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A large animal neuropathic pain model in sheep: a strategy for improving the predictability of preclinical models for therapeutic development

机译:绵羊的大型动物神经性疼痛模型:提高治疗开发的临床前模型可预测性的策略

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Background: Evaluation of analgesics in large animals is a necessary step in the development of better pain medications or gene therapy prior to clinical trials. However, chronic neuropathic pain models in large animals are limited. To address this deficiency, we developed a neuropathic pain model in sheep, which shares many anatomical similarities in spine dimensions and cerebrospinal fluid volume as humans.Methods: A neuropathic pain state was induced in sheep by tight ligation and axotomy of the common peroneal nerve. The analgesic effect of intrathecal (IT) morphine was investigated. Interspecies comparison was conducted by analyzing the ceiling doses of IT morphine for humans, sheep, and rats.Results: Peroneal nerve injury (PNI) produced an 86% decrease in von-Frey filament-evoked withdrawal threshold on postsurgery day 3 and the decrease lasted for the 8-week test period. Compared to the pre-injury, sham, and contralateral hindlimb, the IT morphine dose that produces 50% of maximum analgesia (ED50) for injured PNI hindlimb was 1.8-fold larger and Emax, the dose that produces maximal analgesia, was 6.1-fold lower. The sheep model closely predicts human IT morphine ceiling dose by allometric scaling. This is in contrast to the approximately 10-fold lower morphine ceiling dose predicted by the rat spinal nerve ligated or spared nerve injury models.Conclusion: PNI sheep model has a fast onset and shows stable and long-lasting pain behavioral characteristics. Since the antinociceptive properties of IT morphine are similar to those observed in humans, the PNI sheep model will be a useful tool for the development of analgesics. Its large size and consistent chronic pain behavior will facilitate the development and evaluation of surgical intervention and gene therapy. The PNI sheep pain model provides us with the opportunity for multi-species testing, which will improve the success of clinical trials.
机译:背景:在临床试验之前,评估大型动物的镇痛药是开发更好的止痛药或基因疗法的必要步骤。但是,大型动物的慢性神经性疼痛模型有限。为了解决这一缺陷,我们开发了一种绵羊神经病性疼痛模型,该模型与人类在脊柱尺寸和脑脊液量方面具有许多解剖学相似性。方法:通过紧密结扎和腓总神经的轴突切开术在绵羊中诱发了一种神经性疼痛状态。研究鞘内注射吗啡的镇痛作用。通过对人,绵羊和大鼠的IT吗啡上限剂量进行种间比较。结果:术后第3天,腓神经损伤(PNI)使von-Frey丝诱发的撤药阈值降低了86%,并且这种降低持续了下来为期8周的测试期。与受伤前,假手术和对侧后肢相比,对受伤的PNI后肢产生50%最大镇痛(ED50)的IT吗啡剂量要大1.8倍,而产生最大镇痛剂量的Emax是6.1倍。降低。绵羊模型通过异速生长定律密切预测人类IT吗啡的最高剂量。这与大鼠脊髓神经结扎或幸免的神经损伤模型预测的吗啡上限剂量低约10倍相反。结论:PNI绵羊模型起效快,表现出稳定且持久的疼痛行为特征。由于IT吗啡的抗伤害感受特性与人类观察到的相似,因此PNI绵羊模型将成为开发止痛药的有用工具。它的大尺寸和一致的慢性疼痛行为将促进手术干预和基因治疗的发展和评估。 PNI绵羊疼痛模型为我们提供了进行多种物种测试的机会,这将提高临床试验的成功率。

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