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吡那地尔对术后持续性疼痛大鼠脊髓JNK/MCP-1释放的影响
作者:朱翔1  曹苏2  秦毅彬2  佘庆2  丁晶晶2  杨建平1 
单位:1. 苏州大学附属第一医院 麻醉科, 江苏 苏州 215006;
2. 南通大学附属医院 麻醉科, 江苏 南通 226001
关键词:术后持续性疼痛 吡那地尔 JNK/MCP-1 脊髓 大鼠 
分类号:R-332;R972.4
出版年·卷·期(页码):2016·35·第五期(678-682)
摘要:

目的:观察吡那地尔(pinacidil)对术后持续性疼痛大鼠脊髓JNK/MCP-1释放的影响。方法:随机将35只大鼠分为正常组(Control组)、假手术组(Sham组)、切割+牵拉皮肤肌肉组(SMIR组)、溶剂+SMIR组(Vehicle组)、吡那地尔+SMIR(Pina组)、吡那地尔+格列苯脲+SMIR组(Pina+Gli组)、格列苯脲+SMIR组(Gli组)等7组。检测各组机械刺激缩足反射痛阈值(MWT),Western blot/ELISA法检测脊髓JNK/MCP-1蛋白表达。结果:(1)与Sham组相比,SMIR组MWT在术后3 d开始降低(P<0.01),并持续21 d(P<0.001)以上;(2)SMIR术后持续显著上调脊髓JNK/MCP-1的表达(P<0.01);(3)鞘内注射吡那地尔显著下调术后SMIR诱导的脊髓JNK/MCP-1表达(P<0.01)和上调MWT(P<0.01),格列苯脲能阻断吡那地尔所引起的上述变化(P<0.05)。结论:吡那地尔能抑制切割及牵拉皮肤肌肉所致的术后持续性疼痛,其机制可能与抑制JNK/MCP-1的上调有关。

Objective:To observe the effect of pinacidil on JNK/MCP-1 expression in spinal cord of a rat model of persistent postoperative pain. Methods:SD rats were divided into 7 groups randomly:control group(Control group), sham operation group (Sham group), skin/muscle incision and retraction group (SMIR group), vehicle+SMIR group (Vehicle group), pinacidil+SMIR (Pina group), pinacidil+ glibenclamide+SMIR group (Pina+Gli group) and glibenclamide+SMIR group (Gli group).The mechanical withdrawal threshold (MWT) of the left hind paw of rats in different group was measured at different time points after the surgery. Western blot/ELISA were used to measure the protein expression level of JNK/MCP-1. Results:(1) Compared with Sham group, MWT in SMIR group was reduced significantly from 3 d after the operation (P<0.01), and lasted for more than 21 d (P<0.001). (2) The protein expression of JNK/MCP-1 were significantly increased after SMIR as compared with the control group(P<0.01). (3) Intrathecal injection of pinacidil attenuated the express of JNK/MCP-1 in the spinal cord (P<0.01) and up-regulated the MWT (P<0.01), which could be blocked by glibenclamide (P<0.05). Conclusion:Pinacidil inhibits the persistent postoperative pain caused by SMIR. The mechanisms may be partly due to the inhibition of JNK/MCP-1 upregulation.

参考文献:

[1] CLARKE H,KATZ J,FLOR H,et al.Genetics of chronic post-surgical pain:a crucial step toward personal pain medicine[J].Can J Anaesth,2015,62(3):294-303.
[2] ZHU X,LIU J Q,GAO Y J,et al.ATP-sensitive potassium channels alleviate postoperative pain through JNK-dependent MCP-1 expression in spinal cord[J].Int J Mol Med,2015,35(5):1257-1265.
[3] GONG L,GAO F,LI J,et al.Oxytocin-induced membrane hyperpolarization in pain-sensitive dorsal root ganglia neurons mediated by Ca(2+)/nNOS/NO/KATP pathway[J].Neuroscience,2015,289c:417-428.
[4] TANG J,ZHU C,LI Z H,et al.Inhibition of the spinal astrocytic JNK/MCP-1 pathway activation correlates with the analgesic effects of tanshinone IIA sulfonate in neuropathic pain[J].J Neuroinflamm,2015,12:57.
[5] FLATTERS S J.Characterization of a model of persistent postoperative pain evoked by skin/muscle incision and retraction(SMlR)[J].Pain,2008,135(1-2):119-130.
[6] SKERRATT S E,WES C W.Ion channel therapeutics for pain[J].Channels,2015,9(6):344-351.
[7] KAWANO T.Potentiation of neuronal ATP-sensitive potassium channels as a novel target for neuropathic pain[J].Nihon Yakurigaku Zasshi,2015,146(1):10-15.
[8] STAURENGO-FERRARI L,ZARPELON A C,LONGHI-BALBINOT D T,et al.Nitroxyl inhibits overt pain-like behavior in mice:role of cGMP/PKG/ATP-sensitive potassium channel signaling pathway[J].Pharmacol Rep,2014,66(4):691-698.
[9] JI R R,BERTA T,NEDERGAARD M.Glia and pain:is chronic pain a gliopathy?[J].Pain,2013,154(Suppl 1):S10-28.
[10] NGUELEFACK T B,FODERN C,NGUELEFACK-MBUYO E P,et al.Enhancement of ATP sensitive potassium current in cat ventricular myocytes by β-adrenoceptor stimulation[J].J Complement Med,2015,474(1):131-145.
[11] AHMADI S,AZARIAN S,EBRAHIMI S S,et al.ATP-sensitive potassium channels and L-type calcium channels are involved in morphine-induced hyperalgesia after nociceptive sensitization in mice[J].Basic Clin Neurosci,2014,5(3):191-198.
[12] GAO Y J,JI R R.Chemokines,neuronal-glial interactions,and central processing of neuropathic pain[J].Pharmacol Ther,2010,126(1):56-68.
[13] ZHU X,CAO S,ZHU M D,et al.Contribution of chemokine CCL2/CCR2 signaling in the dorsal root ganglion and spinal cord to the maintenance of neuropathic pain in a rat model of lumbar disc herniation[J].J Pain,2014,15(5):516-526.

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