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痛觉过敏的研究进展 被引量:3

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摘要 外周组织炎症或神经损伤常常引起持续性自发痛(spontaneouspain)、痛觉过敏(hyperalgesia)和痛觉超敏(allodynia)等病理性疼痛。持续性自发痛是指在不受任何外来刺激下持续发生的疼痛,痛觉超敏是指非伤害性刺激即可引起的疼痛,
作者 吕兴业
出处 《河北医药》 CAS 2011年第15期2344-2347,共4页 Hebei Medical Journal
关键词 过敏 疼痛
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参考文献16

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  • 3Schmidt AP, Tort AB, Silveira PP, et al. The NMDA antagonistMK-801 induces hyperalgesia and increases CSF excitatory amino acids in rats : reversal by guanosine. Pharmacol Biochem Behav,2009,91:549-553.
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同被引文献60

  • 1邱宇洁,梁宜,方剑乔,房军帆,杜俊英,刘晋.慢性疼痛的JNK信号转导通路机制的研究进展[J].浙江中医药大学学报,2011,35(5):793-796. 被引量:5
  • 2张力军,杨雪琴,吕沙里,李铀.腹式呼吸训练仪对心率及呼吸性窦性心律不齐作用的初步观察[J].北京生物医学工程,2005,24(1):39-41. 被引量:31
  • 3Lee M, Silverman SM, Hansen H, et al. A comprehensive review of opioid-induced hyperalgesia[J]. Pain Physician, 2011, 14(2): 145-161.
  • 4Colvin LA, FaUon MT. Opioid--induced hyperalgesia: a clinical challenge[J].BrJ Anaesth, 2010, 104(2): 125-127.
  • 5Dietis N, Guerrini R, Calo G, et al. Simultaneous targeting of multi- ple opioid receptors: a strategy to improve side-effect profile[J]. Br J Anaesth, 2009, 103(1): 38-49.
  • 6Haugan F, Rygh LJ, Tj#lsen A. Ketamine blocks enhancement of spinal long--term potentiation in chronic opioid treated rats[J]. Acta Anaesthesiol Scand, 2008, 52(5): 681-687.
  • 7Zhao M, Joo DT. Enhancement of spinal N-methyl-D-aspartate receptor function by remifentanil action at delta-opioid receptorsas a mechanism for acute opioid-induced hyperalgesia or tolerance [J]. Anesthesiology, 2008, 109(2): 308-317.
  • 8Van Elstraete AC, Sitbon P, Mazoit JX, et al. Gabapentin prevents delayed and long-lasting hyperalgesia induced by fentanyl in rats [J]. Anesthesiology, 2008, 108(3): 484-494.
  • 9Minville V, Fourcade O, GirolamiJP, et al. Opioid-induced hyper- algesia in a mice model of orthopaedic pain: preventive effect of ket- amine [J]. BrJ Anaesth, 2010, 104(2): 231-238.
  • 10Schmidt AP, Tort AB, Silveira PP, et al. The NMDA antagonist MK--801 induces hyperalgesia and increases CSF excitatory amino acids in rats: reversal by guanosine[J]. Pharmacol Biochem Behav, 2009, 91 (4): 549-553.

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