首页> 外文期刊>Pharmacology: International Journal of Experimental and Clinical Pharmacology >Modification of rat model of sciatica induced by lumber disc herniation and the anti-inflammatory effect of osthole given by epidural catheterization
【24h】

Modification of rat model of sciatica induced by lumber disc herniation and the anti-inflammatory effect of osthole given by epidural catheterization

机译:腰椎间盘突出症致坐骨神经痛大鼠模型的改良及硬膜外导管置入术对osthole的抗炎作用

获取原文
获取原文并翻译 | 示例
           

摘要

One of the most treatable causes of lower back pain and associated sciatica is lumbar disc herniation (LDH), which is characterized by rupture of the hard outer wall (annulus fibrosis) in a lumbar intervertebral disc. In the current study, we aimed to: (1) develop and characterize a rat model of sciatica induced by LDH, while introducing a novel method of epidural catheterization; (2) use this model to evaluate the effect of osthole on pain due to LDH, and (3) gain insight into the mechanisms through which osthole affects sciatica induced by LDH. The results indicate that our newly developed rat model maintained mechanical allodynia for 28 days without reduction. Moreover, cyclooxygenase-2 (COX-2) and nitric oxide synthase (NOS) were overexpressed in the associated inflammatory response, which is consistent with clinical manifestations of the disease. We then used this model to study the effect and mechanisms through which osthole affected pain due to LDH. Our study suggests that osthole is capable of reversing hyperalgesia due to LDH, potentially through modulation of activity of COX-2 and NOS, two important proteins for the exacerbation of pain due to LDH. Finally, a molecular modeling simulation showed that osthole has unique binding capabilities to both NOS and COX-2. As the model-induced mechanical hyperalgesia response was consistent, and the position of the catheter tip and the extension/spreading of the drug in the epidural space were reliable, this study developed an improved model to study remedies for sciatic pain. Moreover, our studies demonstrate that osthole may be a feasible treatment for the reduction of pain due to hyperalgesia.
机译:腰椎间盘突出症(LDH)是下腰痛和相关性坐骨神经痛最可治疗的原因之一,其特征是腰椎间盘硬质外壁破裂(纤维环化)。在当前的研究中,我们旨在:(1)建立并表征由LDH诱导的坐骨神经痛的大鼠模型,同时引入一种新的硬膜外导管插入方法; (2)使用该模型评估osthole对LDH引起的疼痛的影响,以及(3)深入了解osthole影响LDH诱导的坐骨神经痛的机制。结果表明,我们新开发的大鼠模型可保持机械性异常性疼痛28天,且无减少。此外,环氧合酶2(COX-2)和一氧化氮合酶(NOS)在相关的炎症反应中过表达,这与该疾病的临床表现是一致的。然后,我们使用该模型研究了蛇床子素影响LDH引起的疼痛的作用和机制。我们的研究表明,蛇床子素能够逆转LDH引起的痛觉过敏,可能是通过调节COX-2和NOS的活性来实现的,这两种蛋白可加剧LDH引起的疼痛。最后,分子建模仿真表明,蛇床子素对NOS和COX-2具有独特的结合能力。由于模型引起的机械性痛觉过敏反应是一致的,并且导管尖端的位置和药物在硬膜外腔中的扩展/扩散是可靠的,因此本研究开发了一种改进的模型来研究坐骨神经痛的治疗方法。此外,我们的研究表明,蛇床子素可能是减轻痛觉过敏引起的疼痛的可行方法。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号