Neuropathic pain and temporal expression of preprodynorphin, protein kinase C and N-methyl-D-aspartate receptor subunits after spinal cord injury

被引:26
作者
Labombarda, Florencia [1 ,2 ]
Florencia Coronel, Maria [1 ,3 ]
Jose Villar, Marcelo [3 ]
Federico De Nicola, Alejandro [1 ,2 ]
Laura González, Susana [1 ,2 ]
机构
[1] Consejo Nacl Invest Cient & Tecn, Lab Bioquim Neuroendocrina, Inst Biol & Med Expt, RA-1033 Buenos Aires, DF, Argentina
[2] Univ Buenos Aires, Fac Med, Buenos Aires, DF, Argentina
[3] Univ Austral, Fac Ciencias Biomed, Buenos Aires, DF, Argentina
基金
奥地利科学基金会;
关键词
Neuropathic pain; Spinal cord injury; NMDA receptor; Mechanical allodynia; Preprodynorphin; Protein kinase C;
D O I
10.1016/j.neulet.2008.09.062
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Central neuropathic pain is refractory to conventional treatment and thus remains a therapeutic challenge. In this work, we used a well-recognized model of central neuropathic pain to evaluate time-dependent expression of preprodynorphin (ppD), protein kinase C gamma (PKC gamma) and NMDA receptor (NMDAR) subunits NR1, NR2A and NR2B, all critical players in nociceptive processing at the spinal level. Male Sprague-Dawley rats were subjected to spinal hemisection at T13 level and sham-operated rats were included as control animals. The development of hindpaw mechanical allodynia was assessed using the von Frey filaments test. Real time RT-PCR was employed to determine the relative mRNA levels of NMDAR subunits, ppD and PKC gamma in the dorsal spinal cord 1, 14 and 28 days after injury. Our results show that, coincident with the allodynic phase after injury, there was a strong up-regulation of the mRNAs coding for ppD, PKC gamma and NMDAR subunits in the dorsal spinal cord caudal to the injury site. The present study provides further evidence that these molecules are involved in the development/maintenance of central neuropathic pain and thus could be the target of therapeutic approaches. (C) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:115 / 119
页数:5
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