基础医学与临床 ›› 2014, Vol. 34 ›› Issue (8): 1027-1031.

• 研究论文 • 上一篇    下一篇

神经病理性疼痛对大鼠脊髓背角蛋白磷酸酶1的表达调控作用

陈思1,申乐1,黄宇光2   

  1. 1. 中国医学科学院北京协和医院
    2. 北京协和医院
  • 收稿日期:2013-10-08 修回日期:2014-01-16 出版日期:2014-08-05 发布日期:2014-07-15
  • 通讯作者: 黄宇光 E-mail:garybeijing@163.com
  • 基金资助:
    国家自然科学基金(地区基金);青年科学基金

Neuropathic pain regulated protein phosphatase 1 expression in rat spinal cord dorsal horn

  • Received:2013-10-08 Revised:2014-01-16 Online:2014-08-05 Published:2014-07-15

摘要: 目的 明确双侧坐骨神经松结扎(bCCI)大鼠脊髓背角蛋白磷酸酶1催化亚基β异构体(PPP1CB)的表达水平及其与miR-203之间的关系,以及加巴喷丁的干预效果。方法 48只雌性大鼠,被随机分为Na?ve组、Sham组、bCCI组和bCCI+加巴喷丁组,建立bCCI模型。加巴喷丁干预组分别于术前15min 1次、术后第7天起每日2次,腹腔注射给予加巴喷丁100mg/kg,连续7d。术后第14天处死大鼠,留取脊髓背角(L4~L6)标本,分别利用Real-Time PCR与westernblot技术检测PPP1CB mRNA及蛋白质表达,并进行生物信息学分析。结果 PPP1CB mRNA表达显著下降约0.8倍,而大鼠脊髓背角PPP1CB蛋白表达水平则较对照组和假手术组上升约2倍;加巴喷丁干预组大鼠脊髓背角PPP1CB蛋白表达水平较未干预组有显著回落(P<0.05),但未恢复到对照组和假手术组水平,而PPP1CB mRNA表达水平则较未干预组有显著回升(P<0.05),恢复到与正常对照组、假手术组相同水平;利用生物信息学验证了miR-203对PPP1CB的调控关系。结论 bCCI大鼠脊髓背角PPP1CB蛋白的表达量上升可能受到了miR-203的调控作用,并可能通过多种途径参与了神经病理性疼痛的发生发展。

关键词: 神经病理性疼痛, bCCI, 蛋白磷酸酶1, miR-203, 加巴喷丁

Abstract: Objective This study aimed to clarify the PPP1CB expression level in spinal cord dorsal horn of bCCI rats and its relationship with miR-203, as well as the intervention effect of gabapentin. Method 48 female rats were randomly divided into 4 groups(Na?ve,SHAM,bCCI,bCCI+gabapentin). The interfered group rats were injected 100mg/Kg gabapentin 15min before, 7 days after operation for 7 consecutive days, bid, ip. All rats were sacrificed at POD14. Spinal dorsal horn(L4-L6) were assayed for Real-time PCR, Western-blot to detect mRNA and protein level change and bioinformatics analysis was also involved. Results the PPP1CB protein expression level of spinal cord dorsal horn (L4-L6) significantly increased approximately 2-fold compared with control and sham group, while PPP1CB mRNA expression level was significantly decreased by about 0.8 times. After gabapentin intervention, PPP1CB protein level was changed while PPP1CB mRNA expression was back to normal compared to bCCI group. Meanwhile, bioinformatics tools verified PPP1CB is one of the target genes of miR-203. Conclusion The increase expression of PPP1CB protein in the spinal dorsal horn may play a role in the mechanism of neuropathic pain, and might be regulated by miR-203.

Key words: Neuropathic pain, Bilateral Chronic Constriction Injury(bCCI), protein phosphatase 1, miR-203, gabapentin

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