Pre-emptive anti-hyperalgesic effect of electroacupuncture in carrageenan-induced inflammation: Role of nitric oxide

被引:19
作者
Garrido-Suarez, Barbara B. [1 ]
Garrido, Gabino [2 ,3 ]
Marquez, Lucia [2 ]
Martinez, Ioanna [2 ]
Hernandez, Ivones [2 ]
Merino, Nelson [2 ]
Luque, Yilian [2 ]
Delgado, Rene [1 ]
Bosch, Fe [4 ]
机构
[1] Ctr Nacl Coordinador Ensayos Clin, Lab Farmacol Clin, Havana 11600, Cuba
[2] Ctr Quim Farmaceut, Dept Invest Biomed, Havana 16042, Cuba
[3] Univ Catolica Norte, Fac Ciencias, Dept Quim & Farm, Antofagasta, Chile
[4] Clin Dolor Hosp Docente Clin Quirurg 10 Octubre, Havana, Cuba
关键词
Electroacupuncture; Hyperalgesia; Nitric oxide; Carrageenan; EVOKED FIELD POTENTIALS; FOS PROTEIN EXPRESSION; LONG-TERM POTENTIATION; RAT MODEL; SYNTHASE EXPRESSION; CGMP PATHWAY; SPINAL-CORD; PERIPHERAL INFLAMMATION; BEHAVIORAL HYPERALGESIA; SEROTONERGIC RECEPTORS;
D O I
10.1016/j.brainresbull.2009.04.014
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Central sensitization theory has been defined as pivotal for understanding the excitability changes in central neurons following peripheral inflammation or neuropathic injury. Considerable evidence has demonstrated that activation of the N-methyl-D-aspartate (NMDA) subtype of glutamate receptors and subsequent nitric oxide (NO) production are the key in these changes. Consequently, neuromodulator drugs have been developed during the last decades. The electroacupuncture (EA) that acts as biochemical modulator in the spinal horn cord would prevent these changes. The aim of this study was to determine the thermal anti-hyperalgesic effect of EA (10 Hz, 3 mA) and its combination with L-NAME as nitric oxide synthase (NOS) inhibitor in carrageenan-induced hyperalgesia in rats. Also, it investigated the changes in the plasmatic concentrations of NO metabolites. Moreover, the EA combination with sub-effective dose of ketamine as a NMDA antagonist was tested. The EA pre-treatment conducted in unseclated, unrestrained and conscious animals showed a thermal anti-hyperalgesic effect in correspondence with plasmatic increase of NO metabolites. The L-NAME (30 mg/kg) pre-administration decreased significantly the plasmatic concentrations of NO2-/NO3- and suppressed the anti-hyperalgesic effect of EA. The combination of EA with ketamine enhanced the anti-hyperalgesic effect. These data constitute the first report that suggested the participation, at least in part, of the L-arginine-NOS-NO-GMPc pathway activation in anti-hyperalgesic effect of EA in carrageenan-induced inflammation model. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:339 / 344
页数:6
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