Edaravone inhibits pain sensitivity through decreasing pJNK expression in dorsal root ganglia and spinal cord in rats with spinal nerve ligated
10.3724/SP.J.1008.2009.00898
- Author:
Xing-Zhi LIAO
1
Author Information
1. Department of Anesthesiology
- Publication Type:Journal Article
- Keywords:
Edaravone;
Free radical scavenger;
Neuropathic pain;
pJNK;
Spinal nerve liagation
- From:
Academic Journal of Second Military Medical University
2010;30(8):898-902
- CountryChina
- Language:Chinese
-
Abstract:
Objective: To investigate the effect of edaravone on the pain sensitivity in rats with spinal nerve ligated and to probe into the related mechanism. Methods: Male adult SD rats were randomly divided into 3 groups: a sham (Sham) group, a spinal nerve ligation (SNL) group and edaravone(Eda) group. The paw withdrawal mechanical threshold(PWMT) was measured before and after ligation (once daily for 7 days). Rats were sacrificed at specified time points and the left(operation side) L4 and L5 dorsal root ganglia(DRG) and the right (control side) L5 DRG were obtained and immunostained to observe the changes of pJNK in DRG neurons and spinal cords, so as to observe the effect of edaravone on pJNK. Results: Edaravone can reduce the mechanical hyperalgesia induced by spinal nerve ligation. Immunostaining showed that the SNL group had an increased pJNK in the ipsilateral DRG neurons (L5) 24 hours after ligation; double immunofluorescence indicated that the expression of pJNK in the ipsilateral spinal astrocytes was increased 3 days after ligation. Edaravone can reduce pJNK expression in DRG neurons and spinal cords at corresponding time points. Conclusion: Edaravone can relieve the neuropathic pain induced by spinal nerve ligation, and the mechanism might be related to the inhibition of pJNK expression in DRG neurons and spinal cords.
