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延胡索乙素对大鼠慢性神经病理性疼痛的影响 被引量:16

Analgesic effect of levo-tetrahydropalmatine in a rat model of neuropathic pain
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摘要 目的研究延胡索乙素(L-THP)对大鼠坐骨神经慢性压迫损伤神经病理性疼痛(CCI)的镇痛效应及可能的作用机制。方法雄性Wistar大鼠54只,随机均分为:Sham组(S组)、CCI组(C组)和L-THP组(L组)。S组暴露坐骨神经但不结扎,其余组均建立坐骨神经CCI模型。L组大鼠造模后即刻及术后每日腹腔注射L-THP 40mg/kg,连续14d,S组和C组腹腔注射等量生理盐水。三组大鼠造模前1d、术后3、7、14d测试机械痛阈(MWTs)和热痛阈(TWL),处死取海马组织,用Western blot方法检测脂肪酸酰胺水解酶(FAAH)的表达水平。结果术后3、7、14d三组大鼠术后MWTs和TWL显著低于造模前1d,且C、L组明显低于S组(P<0.05);术后3、7、14d时C、L组大鼠海马FAAH表达水平显著高于S组,且L组FAAH的表达水平显著低于C组(P<0.05)。结论 L-THP对大鼠CCI具有镇痛作用,其机制与抑制海马FAAH的表达相关。 Objective To evaluate the analgesic effect of levo-tetrahydropalmatine (L-THP) in sciatic nerve chronic constriction injury (CCL) induced neuropathic pain. Methods Fifty-four Wistar rats were divided into three groups. Sham group (group S), CCI group (group C) and L-THP group (group L). The analgesic effect of L-THP was tested through von Frey filaments and thermal infrared noxious heat stimulator. Western blotting was performed to investigatethe expression of fatty acid amide hydrolase (FAAH) in the hippocampus. Results The threshold mechanical and thermal stimuli at day 3, 7 and 14 were lower than that at day 1, and also both thresholds in groups C and L were higher than those in group S (P〈0.05). The hippocampal expression 0f FAAH at day 3, 7 and 14 were higher in groups C and L than that of group S, but in group C had upregulated expression of FAAT than in group L (P〈0.05). Conclusion L-THP produces analgesic effect on neuropathie pain rats by inhibiting the hippocampal expression of FAAT.
出处 《临床麻醉学杂志》 CAS CSCD 北大核心 2012年第7期705-707,共3页 Journal of Clinical Anesthesiology
关键词 延胡索乙素 神经病理性疼痛 脂肪酸酰胺水解酶 Levo-tetrahydropalmatine Chronic constriction injury Fatty acid amide hydrolase
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  • 1Anand P, Whiteside G, Fowler CJ, et al. Targeting CB2 re- ceptors and the endocannahinoid system for the treatment of pain. Brain Res Re, 2009,60(1):255-266.
  • 2Bennett GJ, Xie YK. A peripheral mononeuropathy in rat that produces disorders of pain sensation like those seen in man. Pain, 1988, 33(1) : 87-107.
  • 3Jhaveri MD, Richardson D, Chapman V. Endocannabinoid metabolism and uptake: novel targets for neuropathic and in- flammatory pain. Br J Pharmacol, 2007, 152(5) :624-632.
  • 4Hwang J, Adamson C, Butler D, et al. Enhancement of en- docannabinoid signaling by fatty acid amide hydrolase inhibi- tion: a neuroprotective therapeutic modality. Life Sci, 2010, 86(15-16) : 615-623.
  • 5金小高,罗爱林,张广雄.三种大鼠神经病理性疼痛模型的制备和效果比较[J].临床麻醉学杂志,2005,21(5):338-340. 被引量:43
  • 6Chu H, Jin G, Friedman E,et al. Recent development in stud- ies of tetrahydroprotoberberines: Mechanism in antinocicep- tion and drug addiction. Cell Mol Neurobiol, 2008, 28 (4) :491-499.
  • 7黄锦煜,方敏,李嫕婧,马勇全,才晓慧.延胡索在三叉神经痛大鼠模型中的镇痛作用研究[J].南方医科大学学报,2010,30(9):2161-2164. 被引量:27

二级参考文献32

  • 1汤法银,聂爱国,李艳玲.中药延胡索的研究进展[J].临床和实验医学杂志,2006,5(2):185-186. 被引量:53
  • 2吴佩盛,黄善定,叶亚菊,孙思源,蒋惠娣.大鼠肠道对左旋延胡索乙素及其消旋体的吸收差异研究[J].药学学报,2007,42(5):534-537. 被引量:14
  • 3Rappaport ZH, Devor M. Trigeminal neuralgia: the role of self-sustaining discharge in the trigeminal ganglion[J]. Pain, 1994, 56:127-318.
  • 4Love S, Coakham HB. Trigeminal neuralgia: pathology and pathogenesis [ J ]. Brain, 2001,124: 2347-60.
  • 5Vos BP, Strassman AM, Maciewicz RJ. Behavioral evidence of trigeminal neuropathic pain following chronic constriction injury to the rat's infraorbital nerve[J]. J Neurosci, 1994,14: 2708-23.
  • 6Quartilho A, Mata HP, lbrahim MM, et al. Inhibition of inflammatory hyperalgesia by activation of peripheral CB2 cannabinoid receptors [J ]. Anesthesiology, 2003, 99: 955-60.
  • 7Hohmann AG, Suplita RL, Bohon NM, et al. An endocannabinoid mechanism for stress-induced an algesia [J]. Nature, 2005, 435:1 108-12.
  • 8Martin WJ, Loo CM, Basbaum AI. Spinal cannabinoids are antiallodynie in rats with persistent inflammation [J]. Pain, 1999, 82: 199-205.
  • 9Elmes LA, Winyard SJ, Medhurst NM, et al. Activation of CB1 and CB2 receptors attenuates the induction and maintenance of inflammatory pain in the rat[J ]. Pain, 2005,118: 327-35.
  • 10Costa B, Siniscalco D, Trovato AE, et al. AM404, an inhibitor of anandamide uptake, prevents pain behaviour and modulates cytokine and apoptotic pathways in a rat model of neuropathie pain [J]. Br J Pharmacol, 2006, 148: 1022-32.

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