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首页> 外文期刊>BioMed research international >Development of a Regenerative Peripheral Nerve Interface for Control of a Neuroprosthetic Limb
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Development of a Regenerative Peripheral Nerve Interface for Control of a Neuroprosthetic Limb

机译:用于控制神经高原肢体的再生外周枢神经界面的发展

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摘要

Background. The purpose of this experiment was to develop a peripheral nerve interface using cultured myoblasts within a scaffold to provide a biologically stable interface while providing signal amplification for neuroprosthetic control and preventing neuroma formation. Methods. A Regenerative Peripheral Nerve Interface (RPNI) composed of a scaffold and cultured myoblasts was implanted on the end of a divided peroneal nerve in rats (n = 25). The scaffold material consisted of either silicone mesh, acellular muscle, or acellular muscle with chemically polymerized poly(3,4-ethylenedioxythiophene) conductive polymer. Average implantation time was 93 days. Electrophysiological tests were performed at endpoint to determine RPNI viability and ability to transduce neural signals. Tissue samples were examined using both light microscopy and immunohistochemistry. Results. All implanted RPNIs, regardless of scaffold type, remained viable and displayed robust vascularity. Electromyographic activity and stimulated compound muscle action potentials were successfully recorded from all RPNIs. Physiologic efferent motor action potentials were detected from RPNIs in response to sensory foot stimulation. Histology and transmission electron microscopy revealed mature muscle fibers, axonal regeneration without neuroma formation, neovascularization, and synaptogenesis. Desmin staining confirmed the preservation and maturation of myoblasts within the RPNIs. Conclusions. RPNI demonstrates significant myoblast maturation, innervation, and vascularization without neuroma formation.
机译:背景。该实验的目的是在支架内使用培养的肌细胞进行外周神经界面,以提供生物稳定的界面,同时提供神经治疗控制和预防神经瘤形成的信号放大。方法。将由支架和培养的肌细胞组成的再生外周神经界面(RPNI)植入大鼠分开的腓神经的末端(n = 25)。支架材料由硅胶网,细胞肌或细胞内肌肉组成,具有化学聚合的聚(3,4-亚乙二氧基噻吩)导电聚合物。平均植入时间为93天。在端点进行电生理试验以确定RPNI的活力和越症神经信号的能力。使用光学显微镜和免疫组织化学检查组织样品。结果。无论支架型,所有植入的RPNI,都保持可行,呈现强大的血管性。从所有RPNIS成功记录了电拍摄活性和刺激的复合肌动作电位。从RPNIS响应于感觉脚刺激,从RPNIS检测到生理迁移电机动作电位。组织学和透射电子显微镜显示成熟的肌肉纤维,没有神经瘤形成,新生血管和突触的轴突再生。 Desmin染色证实了RPNIS内肌细胞的保存和成熟。结论。 RPNI证明了没有神经瘤形成的显着肌细胞成熟,支配和血管化。

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