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Decellularized peripheral nerve grafts by a modified protocol for repair of rat sciatic nerve injury

机译:通过改性方案进行脱细胞外周神经移植物,用于修复大鼠坐骨神经损伤

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Studies have shown that acellular nerve xenografts do not require immunosuppression and use of acellular nerve xenografts for repair of peripheral nerve injury is safe and effective. However, there is currently no widely accepted standard chemical decellularization method. The purpose of this study is to investigate the efficiency of bovine-derived nerves decellularized by the modified Hudson’s protocol in the repair of rat sciatic nerve injury. In the modified Hudson’s protocol, Triton X-200 was replaced by Triton X-100, and DNase and RNase were used to prepare accelular nerve xenografts. The efficiency of bovine-derived nerves decellularized by the modified Hudson’s protocol was tested in vitro by hematoxylin & eosin, Alcian blue, Masson’s trichrome, and Luxol fast blue staining, immunohistochemistry, and biochemical assays. The decellularization approach excluded cells, myelin, and axons of nerve xenografts, without affecting the organization of nerve xenografts. The decellularized nerve xenograft was used to bridge a 7 mm-long sciatic nerve defect to evaluate its efficiency in the repair of peripheral nerve injury. At 8 weeks after transplantation, sciatic function index in rats subjected to transplantation of acellular nerve xenograft was similar to that in rats undergoing transplantation of nerve allograft. Morphological analysis revealed that there were a large amount of regenerated myelinated axons in acellular nerve xenograft; the number of Schwann cells in the acellular nerve xenograft was similar to that in the nerve allograft. These findings suggest that acellular nerve xenografts prepared by the modified Hudson’s protocol can be used for repair of peripheral nerve injury. This study was approved by the Research Ethics Committee, Research and Technology Chancellor of Guilan University of Medical Sciences, Iran (approval No. IR.GUMS.REC.1395.332) on February 11, 2017.
机译:研究表明,无细胞神经异种移植物不需要免疫抑制和使用细胞神经异种移植物用于修复周围神经损伤是安全有效的。但是,目前没有广泛接受的标准化学脱细胞化方法。本研究的目的是探讨由改良的哈德森在大鼠坐骨神经损伤修复方面脱牛衍生神经的效率。在改进的Hudson的方案中,Triton X-200被Triton X-100取代,并且DNase和RNase用于制备加速神经异种移植物。通过修饰的哈德逊的方案脱粗的牛衍生神经的效率,通过苏木精和曙红,阿尔西亚蓝,马隆的三明治,Luxol快速蓝色染色,免疫组化和生物化学测定,体外测试。脱细胞化方法排除了神经异种移植物的细胞,髓鞘和轴突,而不会影响神经异种移植物的组织。脱细胞神经异种移植物用于弥合7mm长的坐骨神经缺陷,以评估其在周围神经损伤修复方面的效率。移植后8周,经受细胞神经异种移植移植的大鼠的大鼠中的坐骨函数指数类似于暴动神经同种异体移植的大鼠中的大鼠。形态学分析表明,在细胞神经异种移植物中存在大量再生的脊髓轴突;细胞神经异种移植物中的氏氏细胞的数量与神经同种异体移植物中的施旺细胞的数量相似。这些研究结果表明,由改性的哈德逊的方案制备的细胞神经异种移植物可用于修复周围神经损伤。本研究于2017年2月11日,桂兰医学科学大学研究伦理委员会,桂兰医学院研究和技术校长研究综合法委员会批准。

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