flow meter and magnetic resonance imaging (MRI) showed that no cerebral ischemic lesions with patent ICA blood flow was were observed in animals receiving a ×10 of the standard dose of MSCs. However, no MSA animals receiving a ×50 of the standard dose survived. In efficacy test, animals injected with a ×2 of the standard dose increased nigrostriatal neuronal survival relative to a ×0.2 or ×20 of the standard dose. MSA animals receiving MSCs at ×0.2 and ×2 concentrations of the standard dose exhibited a significant reduction in rotation behavior relative to ×20 of the standard dose of MSCs. Cerebral ischemic lesions on MRI were only observed in MSA animals receiving a ×20 of the standard dose. The present study revealed that if their concentration is appropriate, intra-arterial injection of MSCs is safe and exerts a neuroprotective effect on striatal and nigral neurons with a coincidental improvement in motor behavior. Stem Cells Translational Medicine 2017;6:1424-1433.

摘要

多系统萎缩(MSA)是一种中枢和自主神经系统的散发性神经退行性疾病。由于没有药物治疗能持续改善 MSA 患者的病情,因此使用间充质干细胞(MSCs)的神经保护策略受到了广泛关注,可用于 MSA 的治疗。在这项研究中,我们通过颈内动脉(ICA)在 MSA 动物模型中研究了经动脉内给予 MSCs 的安全性和疗效。该研究包括使用标准剂量 MSC 的 10 倍和 50 倍(4×10 MSC)进行的可行性测试,以及使用标准剂量的 0.2 倍、2 倍和 20 倍进行的疗效测试。超声流量计和磁共振成像(MRI)显示,接受标准剂量 MSC 的 10 倍的动物的 ICA 血流无脑缺血性病变。然而,没有接受标准剂量 MSC 的 50 倍的 MSA 动物存活。在疗效测试中,与标准剂量的 0.2 倍或 20 倍相比,注射标准剂量的 2 倍 MSC 的动物的黑质纹状体神经元存活增加。接受标准剂量 MSC 的 0.2 和 2 倍浓度的 MSA 动物的旋转行为显著减少,而接受标准剂量 MSC 的 20 倍浓度的动物则没有。只有接受标准剂量 MSC 的 20 倍的 MSA 动物的 MRI 上出现脑缺血性病变。本研究表明,如果其浓度适当,经动脉内注射 MSC 是安全的,对纹状体和黑质神经元具有神经保护作用,并伴有运动行为的改善。《干细胞转化医学》2017 年;6:1424-1433。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a583/5442709/35ea19495ba2/SCT3-6-1424-g001.jpg

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