Role of p38MAPK signaling pathway in rats with phantom limb pain.
10.11817/j.issn.1672-7347.2018.06.003
- Author:
Hui JIANG
1
;
Yongquan CHEN
1
;
Jintao LIU
1
Author Information
1. Department of Anesthesiology, Yijishan Hospital, First Affiliated Hospital of Wannan Medical College, Wuhu Anhui 241000, China.
- Publication Type:Journal Article
- MeSH:
Animals;
Disease Models, Animal;
Enzyme Inhibitors;
pharmacology;
Ganglia, Spinal;
enzymology;
Imidazoles;
pharmacology;
Male;
Mastication;
physiology;
Phantom Limb;
enzymology;
etiology;
physiopathology;
Pyridines;
pharmacology;
Random Allocation;
Rats;
Rats, Sprague-Dawley;
Sciatic Nerve;
injuries;
Self Mutilation;
enzymology;
physiopathology;
Signal Transduction;
Spinal Cord;
enzymology;
p38 Mitogen-Activated Protein Kinases;
antagonists & inhibitors;
metabolism
- From:
Journal of Central South University(Medical Sciences)
2018;43(6):589-593
- CountryChina
- Language:Chinese
-
Abstract:
To investigate the role of p38MAPK signal pathway in spinal cord and dorsal root ganglion (DRG) in rats with phantom limb pain and the effects of specific inhibitors.
Methods: Healthy adult male SD rats (n=48) were cut off one side of the sciatic under anesthesia to establish a model of phantom limb pain. In addition, the healthy rats were taken as a sham group (group S, n=24). The animals were scored by observing the action of chewing (0=no chewing, 13=the worst chewing) after the operation and were sacrificed on the following day after the operation. The successful model of phantom limb pain were randomly divided into 2 groups: a phantom limb pain group (group P, n=24) and a phantom limb pain plus inhibitor group (group P+I, n=24). SB203580 was given to the rat at 0.8 mg/kg on every Monday until the rats were sacrificed, the rest of the rats received an equal amount of saline. Eight rats from each group were randomly taken for the determination of levels of P-p38MAPK in spinal cord and DRG before administration and on the 4th, 6th, 8th weekend following the administration, respectively.
Results: In the sham group, no animal developed chewing. Meanwhile, rats in successful model of phantom limb pain group began chewing from the 2nd day after operation with scores at eight to eleven. The chewing scores in the P+I group were reduced after the treatment. Compared with group S, P-p38MAPK levels were elevated in groups of P and P+I (P<0.05 or P<0.01). Compared with group P, P-p38MAPK level was decreased in the group P+I (P<0.05 or P<0.01).
Conclusion: P38MAPK signal pathway involves in the development of phantom limb pain.
