Potentiation of Morphine's Antinociception by Group II and Group III Metabotropic Glutamate Receptors Agonists on a Rat Incisional Pain.
10.3344/kjp.2006.19.2.131
- Author:
Chang Mo KIM
1
;
Jeong Il CHOI
;
Hong Beom BAE
;
Seok Jai KIM
;
Sung Tae CHUNG
;
Ok Hwan KIM
;
Myung Ha YOON
Author Information
1. Department of Anesthesiology and Pain Medicine, Chonnam National University Medical School, Gwangju, Korea. mhyoon@chonnam.ac.kr
- Publication Type:Original Article
- Keywords:
drug interaction;
mGluRs;
morphine;
postoperative pain;
spinal cord;
Sprague-Dawley rat
- MeSH:
Animals;
Catheters;
Drug Interactions;
Felodipine;
Humans;
Male;
Morphine;
Morphine Derivatives;
Pain, Postoperative;
Rats*;
Receptors, Metabotropic Glutamate*;
Spinal Cord
- From:The Korean Journal of Pain
2006;19(2):131-136
- CountryRepublic of Korea
- Language:English
-
Abstract:
BACKGROUND: The aim of this study was to clarify the role of spinal groups II and III metabotropic glutamate receptors (mGluRs) with respect to postoperative pain at the spinal level. In addition, the nature of the pharmacological interaction between groups II and III mGluRs agonists and morphine was determined. METHODS: Catheters were inserted into the intrathecal space of male SD rats. To induce postoperative pain, an incision was made in the plantar surface of the hind paw. A pharmacological characteristic for the interaction between groups II and III mGluRs agonists and morphine was evaluated using a fixed-dose analysis. RESULTS: None of intrathecal group II and III mGluRs agonists modified the withdrawal threshold of the incisional pain. The administration of intrathecal morphine resulted in an increase of a dose dependent withdrawal threshold. A fixed-dose analysis revealed that the group III mGluRs agonist, ACPT-III, increased the antinociceptive action of morphine, while the group II mGluRs agonist, APDC, had no effect the antinociception of morphine. CONCLUSIONS: These results suggest that group II and III mGluRs may not play a direct modulatory role in the processing of postoperative pain at the spinal level. However, agonizing group III mGluRs may indirectly contributable to the potentiation of morphines antinociception in the spinal cord. Thus, the combination of morphine and a group III mGluRs agonist may be useful in the management of spinal postoperative pain.
