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首页> 外文期刊>Neurochemical research >Differential roles of phosphorylated AMPA receptor GluR1 subunits at Serine-831 and Serine-845 sites in spinal cord dorsal horn in a rat model of post-operative pain.
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Differential roles of phosphorylated AMPA receptor GluR1 subunits at Serine-831 and Serine-845 sites in spinal cord dorsal horn in a rat model of post-operative pain.

机译:在大鼠术后疼痛模型中,脊髓背角的丝氨酸831和丝氨酸845位点的磷酸化AMPA受体GluR1亚基的差异作用。

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摘要

Previous studies have demonstrated that the enhanced levels of phosphorylated alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionate (AMPA) receptor GluR1 subunits at Serine-831 (pGluR1-Ser-831) and Serine-845 (pGluR1-Ser-845) in the spinal cord dorsal horn are involved in central sensitization of inflammatory pain. However, whether the phosphorylatory regulation of AMPA receptor GluR1 subunits is implicated in the development and maintenance of post-operative pain remains unclear. The current study aims to examine the functional regulation of AMPA receptor GluR1 subunit through its phosphorylation mechanism during the period of post-operative painful events in rats. Our data indicated that the expression of pGluR1-Ser-831 in ipsilateral spinal cord dorsal horn increased significantly at 3 h after incision, then decreased gradually, and returned to the normal level 3 day post-incision. Meanwhile, the expression of pGluR1-Ser-845 and GluR1 in ipsilateral spinal cord dorsal horn remained unchanged. The cumulative pain scores increased at 3 h after incision, gradually decreased afterwards and returned to the baseline values at 4 day after incision and the trend was almost parallel to the expression changes of pGluR1-Ser-831 in spinal dorsal horn. Intrathecal injection of a calcium-dependent protein kinase (PKC) inhibitor, Go6983 (10 muM), significantly reversed the incision-mediated over-expression of pGluR1-Ser-831 in spinal dorsal horn at 3 h after incision and decreased the cumulative pain scores as well. These results indicate that the phosphorylation of GluR1 subunits at Serine-831 and Serine-845 sites might be differentially regulated following surgical procedures and support a neurobiological mechanism of post-operative pain involved in phosphorylation of AMPA subunits GluR1-Ser-831, but not pGluR1-Ser-845. Our study suggests that the therapeutic targeting the phosphorylation regulation of AMPA receptor GluR1 subunit at Serine-831 site would be potentially significant for treating postoperative pain.
机译:先前的研究表明,丝氨酸831(pGluR1-Ser-831)和丝氨酸845(pGluR1-)的磷酸化α-氨基-3-羟基-5-羟基-5-甲基-4-异恶唑丙酸酯(AMPA)受体GluR1亚基的水平提高脊髓背角中的Ser-845)与炎症性疼痛的中枢敏化有关。然而,尚不清楚AMPA受体GluR1亚基的磷酸化调节是否参与术后疼痛的发生和维持。当前的研究旨在通过大鼠术后疼痛事件期间的磷酸化机制来研究AMPA受体GluR1亚基的功能调节。我们的数据表明,切口后3 h,同侧脊髓背角中pGluR1-Ser-831的表达显着增加,然后逐渐降低,并在切口后3天恢复到正常水平。同时,同侧脊髓背角中pGluR1-Ser-845和GluR1的表达保持不变。切开后3 h累积疼痛评分增加,切开后4天逐渐降低,并在切开后4天恢复到基线值,该趋势几乎与pGluR1-Ser-831在脊髓背角的表达变化平行。鞘内注射钙依赖性蛋白激酶(PKC)抑制剂Go6983(10μM),可显着逆转切口3小时后切口介导的pGluR1-Ser-831在脊髓背角的过表达,并降低了累积的疼痛评分也一样这些结果表明,在外科手术后,可能会对Serine-831和Serine-845位点的GluR1亚基进行磷酸化调节,并支持涉及AMPA亚基GluR1-Ser-831磷酸化的术后疼痛的神经生物学机制,但对pGluR1无影响。 -Ser-845。我们的研究表明,靶向丝氨酸831位点AMPA受体GluR1亚基磷酸化调控的治疗方法对于治疗术后疼痛可能具有重要意义。

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