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Korean J Anesthesiol > Volume 56(3); 2009 > Article
Korean Journal of Anesthesiology 2009;56(3):319-324.
DOI: https://doi.org/10.4097/kjae.2009.56.3.319   
Lidocaine attenuates the expression of ERK1/2 and CREB in a neuropathic pain model of rats.
Jin Deok Joo, Jang Hyeok In, Hong Soo Jung, Yong Shin Kim, Dae Woo Kim, Woo Young Choi, Eun Young Shin, Yeon Soo Jeon
1Department of Anesthesiology and Pain Medicine, St. Vincent Hospital, The Catholic University of Korea, College of Medicine, Seoul, Korea. likewinds@vincent.cuk.ac.kr
2The Research Institute of Medical Science, St. Vincent Hospital, The Catholic University of Korea, College of Medicine, Seoul, Korea.
Abstract
BACKGROUND
In addition to causing the loss of voluntary sensory and motor function, spinal cord injury (SCI) often creates a state of central neuropathic pain. Rats given SCI display increases in the activated form of transcription factors ERK 1/2, p38 MAPK, and CREB in the spinal cord, which correspond to allodynia in a model of neuropathic pain. The current study was designed to determine if lidocaine had an effect on the development of neuropathic pain in response to SCI.
METHODS
Male Sprague Dawley rats were anesthetized and then received a L5-L6 spinal nerve ligation (neuropathic rats). The levels of intracellular cell-signaling protein, ERK 1/2 and CREB were then assessed by western blot analysis of samples collected from a sham operated (control) group, a neuropathic pain and normal saline (NP + NS) group, and a neuropathic pain and 5% lidocaine (NP + Lido) group.
RESULTS
The increased levels of ERK 1/2 and CREB protein that were observed in the neuropathic pain model were reduced by continuous infusion of 5% lidocaine.
CONCLUSIONS
The current results suggest that lidocaine therapy may be an effective method of preventing and treating central neuropathic pain following SCI, and that these effects may occur via the reduced expression of ERK 1/2 and CREB in the intracellular cell-signaling pathway.
Key Words: CREB; ERK 1/2; Intracellular cell-signaling pathway; Lidocaine; Neuropathic pain; Western blots
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