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  • 吕虎,徐娟娟,陈辉,许华,孙继虎,蔡志扬,熊源长.活性氧对背根神经节P2X3受体介导的痛信号功能的影响[J].第二军医大学学报,2014,35(4):443-446    [点击复制]
  • LÜ Hu,XU Juan-juan,CHEN Hui,XU Hua,SUN Ji-hu,CAI Zhi-yang,XIONG Yuan-chang.Effect of reactive oxygen species on dorsal root ganglion P2X3 receptor-induced pain signal[J].Acad J Sec Mil Med Univ,2014,35(4):443-446   [点击复制]
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活性氧对背根神经节P2X3受体介导的痛信号功能的影响
吕虎1△,徐娟娟1△,陈辉1,许华1,孙继虎2,蔡志扬3,熊源长1*
0
(1. 第二军医大学长海医院麻醉科, 上海 200433;
2. 第二军医大学基础部生理学教研室, 上海 200433;
3. 武警8710部队医院麻醉科, 莆田 351133
共同第一作者
*通信作者)
摘要:
目的 探讨活性氧(reactive oxygen species,ROS)对P2X3受体介导的神经病理性疼痛作用的影响。方法 用成年雌性SD大鼠建立背根神经节慢性压迫(CCD)神经病理性疼痛模型,建模成功后随机分为4组(每组10只),经腹腔分别注射生理盐水(NS)、PBN 100 mg/kg、PBN 30 mg/kg、PBN 10 mg/kg,给药30 min后,经足底注射P2X3受体特异性激动剂α,β-meATP 50 nmol,体积为50 μL,持续观察注射后15 min内的自发缩足次数和主动悬足时间,并整合计算每2 min内的综合悬足时间(PLTPM)。结果 PBN能够剂量依赖性抑制由α,β-meATP引发的自发性痛行为,与NS组比较,PBN 100 mg/kg组在前6 min内能明显抑制自发性疼痛,差异具有统计学意义(P<0.05),而PBN 30 mg/kg组大鼠仅在2至4 min时间单位表现出差异有统计学意义(P<0.05)。结论 氧自由基清除剂可以有效缓解由CCD模型引发的神经病理性疼痛及P2X3受体激动剂诱发的自发痛,ROS可能作为信号分子参与了P2X3受体介导的痛觉信息的传递。
关键词:  活性氧  P2X3受体  背根神经节慢性压迫  神经病理性疼痛  自由基清除剂
DOI:10.3724/SP.J.1008.2014.00443
投稿时间:2013-10-07修订日期:2013-12-24
基金项目:国家自然科学基金(81070894).
Effect of reactive oxygen species on dorsal root ganglion P2X3 receptor-induced pain signal
LÜ Hu1△,XU Juan-juan1△,CHEN Hui1,XU Hua1,SUN Ji-hu2,CAI Zhi-yang3,XIONG Yuan-chang1*
(1. Department of Anesthesiology, Changhai Hospital, Second Military Medical University, Shanghai 200433, China;
2. Department of Physiology, College of Basic Medical Sciences, Second Military Medical University, Shanghai 200433, China;
3. Department of Anesthesiology, Hospital of No. 8710 Troop of Chinese People's Armed Police Forces, Putian 351133, Fujian, China
Co-first authors.
*Corresponding author.)
Abstract:
Objective To investigate the effect of reactive oxygen species(ROS) on P2X3 receptor-mediated neuropathic pain. Methods Neuropathic pain model was induced in female Sprague Dawley rats by chronic compression of dorsal root ganglia (CCD), and the CCD rats were randomly divided into 4 groups (each group containing 10 rats): Saline group (NS group); PBN 100 mg/kg treatment group; PBN 30 mg/kg treatment group; and PBN 10 mg/kg treatment group. The specific agonist of P2X3 receptor, α, β-meATP (50 nmol in 50 μL), was subcutaneously injected into the plantar surface of the right hind paws of each rat 30 min after PBN or NS injection. The spontaneous paw flinching times and withdrawing time were observed for 15 min after injection and the paw lift time per minute (PLTPM) in every 2 minutes was calculated. Results Pre-treatment with PBN inhibited α, β-meATP-induced spontaneous pain in a dose-dependent manner. Compared with the NS group, PBN 100 mg/kg group significantly inhibited flinching response during the first 6 min (P<0.05), while the rats in PBN 30 mg/kg group only had significantly attenuated flinching response during the second to the fourth minute compared with NS group(P<0.05). Conclusion Oxygen free radical scavenger can effectively alleviate the neuropathic pain caused by CCD and P2X3 receptor agonist-induced spontaneous pain. ROS may act as a messenger in P2X3 receptor-mediated pain signaling transmission.
Key words:  reactive oxygen species  P2X3 receptor  chronic compression of dorsal root ganglia  neuropathic pain  free radical scavengers