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Simulating Pancreatic Neuroplasticity: In Vitro Dual-neuron Plasticity Assay

机译:模拟胰腺神经可塑性:体外双神经元可塑性测定

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摘要

Neuroplasticity is an inherent feature of the enteric nervous system and gastrointestinal (GI) innervation under pathological conditions. However, the pathophysiological role of neuroplasticity in GI disorders remains unknown. Novel experimental models which allow simulation and modulation of GI neuroplasticity may enable enhanced appreciation of the contribution of neuroplasticity in particular GI diseases such as pancreatic cancer (PCa) and chronic pancreatitis (CP). Here, we present a protocol for simulation of pancreatic neuroplasticity under in vitro conditions using newborn rat dorsal root ganglia (DRG) and myenteric plexus (MP) neurons. This dual-neuron approach not only permits monitoring of both organ-intrinsic and -extrinsic neuroplasticity, but also represents a valuable tool to assess neuronal and glial morphology and electrophysiology. Moreover, it allows functional modulation of supplied microenvironmental contents for studying their impact on neuroplasticity. Once established, the present neuroplasticity assay bears the potential of being applicable to the study of neuroplasticity in any GI organ.
机译:神经可塑性是病理条件下肠神经系统和胃肠(GI)神经支配的固有特征。但是,神经可塑性在胃肠道疾病中的病理生理作用仍然未知。可以模拟和调节GI神经可塑性的新型实验模型可以增强对神经可塑性在特定GI疾病(例如胰腺癌(PCa)和慢性胰腺炎(CP))中的贡献的认识。在这里,我们提出了使用新生大鼠背根神经节(DRG)和肠神经丛(MP)神经元在体外条件下模拟胰腺神经可塑性的协议。这种双神经元方法不仅可以监测器官内在和外在的神经可塑性,而且代表了评估神经元和神经胶质形态和电生理的有价值的工具。此外,它允许对所提供的微环境内容物进行功能调节,以研究其对神经可塑性的影响。一旦建立,本发明的神经可塑性测定法就有可能适用于任何胃肠器官中的神经可塑性研究。

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