首页> 外文期刊>Neuroimmunomodulation >p38/MAPK inhibitor modulates the expression of dorsal horn GABA(B) receptors in the spinal nerve ligation model of neuropathic pain.
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p38/MAPK inhibitor modulates the expression of dorsal horn GABA(B) receptors in the spinal nerve ligation model of neuropathic pain.

机译:p38 / MAPK抑制剂调节神经性疼痛的脊髓神经结扎模型中背角GABA(B)受体的表达。

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BACKGROUND: Neuropathic pain is one of the most challenging clinical problems due to a lack of understanding the mechanisms. Recent studies have suggested that activated microglia in spinal cord may play a vital role in nerve injury-induced neuropathic pain, but the exact mechanisms have not been fully determined. METHODS: First, we investigated the changes of dorsal horn GABA(B) receptor 1 (R1) expression in spinal nerve ligation rats. Second, we explored whether activated microglia contributed to such neuron changes by intrathecal administration of the p38 inhibitor, SB203580. RESULTS: In this study, we found a dynamic change of GABA(B)R1a protein expression after spinal nerve ligation, and the peripheral nerve injury-induced downregulation of GABA(B)R1a expression in the spinal dorsal horn could be prevented by intrathecal administration of a p38/MAPK inhibitor SB203580. CONCLUSIONS: Our results provide valuable information for a better understanding of neuropathic pain and may contribute to developing effective treatments in future studies.
机译:背景:由于缺乏对机制的了解,神经性疼痛是最具挑战性的临床问题之一。最近的研究表明,脊髓中激活的小胶质细胞可能在神经损伤引起的神经性疼痛中起着至关重要的作用,但确切的机制尚未完全确定。方法:首先,我们研究了脊髓结扎大鼠背角GABA(B)受体1(R1)表达的变化。其次,我们探讨了鞘内注射p38抑制剂SB203580是否激活了小胶质细胞,从而促进了这种神经元的变化。结果:在这项研究中,我们发现脊髓神经结扎后GABA(B)R1a蛋白表达的动态变化,鞘内给药可预防周围神经损伤引起的脊髓背角GABA(B)R1a表达下调p38 / MAPK抑制剂SB203580的合成。结论:我们的结果为更好地了解神经性疼痛提供了有价值的信息,并可能有助于在未来的研究中开发有效的治疗方法。

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